Version 2/2021

®

Pflanzliche Wirkstoffe und AnalytikI

Product List 2021

Reference Substances Natural Compounds

PHYTOPLAN Diehm & Neuberger GmbH Im Neuenheimer Feld 515 D-69120 Heidelberg Germany

Phone: 0049 62 21 / 40 13 47

Fax: 0049 62 21 / 43 76 64 email: [email protected] Internet: www.Phytoplan.com

Dear customer,

We are pleased to introduce our new catalogue for the year 2021. Therein you will find many new products and also a greater range in the qualities of the compounds differing in the degree of purity and the documents delivered. Please decide which item is the proper choice for your purpose.

Catalogue of natural compounds In our catalogue we have listed the substances which are near-term available. Often you can choose a definite degree of purity and extent of documentation (see column ' documents delivered '). The substances are mostly of high purity and are available as identification standards or HPLC standards dependent on the extent of the documentation. Some compounds are offered also in larger quantities with a lower degree of purity. All substances are delivered with an individual certificate of analysis which shows the purity by means of HPLC DAD. In addition you will find specific data of the substance together with a DAD ultraviolet spectrum. Due to their purity (usually 97.0 – 99.0 %) the reference substances in our catalogue are suitable for ambitious applications. On customers request the extent of the current documentation can be individually expanded and adapted. Please check which specific requirement of the documentation for your application (e.g. for authorization or registration, HPLC standard, working standard etc.) is demanded.

Reference substances This class of substances is characterized by high purity (mostly greater 98.0 %). The certificate of analysis delivered contains both chromatographic measurements of the purity with TLC, HPLC-DAD and/or GC/MS and spectroscopic measurements like NMR, UV, IR, MS inclusive the spectra and data interpretation. The extent of the certificate of analysis is listed in the catalogue on the column 'documents delivered'. On customers request also further analytical investigations (content of water, solvent residues) can be performed. If you are interested we can transfer you more information about discrete substances. Dependent on the quantity ordered the delivery time may be prolonged. The availability of these substances however is warranted for longer periods. On demand we can extend the certificates of analysis which are designed only for HPLC standards with further documents so that these substances can also be characterized as identification standards.

HPLC-standards

We supply these substances with a purity predominantly in the range of 95.0 – 99.0 %. The current purity is indicated in the certificate of analysis together with a HPLC DAD chromatogram and UV spectrum.

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Bulkware Some compounds are offered with a lower degree of purity but in larger units and at a more favourable price. For degrees of purity not specified in the catalogue we can make you an offer. In all cases you are provided with a certificate with HPLC DAD chromatogram.

Isolation on request If you are interested in one or several compounds from a definite plant we will study the feasibility and make you an offer in accordance with the individual costs. The requirements of the documentation and the specification will be made by your defaults. In our laboratories we use all established chromatographic separation media and separation techniques. This enables us to produce even difficult accessible substances in multigram quantities. The likewise existing classical-chemical laboratory equipment facilitates also synthetic alternatives to pure isolation.

Purification on request

If you have a substance which is not sufficiently pure for your application we can clean it up in accordance with your specification. Use our broad experience with different classes of substances and separation problems. Please request for an offer.

Shipment costs

Dependent on the country we must charge your parcel with different effective shipment costs. We will inform you about the costs on demand or in the order confirmation.

Bank connection PHYTOPLAN Diehm & Neuberger GmbH (company) Bank account: Heidelberger Volksbank eG (bank) Kurfürstenanlage 8 (street) D-69115 Heidelberg (postal code, city) Germany Bank Identifier Code (BIC): GENODE61HD1 interBank-Acc. No. (IBAN): DE67 6729 0000 0022 5906 77 VAT ID: DE190955227

For inquiry please contact: Mr. Dr. Michael Diehm or Mr. Dr. Karl Neuberger Phone: 0049 6221 401347, Fax: 0049 6221 437664, email: [email protected], Website: www.phytoplan.de

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List of available compounds A Cimiracemoside C Acetoxyvalerenic acid Cimiracemoside F 6-O-Acetylacteoside Cnicin 3-O-Acetyl--boswellic acid Coptisine chloride 3-O-Acetyl--boswellic acid Cucurbitacin I 3-O-Acetyl-9,11-dehydro--boswellic acid Curcumin 7-O-Acetylintermedine 3-arabinoside chloride 7-O-Acetylintermedine N-oxide Cyanidin chloride 3-O-Acetyl-11-keto--boswellic acid Cyanidin 3-galactoside chloride 7-O-Acetyllycopsamine hydrochloride Cyanidin 3-glucoside chloride 7-O-Acetyllycopsamine N-oxide Cyanidin 3-(6”-malonylglucoside) Actein Cyanidin 3-rutinoside chloride Acteoside Cyanidin 3-sambubioside chloride Agnuside Cyanidin 3-sophoroside chloride Aloe-Emodin Cyanin chloride Aloenin A Cynarin Amarogentin Cytisine Amentoflavon D Anagyrinhydrochlorid Angustifoline chloride Delphinidin 3,5-diglucoside chloride Apigenin 7-glucoside Delphinidin 3-galactoside chloride Delphinidin 3-glucoside chloride Aristolochic acid mixture Delphinidin 3-rutinoside chloride Aristolochic acid sodium salt Delphinidin 3-sambubioside chloride Aristolochic acid I 27-Deoxyactein Aristolochic acid II 26-Deoxycimicifugoside Aristolochic acid C Dhurrin Aristolochic acid D (+)-Dihydroquercetin Aucubin Azadirachtin E Echimidine B Echimidine Echimidine Echimidine Bergamottin Echimidine Betulin Echimidine Betulinic aic Echimidine (-)-Bilobalide Echimidine N-oxide -Boswellic acid Echinacoside -Boswellic acid Echinatine Echinatine N-oxide C -Elemonic acid Elenolic acid 2-O-glucoside Eleutheroside B Eleutheroside E Emodin (Frangula-) Catalpol Englerin A (-)-Catechin Englerin B (+)-Catechin (-)-Epicatechin Cephaeline dihydrobromide (-)-Epicatechin 3-gallate -Chaconine (-)-Epigallocatechin Chamaemeloside (-)-Epigallocatechin 3-gallate Epiprogoitrin Chelidonine (Z)-Erucifoline Chlorogenic acid (Z)-Erucifoline N-oxide Cichoric acid Eupatorin Cimiaceroside A Europine hydrochloride Cimigenol-3-O-arabinoside Europine N-oxide Cimigenol-3-O-xyloside Cimiracemoside A

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List of available compounds F I Frangulin (A + B) Frangulin A Indicine hydrochloride Frangulin B Indicine N-oxide Integerrimine G Integerrimine N-oxide (-)-Gallocatechin Intermedine [6]-Gingerol Intermedine N-oxide [8]-Gingerol Isoacteoside [10]-Gingerol Ginkgolide A Isoquercitrin Ginkgolide B Ginkgolide C Isoverbascoside Ginkgolic acids RN Glucoalyssin Isoxanthohumol Glucoarabin Glucobarbarin J Glucoberteroin Jacobine Glucobrassicanapin Jacobine N-oxide Glucobrassicin Jacoline Glucocamelinin Jacoline N-oxide Glucocapparin Jaconine Glucocheirolin Jaconine N-oxide Glucoerucin Glucohesperin K Glucohirsutin Glucoiberin Kaempferol 3-glucoside Glucolimnanthin 11-Keto--boswellic acid Glucomoringin Kuromanin chloride Gluconapin Gluconasturtiin L Glucoraphanin Lasiocarpine Glucoraphasatin E/Z mixture Lasiocarpine N-oxide Glucoraphenin Leiocarposide Glucotropaeolin Linarin Lucidin 3-primveroside H Lupanine hydrochloride Hamamelitannin Lutein Harpagide Harpagoside Luteolin 7-glucoside Hederacoside C Lycopene Hederagenin Lycopsamine -Hederin Lycopsamine N-oxide Heliosupine Heliosupine N-oxide M Heliotridine (-)-Maackiain Heliotridine N-oxide chloride Heliotrine Malvidin 3-galactoside chloride Heliotrine N-oxide Malvidin 3-glucoside chloride Hesperetin chloride Hesperidin Manassantin A Homoorientin Manassantin B Homoglucocamelinin Merenskine 7-Hydroxyaristolochic acid I Merenskine N-oxide 4-Hydroxyglucobrassicin Merepoxine 13-Hydroxylupanine Merepoxine N-oxide 18-Hydroxyspartioidine 4-Methoxyglucobrassicin Hydroxytyrosol 11-(Methylsulfinyl)undecylglucosinolate Hydroxyvalerenic acid Monocrotaline Hyperforin/Adhyperforin DCHA salt Monocrotaline N-oxide Hypericin Morindin Hypericin sodium salt Multiflorine page 5 

List of available compounds N Narciclasine Sceleratine N-oxide Naringenin Senecionine Naringin Senecionine N-oxide Neoglucobrassicin Seneciphylline Seneciphylline N-oxide O Senecivernine chloride Senecivernine N-oxide Oleuropein Senkirkin -Onocerin Sennoside A Sennoside A1 Otonecin Sennoside B Sennoside C P [6]-Shogaol Pectolinarigenin Silybin Pectolinarin Sinalbin chloride Sinalbin potassium salt Pelargonidin 3,5-diglucoside chloride Sinigrin Pelargonidin 3-glucoside chloride -Solanine Penduletin Spartioidine chloride Spiraeoside Peonidin 3,5-diglucoside chloride Sutherlandioside B Peonidin 3-glucoside chloride Sutherlandioside D 3-glucoside chloride Picroside II T Primin (+)-Taxifolin Primulaverin Trichodesmine Primverin Thesinine Thesinine 4‘-glucoside Progoitrin Trifolirhizin Protopine Pseudohypericin U Umckalin Ursolic acid Usaramine Q Usaramine N-oxide Quercetin 3-galactoside V Quercetin 3-glucoside Valerenic acid Verbascoside Vescalagin R -Viniferin Retronecine Retronecine N-oxide Vitexin 2‘‘-O-rhamnoside Retrorsine Retrorsine N-oxide W Rhein Rhein 8-O-glucoside Wogonoside Riddelliine Riddelliine N-oxide X Rinderine Xanthohumol Rinderine N-oxide Rosmarinic acid Ruberythric acid Ryanodine

S Sceleratine

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List of available compounds We have a special focus on the following Pyrrolizidine Alkaloids categories of compounds: 7-O-Acetylintermedine Anthocyans 7-O-Acetylintermedine N-oxide 7-O-Acetyllycopsamine hydrochloride Cyanidin 3-arabinoside chloride 7-O-Acetyllycopsamine N-oxide Cyanidin chloride Echimidine Cyanidin 3-galactoside chloride Echimidine N-oxide Cyanidin 3-glucoside chloride Echinatine Cyanidin 3-(6”-malonylglucoside) Echinatine N-oxide Cyanidin 3-rutinoside chloride Erucifoline Cyanidin 3-sambubioside chloride Erucifoline N-oxide Cyanidin 3-sophoroside chloride Europine hydrochloride Cyanin chloride Europine N-oxide Delphinidin chloride Heliotridine Delphinidin 3,5-diglucoside chloride Heliosupine Delphinidin 3-galactoside chloride Heliosupine N-oxide Delphinidin 3-glucoside chloride Heliotridine N-oxide Delphinidin 3-rutinoside chloride Heliotrine Delphinidin 3-sambubioside chloride Heliotrine N-oxide Kuromanin chloride 18-Hydroxyspartioidine Malvidin chloride Indicine hydrochloride Malvidin 3-galactoside chloride Indicine N-oxide Malvidin 3-glucoside chloride Integerrimine Malvin chloride Integerrimine N-oxide Oenin chloride Intermedine Pelargonidin chloride Intermedine N-oxide Pelargonidin 3,5-diglucoside chloride Jacobine Pelargonidin 3-glucoside chloride Jacobine N-oxide Peonidin chloride Jacoline Peonidin 3,5-diglucoside chloride Jacoline N-oxide Peonidin 3-glucoside chloride Jaconine Petunidin 3-glucoside chloride Jaconine N-oxide Lasiocarpine Lasiocarpine N-oxide Glucosinolates Lycopsamine Epiprogoitrin Lycopsamine N-oxide Glucoalyssin Merenskine Glucoarabin Merenskine N-oxide Glucobarbarin Merepoxine Glucoberteroin Merepoxine N-oxide Glucobrassicanapin Monocrotaline Glucobrassicin Monocrotaline N-oxide Glucocamelinin Otonecin Glucocapparin Retronecine Glucocheirolin Retronecine N-oxide Glucoerucin Retrorsine Glucohesperin Retrorsine N-oxide Glucohirsutin Riddelliine Glucoiberin Riddelliine N-oxide Glucolimnanthin Rinderine Glucomoringin Rinderine N-oxide Gluconapin Sceleratine Gluconasturtiin Sceleratine N-oxide Glucoraphanin Senecionine Glucoraphasatin E/Z-mixture Senecionine N-oxide Glucoraphenin Seneciphylline Glucotropaeolin Seneciphylline N-oxide Homoglucocamelinin Senecivernine 4-Hydroxyglucobrassicin Senecivernine N-oxide 4-Methoxyglucobrassicin Senkirkine 11-(Methylsulfinyl)undecylglucosinolate Spartioidine Neoglucobrassicin Trichodesmine Progoitrin Thesinine Sinigrin Thesinine 4’-glucoside Sinalbin Usaramine Sinalbin potassium salt Usaramine N-oxide page 7 

Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

Acacetin 20 mg 130 OCH3 HPLC-DAD Linarigenin, 5,7-Dihydroxy-4‘-methoxyflavone with UV-Spectrum HO O from Robinia pseudoacacia 50 mg 265 Art. 3209.99 >99.0 % OH O [480-44-4] C16H12O5 Mr 284.26

O Acetoxyvalerenic acid HPLC-DAD (2 25 mg 365 CH3 H3C O H from Valeriana officinalis methods), Art. 4402.RS >99.0 % TLC (2 methods), 1H-NMR, 13C-NMR CH [81397-67-3] or [84638-55-1] 3 CH3 - (with C17H24O4 Mr 292.37 COOH Interpretation), UV, IR, MS, solvent residue, water O Acetoxyvalerenic acid HPLC-DAD 10 mg 170 CH3 H3C O H from Valeriana officinalis with UV-Spectrum 25 mg 278 Art. 4402.99 >99.0 % CH [81397-67-3] or [84638-55-1] 3 CH3 C17H24O4 Mr 292.37 COOH

 6-O-Acetylacteoside HPLC-DAD 10 mg 115 OAc O 6-O-Acetylverbascoside HO O with UV-Spectrum O O O OH from Harpagophytum procumbens 20 mg 199 HO OH H3C O HO OH HO HO Art. 6100.99 >99.0 % 50 mg 395 [441769-43-3] C31H38O16 Mr 666.64

H3C CH3 3-O-Acetyl--boswellic acid HPLC-DAD 5 mg 140 H (3,4)-3-Acetoxyolean-12-ene-23-oic acid with UV-Spectrum from Boswellia serrata 10 mg 235 H C CH3 CH 3 3 H CH3 Art. 5154.99 >99.0 % 20 mg 398 AcO H [89913-60-0] HOOC CH 3 C32H50O4 Mr 498.73

 CH3 3-O-Acetyl--boswellic acid HPLC-DAD 5 mg 135 H3C (3,4)-3-Acetoxyurs-12-ene-23-oic acid H with UV-Spectrum from Boswellia serrata 10 mg 210 H3C CH3 CH3 Art. 5151.99 >99.0 % 20 mg 375 H CH 3 [5968-70-7] AcO H C32H50O4 Mr 498.73 HOOC CH3

 3-O-Acetyl-9-11-dehydro--boswellic acid CH3 HPLC-DAD 5 mg 230 H3C (3,4)-3-Acetoxyurs-10,12-diene-23-oic acid with UV-Spectrum H Acetyl--boswellic acid 10 mg 398 H C CH from Boswellia serrata 3 3 CH3 CH3 Art. 5156.98 >98.0 % AcO H [122651-20-1] HOOC CH3 C32H48O4 Mr 496.71

7-O-Acetylintermedine 5 mg 210 HPLC-DAD H3C CH3 from Symphytum officinale with UV-Spectrum 10 mg 365 O CH3 AcO H Art. 6276.95 >95.0 % OH O OH [74243-01-9]

N C17H27NO6 Mr 341.40

By ordering a single compound in the 5fold or 10fold quantity in one packing unit you will get a discount of 10 percent or 15 percent respectively. Page 8 

Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

H C CH 7-O-Acetylintermedine N-oxide 5 mg 210 3 3 HPLC-DAD from Symphytum officinale with UV-Spectrum O CH3 10 mg 365 AcO H Art. 6277.95 >95.0 % OH OH O [685132-59-6] + N C17H27NO7 Mr 357.40 - O

 CH3 H C 3-O-Acetyl-11-keto--boswellic acid 5 mg 126 3 HPLC-DAD H with UV-Spectrum O 3-Acetoxyurs-12-ene-11-keto-23-oic acid from Boswellia serrata 10 mg 198 H3C CH3 CH3 H CH3 Art. 5153.99 >99.0 % 20 mg 344 AcO H [67416-61-9] HOOC CH3 C32H48O5 Mr 512.73

H C CH 7-O-Acetyllycopsamine hydrochloride 5 mg 210 3 3 HPLC-DAD Lycopsamine 1‘-acetate hydrochloride with UV-Spectrum O CH3 from Symphytum 10 mg 365 AcO H OH OH O Art. 6350.95 >95.0 % + N [ - ] - H Cl C17H28ClNO6 Mr 377.86

H3C CH3 7-O-Acetyllycopsamine N-oxide 5 mg 210 HPLC-DAD from Symphytum with UV-Spectrum O CH3 10 mg 365 AcO H OH O OH Art. 6273.97 >97.0 % + [685132-58-5] N - C17H27NO7 Mr 357.40 O

Actein HPLC-DAD (2 10 mg 330 H3C AcO O OH Shengmating CH3 O methods), O from Cimicifuga racemosa 20 mg 580 CH3 TLC, 1H-NMR, 13C-NMR CH3 Art. 3506.RS >99.0 % Xyl-O [18642-44-9] - (with Interpretation), H3C CH3 C H O M 676.84 IR, MS, Melting point 37 56 11 r Actein HPLC-DAD 5 mg 165 H3C AcO O OH from Cimicifuga racemosa CH3 O with UV-Spectrum O 10 mg 215 CH3 Art. 3506.99 >99.0 % CH3 [18642-44-9] 20 mg 410 Xyl-O C H O M 676.84 H3C CH3 37 56 11 r 50 mg 920

 Acteoside 20 mg 320 OH HPLC-DAD, TLC, O HO O Verbascoside 1 13 O H-NMR, C-NMR O O OH 50 mg 640 HO OH from Paulownia tormentosa - (with H3C O HO OH HO Interpretation), HO Art. 6101.RS >98.0 % UV, IR, MS [61276-17-3]

C29H36O15 Mr 624.59

 Acteoside 10 mg 135 OH HPLC-DAD O HO O Verbascoside O with UV-Spectrum O O OH 20 mg 235 HO OH from Paulownia tormentosa H3C O HO OH HO HO Art. 6101.98 >98.0 % 50 mg 475 [61276-17-3] C29H36O15 Mr 624.59

By ordering a single compound in the 5fold or 10fold quantity in one packing unit you will get a discount of 10 percent or 15 percent respectively. Page 9 

Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 Agnuside 10 mg 126 HO HO H HPLC-DAD 10-p-Hydroxybenzoylaucubin with UV-Spectrum 20 mg 230 from Vitex agnus castus O H O CH2 O-Glu Art. 2102.99 >99.0 % O [11027-63-7] C22H26O11 Mr 466.44

 Aloe-Emodin 20 mg 120 OHO OH HPLC-DAD 1,8-Dihydroxy-3-(hydroxymethyl)-anthraquinone with UV-Spectrum synthetic 50 mg 265

CH2OH Art. 3714.99 >99.0 % O [481-72-1] C15H10O5 Mr 270.23

 HO OGlu Aloenin A HPLC-DAD 10 mg 135 from Aloe arborescens with UV-Spectrum O O 20 mg 248 Art. 4105.99 >99.0 % CH3 [38412-46-3] 50 mg 515 C19H22O10 Mr 410.38 OCH3

 OH Amarogentin HPLC-DAD 10 mg 150 O from Gentiana lutea with UV-Spectrum O 20 mg 275 H H HO OH Art. 2122.99 >99.0 % O OH [21018-84-8] O OO OH C29H30O13 Mr 586.54 O OH

Amentoflavone  OH HPLC-DAD 10 mg 100 OH I3',II8-Biapigenin, Didemethylginkgetin HO O with UV-Spectrum from Ginkgo biloba 20 mg 175 O OH OH O Art. 3285.99 >99.0 % O [1617-53-4] HO C H O M 538.47 30 18 10 r

- Anagyrine hydrochloride 10 mg 300 H Cl HPLC-DAD + from Anagyris foetida N with UV-Spectrum Art. 6325.97 >97.0 % N H [5973-07-9] O C15H21ClN2O Mr 280.80

Angustifoline HPLC-DAD 5 mg 245 H NH CH2 Jamaicensine with UV-Spectrum from Lupinus angustifolius N H Art. 6320.95 >95.0 % O [550-43-6] C14H22N2O Mr 234.34

 Apigenin OH HPLC-DAD 20 mg 100 4',5,7-Trihydroxyflavone with UV-Spectrum HO O from Chamomillae romana 50 mg 205 Art. 3205.99 >99.0 % 100 mg 390 OH O [520-36-5] C15H10O5 Mr 270.23

By ordering a single compound in the 5fold or 10fold quantity in one packing unit you will get a discount of 10 percent or 15 percent respectively. Page 10 

Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 Apigenin OH HPLC-DAD 50 mg 130 4',5,7-Trihydroxyflavone with UV-Spectrum HO O from Chamomillae romana Art. 3205.97 >97.0 % OH O [520-36-5] C15H10O5 Mr 270.23

OH Apigenin 7-glucoside HPLC-DAD (2 20 mg 285 Glu-O O , Cossmetin, 7-Glucosylapigenin methods) from Chamomillae romana TLC, 1H-NMR, 13C- 50 mg 560 NMR OH O 100 mg 820 Art. 3207.RS >99.0 % - (with Interpretation), [578-74-5] UV, IR, MS, Melting C21H20O10 Mr 432.38 point

OH Apigenin 7-glucoside HPLC-DAD 20 mg 150 Glu-O O Apigetrin, Cossmetin, 7-Glucosylapigenin with UV-Spectrum from Chamomillae romana 50 mg 340

OH O Art. 3207.99 >99.0 % [578-74-5] C21H20O10 Mr 432.38

OH Apigenin 7-glucoside HPLC-DAD 100 mg 150 Glu-O O Apigetrin, Cossmetin, 7-Glucosylapigenin with UV-Spectrum from Chamomillae romana

OH O Art. 3207.97 >97.0 % [578-74-5] C21H20O10 Mr 432.38

OH Apiin HPLC-DAD 10 mg 182 Apioside, Apigenin 7-apiosylglucoside Api-Glu-O O with UV-Spectrum from Petroselinum crispum 20 mg 325

OH O Art. 3244.98 >98.0 % [26544-34-3] C26H28O14 Mr 564.50

 O COOH Aristolochic acid HPLC-DAD 500 mg 230 mixture of Aristolochic acids with Aristolochic NO with UV-Spectrum O 2 acid I and II as main components from Aristolochia clematitis Art. 4610.96 >96.0 % R [67123-64-2]

 O COONa Aristolochic acid Sodium salt HPLC-DAD 250 mg 205 mixture of Aristolochic acids I und II as NO with UV-Spectrum O 2 main components, Sodium salt 500 mg 350 from Aristolochia clematitis

R Art. 4615.96 >96.0 % [10190-99-5]

 O COOH Aristolochic acid I HPLC-DAD 20 mg 185 Aristolochic acid A, Aristolochin with UV-Spectrum NO O 2 from Aristolochia clematitis 50 mg 365 Art. 4611.99 >99.0 % [313-67-7] OCH3 C17H11NO7 Mr 341.28

By ordering a single compound in the 5fold or 10fold quantity in one packing unit you will get a discount of 10 percent or 15 percent respectively. Page 11 

Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 O COOH Aristolochic acid I HPLC-DAD 250 mg 290 Aristolichic acid A, Aristolochin with UV-Spectrum NO 500 mg 510 O 2 from Aristolochia clematitis

Art. 4611.96 >96.0 % [313-67-7] OCH 3 C17H11NO7 Mr 341.28

 O COOH Aristolochic acid II HPLC-DAD 20 mg 230 Aristolochic acid B, Noraristolochic acid with UV-Spectrum NO 50 mg 470 O 2 from Aristolochia clematitis

Art. 4613.99 >99.0 % [475-80-9] C16H9NO6 Mr 311.25

 Aristolochic acid II 250 mg 430 O COOH HPLC-DAD Aristolochic acid B, Noraristolochic acid with UV-Spectrum NO2 from Aristolochia clematitis O Art. 4613.96 >96.0 % [475-80-9] C16H9NO6 Mr 311.25

 O COOH Aristolochic acid C HPLC-DAD 10 mg 250 Aristolochic acid IIIa with UV-Spectrum NO 20 mg 470 O 2 from Aristolochia clematitis

Art. 4612.98 >98.0 % [4849-90-5] HO C16H9NO7 Mr 327.25

 O COOH Aristolochic acid D HPLC-DAD 10 mg 300 Aristolochic acid IVa NO with UV-Spectrum O 2 from Aristolochia clematitis 20 mg 560

Art. 4614.96 >96.0 % [17413-38-6] HO OCH3 C17H11NO8 Mr 357.27

 Aristolochic acid I, 7-Hydroxy- see 7-Hydroxyaristolochic aicd I

 HO H Aucubin HPLC-DAD (2 20 mg 225

Rhinanthin, Aucuboside methods), TLC, 1H- from Aucuba japonica NMR, 13C-NMR 50 mg 395 O - (with H Art. 2101.RS >99.0 % HOH2C Interpretation), O-Glu [479-98-1] UV, IR, MS, Melting C H O M 346.33 15 22 9 r point

 Aucubin HPLC-DAD 20 mg 125 HO H Rinanthin, Aucuboside with UV-Spectrum from Aucuba japonica 50 mg 255 O H Art. 2101.99 >99.0 % HOH2C O-Glu [479-98-1] C15H22O9 Mr 346.33

CH3 Azadirachtin 1 mg 125 O O HPLC-DAD O OH OHCH3 O from Azadirachta indica H3C O with UV-Spectrum O O 5 mg 340 CH 3 O O Art. 4501.97 >97.0 % CH3 H C O OH 10 mg 605 3 [11141-17-6] O O C35H44O16 Mr 720.72 H3C O

By ordering a single compound in the 5fold or 10fold quantity in one packing unit you will get a discount of 10 percent or 15 percent respectively. Page 12 

Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

Baicalein HPLC-DAD 20 mg 160 5,6,7-Trihydroxyflavone HO O with UV-Spectrum from Scutellaria baicalensis 50 mg 320

HO Art. 3204.99 >99.0 % OH O [491-67-8] C15H10O5 Mr 270.24

Baicalin HPLC-DAD 20 mg 136

HOOC O 5,6,7-Trihydroxyflavone 7-glucuronide with UV-Spectrum HO OH O O Baicalein-7--D-glucopyranosiduronic acid 50 mg 270 OH from Scutellaria baicalensis HO OH O Art. 3206.99 >99.0 % [21967-41-9] C21H18O11 Mr 446.37  Bergamottin HPLC-DAD 20 mg 120 5-Geranoxypsoralen with UV-Spectrum O from Oleum bergamottae 50 mg 240

Art. 2114.99 >99.0 % O O O [7380-40-7] C21H22O4 Mr 338.42

CH3 Betulin HPLC-DAD 1 g 130 H2C Lup-20(29)-ene-3,28-diol, Betulinol H with UV-Spectrum from Betula pendula H3C CH3 H CH2OH

H CH3 Art. 5142.97 >97.0 % HO [473-98-3] H C30H50O2 Mr 442.73

CH3 Betulinic acid HPLC-DAD 20 mg 100 H2C H 3ß-Hydroxy-lup-20(29)-ene-28-acid with UV-Spectrum from Platanus acerifolia 50 mg 210 H3C CH3 H COOH

H CH3 Art. 5144.97 >97.0 % HO [472-15-1] H C30H48O3 Mr 456.71

 (-)-Bilobalide 10 mg 105 OOO O HPLC-DAD O from Ginkgo biloba with UV-Spectrum 20 mg 180 OH O OH Art. 4255.98 >98.0 % CH C 3 [33570-04-6] CH 3 C H O M 326.30 H3C 15 18 8 r

H3C CH3 -Boswellic acid 5 mg 135 HPLC-DAD H (3,4)-3-Hydroxyolean-12-ene-23-oic acid with UV-Spectrum 10 mg 230 H3C CH3 CH3 from Boswellia serrata

H CH3 Art. 5155.99 >99.0 % 20 mg 398 HO H [471-66-9] HOOC CH3 C30H48O3 Mr 456.73

 CH3 -Boswellic acid 5 mg 131 H3C HPLC-DAD H (3,4)-3-Hydroxyurs-12-ene-23-oic acid with UV-Spectrum from Boswellia serrata 10 mg 208 H3C CH3 CH3 H CH3 Art. 5150.99 >99.0 % 20 mg 375 HO H [631-69-6] HOOC CH3 C30H48O3 Mr 456.73

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

Caftaric acid HPLC-DAD 10 mg 207 OH 2-Caffeoyltartaric acid with UV-Spectrum HOOC O 20 mg 369 OH from Echinacea pallida O HO COOH Art. 6106.98 >98.0 % [67879-58-7] C13H12O9 Mr 312.24

OH HO OH OH Castalagin 10 mg 200 HPLC-DAD OH from Castanea sativa with UV-Spectrum O O O OH 20 mg 374 O OH O O Art. 3311.97 >97.0 % HO O O O OH O [24312-00-3] HO OH C41H26O26 Mr 934.63 OH OH HO OH OH

 Castalin 10 mg 198 OH HPLC-DAD OH OH from Castanea sativa with UV-Spectrum O O 20 mg 365 HO O O O OH O Art. 3310.97 >97.0 % HO OH [19086-75-0] OH OH HO OH C27H20O18 Mr 632.43 OH

 Casticin 10 mg 140 HPLC-DAD OH Vitexicarpin with UV-Spectrum 20 mg 245 H3CO O from Vitex agnus castus OCH3

H3CO OCH3 Art. 3238.99 >99.0 % OH O [479-91-4] C19H18O8 Mr 374.32

HO  H Catalpol HPLC-DAD 20 mg 140 from Picrorhiza kurrooa with UV-Spectrum O 50 mg 280 O Art. 2109.99 >99.0 % H [2415-24-9] HOH2C OGlc C15H22O10 Mr 362.33

OH (-)-Catechin HPLC-DAD 10 mg 175 HO O (-)-Catechol, 3,3',4',5,7-Pentahydroxyflavan with UV-Spectrum OH from Acacia catechu 20 mg 290 OH OH Art. 3303.97 >97.0 % [18829-70-4] C15H14O6 Mr 290.27

OH (+)-Catechin HPLC-DAD 20 mg 120 (+)-Catechol, Cianidanol, (+)-Cyanidanol HO O with UV-Spectrum OH from Acacia catechu 50 mg 242 OH Art. 3304.99 >99.0 % OH [154-23-4] C15H14O6 Mr 290.27

H3CO Cephaeline dihydrobromide HPLC-DAD 20 mg 130 x 2HBr N Desmethylemetin dihydrobromide with UV-Spectrum H3CO H 50 mg 210 O CH3 from Ipecacuanha CH3 H Art. 6304.97 >97.0 % OCH3 HN [6014-81-9] OH C28H38N2O4 x 2HBr Mr 628.43

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 H3C H CH3 -Chaconine 5 mg 149 H HPLC-DAD N H C H 3 H CH3 from Solanum tuberosum with UV-Spectrum CH2OH H H O O 10 mg 265 OH O OH O Art. 6208.98 >98.0 % O CH3 [20562-03-2] OH OH OH O C45H73NO14 Mr 852.04 CH3

OH OH

CH3 Chamaemeloside 10 mg 200 HO O HPLC-DAD Apigenin-7-[6''-(3-hydroxy-3-methylglutaryl)glucoside] O CH3 O with UV-Spectrum OH HO O from Anthemis nobilis HO O O OH OH Art. 3208.98 >98.0 % OH O [173356-77-9] C27H28O14 Mr 576.51

OH HO OH Chebulinic acid HPLC-DAD 10 mg 290 O OH HO Eutannin with UV-Spectrum O O O OH 20 mg 550 HO O from Terminalia chebula O O

O O HO O Art. 3316.97 >97.0 % OH O HOOC HO OH [18942-26-2] O C H O M 956.68 O OH 41 32 27 r

Chelidonine 20 mg 129 O HPLC-DAD Stylophorin with UV-Spectrum H3C O N from Chelidonium majus 50 mg 261 H O H Art. 6302.98 >98.0 % O OH [476-32-4] C20H19NO5 Mr 353.37

Chlorogenic acid 20 mg 92 HO COOH HPLC-DAD O 3-Caffeoylquinic acid with UV-Spectrum HO 50 mg 127 O OH from green coffee beans OH HO Art. 6107.99 >99.0 % [327-97-9] C16H18O9 Mr 354.31

O Cichoric acid HPLC-DAD 10 mg 181 HO O COOH Chicoric acid, 2,3-Dicaffeoyltartaric aicd with UV-Spectrum from Echinacea pallida 20 mg 345 HO O COOH HO Art. 6105.98 >98.0 % O [70831-56-0] HO C22H18O12 Mr 474.38

H3C CH3 H3C O Cimiaceroside A HPLC-DAD 2 mg 290 CH3 OH from Cimicifuga racemosa with UV-Spectrum O OH 5 mg 675 H CH3 Art. 3511.97 >97.0 % O O H OH [210643-83-7] H3C CH3 HO C35H54O9 Mr 618.81 OH

H3C Cimigenol-3-O-arabinoside HPLC-DAD 5 mg 219 H CH3 O Cimigenol-3-O-α-L-arabinopyranoside, H with UV-Spectrum CH3 H 10 mg 384 O OH Cimiracemoside C, Cimicifugoside M CH3 OH CH3 HO O from Cimicifuga racemosa O H OH H3C CH3 OH Art. 3508.98 >98.0 % [256925-92-5] C35H56O9 Mr 620.83

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

H3C Cimigenol-3-O-xyloside HPLC-DAD 5 mg 170 H CH3 O Cimigenol-3-O-β-D-xylopyranoside, H with UV-Spectrum CH3 H 10 mg 275 O OH Cimigenoside, Cimigoside CH3 OH CH3 from Cimicifuga racemosa O O H OH H3C CH3 HO Art. 3509.98 >98.0 % OH [27994-11-2] C35H56O9 Mr 620.83

Cimiracemoside A see Cimiracemoside A

Cimiracemoside C see Cimigenol-3-O-arabinoside

CH3 H3C H C O CH3 Cimiracemoside F 2 mg 280 O O 3 HPLC-DAD

CH3 OH Cimiracemoside A with UV-Spectrum O OH 5 mg 650 H from Cimicifuga racemosa CH3 O O H OH Art. 3510.98 >98.0 % H3C CH3 HO OH [264875-61-8] C37H56O11 Mr 676.38

OH Cnicin 10 mg 135 O HPLC-DAD from Cnicus benedictus CH3 with UV-Spectrum O OH 20 mg 228 Art. 2113.98 >98.0 % CH2 [24394-09-0] O HO C20H26O7 Mr 378.42 O

Coptisine chloride 10 mg 125 O HPLC-DAD Bis(methylendioxy)protoberberin chloride with UV-Spectrum O from Chelidonium majus 20 mg 221

O + - N Cl Art. 6301.99 >99.0 % O [6020-18-4] or [3486-66-6] (cation) C19H14NClO4 Mr 355.78

Cucurbitacin I 5 mg 115 O HPLC-DAD HO Elatericin B with UV-Spectrum 10 mg 210 O H OH from Iberis amara H OH HO Art. 5138.99 >99.0 % 20 mg 375 O [2222-07-3] C30H42O7 Mr 514.66

O Curcumin HPLC-DAD 10 mg 110 H3CO Diferuloylmethane with UV-Spectrum from Curcuma longa 20 mg 200 HO O H3CO Art. 4320.98 >98.0 % [458-37-7] HO C21H20O6 Mr 368.39

OH Cyanidin 3-arabinoside chloride 5 mg 141 - OH HPLC-DAD Cl from Aronia melanocarpa with UV-Spectrum + HO O 10 mg 230 Art. 5023.95 >95.0 %

O-Ara [57186-11-5] or [111613-04-8] OH C20H19ClO10 Mr 454.82

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

OH Cyanidin chloride HPLC-DAD 20 mg 145 OH Cl- Cyanidol with UV-Spectrum HO O+ from Rosa centifolia

OH Art. 5003.97 >97.0 % [528-58-5] OH C15H11ClO6 Mr 322.70

OH Cyanidin 3-galactoside chloride 5 mg 130 - OH HPLC-DAD Cl with UV-Spectrum + HO O from Vaccinium vitis-idaea 10 mg 200

O-Gal Art. 5022.97 >97.0 % OH [27661-36-5] C21H21ClO11 Mr 484.84

OH Cyanidin 3-glucoside chloride HPLC-DAD 10 mg 126 Cl Kuromanin chloride, Asterin with UV-Spectrum HO O OH from Rubus fruticosus 20 mg 240 OGlu Art. 5002.97 >97.0 % OH [7084-24-4] C21H21ClO11 Mr 484.84

OH

OH Cyanidin 3-(6”-malonylglucoside) HPLC-DAD 5 mg 230 O O HO O+ - Cyanidin 3-O-(6”-O-malonyl-β-D-glucoside) with UV-Spectrum O O H from Zea mays 10 mg 400 O H O H HO OH OH H OH H Art. 5027.95 >95.0 % [171828-62-9] C24H22O14 Mr 534.43

Cyanidin 3-rutinoside chloride 10 mg 105 OH HPLC-DAD Cl Antirhinin, Keracyanin with UV-Spectrum HO O 20 mg 175 OH from Ribes nigrum

ORutinose Art. 5004.97 >97.0 % [18719-76-1] OH C27H31ClO15 Mr 630.98

OH _ OH Cl Cyanidin 3-sambubioside chloride HPLC-DAD 5 mg 175 HO O+ Sambicyanin chloride with UV-Spectrum OH H from Hibiscus sabdariffa 10 mg 310 O O HO H OH O OH H H H H Art. 5029.97 >97.0 % O H OH H H [33012-73-6] H H HO C26H29ClO15 Mr 616.95 OH

OH OH _ Cyanidin 3-sophoroside chloride 5 mg 195 Cl HPLC-DAD HO O+ with UV-Spectrum fromRubus idaeus 10 mg 350 OH O OH O OH HO Art. 5031.97 >97.0 % OH O O [18376-31-3] or [38820-68-7] OH HO C27H31ClO16 Mr 646.96 OH

Cyanin chloride 20 mg 141 OH HPLC-DAD Cl Cyanidin 3,5-diglucoside chloride with UV-Spectrum HO O 50 mg 285 OH from Rosa centifolia

OGlu Art. 5001.98 >98.0 % OGlu [2611-67-8]

C27H31ClO16 Mr 646.96

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

Cyanin chloride HPLC-DAD 100 mg 178 OH Cl Cyanidin 3,5-diglucoside chloride with UV-Spectrum HO O from Rosa centifolia OH

OGlu Art. 5001.95 >95.0 % OGlu [2611-67-8] C27H31ClO16 Mr 646.96

HO Cynarin HPLC-DAD, TLC, 10 mg 242 O 1,3-Dicaffeoylquinic acid, 1,5 Dicaffeylquinic acid 1 13 HO H-NMR, C-NMR 20 mg 395 O COOH from Cynara scolymus - (with Interpretation), O UV, IR, MS, Melting HO Art. 6103.RS >99.0 % 50 mg 725 O OH point OH [1182-34-9]; [30964-13-7]; [1884-23-7] HO C25H24O12 Mr 516.46

HO Cynarin 10 mg 125 O HPLC-DAD HO 1,3-Dicaffeoylquinic acid, 1,5 Dicaffeylquinic acid with UV-Spectrum O COOH 20 mg 240 O from Cynara scolymus HO O OH Art. 6103.99 >99.0 % 50 mg 500 OH HO [1182-34-9]; [30964-13-7]; [1884-23-7] C25H24O12 Mr 516.46

Cytisine 20 mg 120 HPLC-DAD NH Laburnin with UV-Spectrum 50 mg 250 N from Laburnum anagyroides

O Art. 6204.98 >98.0 % [485-35-8] C11H14N2O Mr 190.25

OH Delphinidin chloride 10 mg 130 OH HPLC-DAD Cl- from Vaccinium myrtillus or Vitis vinifera with UV-Spectrum HO O+ 20 mg 238 OH Art. 5015.97 >97.0 % OH [528-53-0] OH C15H11ClO7 Mr 338.70

OH Delphinidin 3,5-diglucoside chloride 10 mg 220 HPLC-DAD - OH Cl Delphin chloride with UV-Spectrum HO O+ OH from Punica granatum

O-ß-D- Art. 5030.97 >97.0 % [17670-06-3] O-ß-D-Glucose C27H31ClO17 Mr 662.99

OH Delphinidin 3-galactoside chloride 5 mg 145 HPLC-DAD - OH Cl Empetrin with UV-Spectrum HO O+ 10 mg 225 OH from Vaccinium myrtillus

O-Gal Art. 5017.95 >95.0 % 20 mg 410 OH [28500-00-7] C21H21ClO12 Mr 500.84

OH Delphinidin 3-glucoside chloride 10 mg 165 HPLC-DAD OH Cl- with UV-Spectrum 20 mg 310 HO O+ from Vaccinium myrtillus or Vitis vinifera OH Art. 5018.95 >95.0 % O-Glu [6906-38-3] OH C H ClO M 500.84 21 21 12 r

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

OH Delphinidin 3-rutinoside chloride 10 mg 150 HPLC-DAD - OH Delphinidin 3-glucorhamnoside, with UV-Spectrum Cl 20 mg 245 HO O+ from Ribes nigrum OH Art. 5009.97 >97.0 % O-Rutinosyl [15674-58-5] OH C H ClO M 646.98 27 31 16 r

OH Delphinidin 3-sambubioside chloride 5 mg 180 _ OH HPLC-DAD Cl + from Hibiscus sabdariffa HO O with UV-Spectrum OH 10 mg 315 OH H O Art. 5028.95 >95.0 % O HO H OH O OH H [53158-73-9] H H H O H OH C26H29ClO16 Mr 632.95 H H H H HO OH

27-Deoxyactein HPLC-DAD (2 10 mg 485 23-epi-26-Deoxyactein methods), from Cimicifuga racemosa TLC (2 methods), 50 mg 2.000 1H-NMR, 13C-NMR Art. 3505.RS >99.0 % - (with Interpretation), [264624-38-6] IR, MS, hr-MS, C H O M 660.84 37 56 10 r Melting point

27-Deoxyactein HPLC-DAD 5 mg 200 23-epi-26-Deoxyactein with UV-Spectrum from Cimicifuga racemosa 10 mg 340 Art. 3505.99 >99.0 % 20 mg 600 [264624-38-6]

C37H56O10 Mr 660.84

CH 3 26-Deoxycimicifugoside HPLC-DAD 5 mg 495 H3C O O O CH3 7,8-Didehydro-27-deoxyactein with UV-Spectrum CH3 common impurity of 27-Deoxyactein, 1 13 10 mg 935 O O H-NMR, C-NMR H but with a different chromophore - (with Interpretation), CH3 O from Cimicifuga racemosa O H MS, hr-MS, OH H3C CH3 OH Melting point OH Art. 3507.99 >99.0 %

[214146-75-5] C37H54O10 Mr 658.82

Dhurrin 5 mg 165 CN HPLC-DAD HO (S)-4-Hydroxymandelonitrile-β-D-glucoside with UV-Spectrum O O from Sorghum bicolor 10 mg 270 OH OH OH Art. 7001.98 >98.0 % OH [499-20-7] C14H17NO7 Mr 311.29

(+)-Dihydroquercetin see (+)-Taxifolin

OH Echimidine 5 mg 205 H C CH HPLC-DAD CH O 3 3 3 7-O-Angelyl-9-O-echimidinylretronecine with UV-Spectrum O CH3 10 mg 360 O H from Echium plantagineum OH O OH CH3 N Art. 6278.95 >95.0 % [520-68-3] C20H31NO7 Mr 397.46

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

OH H C CH CH O 3 3 Echimidine N-oxide 5 mg 205 3 HPLC-DAD O CH3 7-O-Angelyl-9-O-echimidinylretronecine N-oxide with UV-Spectrum O H OH O OH 10 mg 360 CH3 from Echium plantagineum + N O- Art. 6279.97 >97.0 % [41093-89-4] C20H31NO8 Mr 413.46

OH Echinacoside 10 mg 128 O HO HPLC-DAD HO O O OH from Echinacea pallida with UV-Spectrum HO O O 20 mg 235 O O OH HO OH H3C O Art. 6104.98 >98.0 % HO OH HO HO [82854-37-3] C35H46O20 Mr 786.70

 Echinatine sulfate 5 mg 190 HPLC-DAD H3C CH3 from Cynoglossum officinale with UV-Spectrum O CH3 10 mg 350 HO H OH O OH x 0.5 H2SO4 Art 6326.97 >97.0 %

N [480-83-1] C15H25NO5 x 0.5 H2SO4 Mr 348.40

Echinatine N-oxide 5 mg 190 H3C CH3 HPLC-DAD Cynoglossin N-oxide with UV-Spectrum O CH3 10 mg 350 HO from Cynoglossum officinale H OH O OH Art. 6296.95 >95.0 % + N [20267-93-0] - O C15H25NO6 Mr 315.36

-Elemonic acid 10 mg 246 HOOC CH3 HPLC-DAD H C from Boswellia serrata 3 CH with UV-Spectrum H 3 20 mg 452 H3C Art. 5157.98 >98.0 %

CH3 [28282-25-9] O H C30H46O3 Mr 454.70 H3C CH3

 Elenolic acid 2-O-glucoside 20 mg 175 HPLC-DAD O OCH3 Oleoside 11-methylester with UV-Spectrum 50 mg 360 HO from Olea europaea

O O Art. 2131.98 >98.0 % [60539-23-3] OGlu C17H24O11 Mr 404.38

CH Eleutheroside B 5 mg 125 3 HPLC-DAD O OH Syringin, Syringoside with UV-Spectrum 10 mg 200 O O from Syringa vulgaris HO O CH HO OH 3 Art. 3203.99 >99.0 % 20 mg 340 OH [118-34-3] C17H24O9 Mr 372.36

OCH Eleutheroside E 5 mg 134 3 HPLC-DAD O-Glucosyl Syringaresinol-4‘,4‘-O-bis--D-glucoside with UV-Spectrum O 10 mg 226 OCH3 from Eleutherococcus H H

H3CO O Art. 3202.96 >96.0 % 20 mg 382 Glucosyl-O [39432-56-9] OCH3 C34H46O18 Mr 742.71

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 OHO OH Emodin HPLC-DAD 20 mg 111 Frangula-Emodin, Rheum-Emodin, Archin with UV-Spectrum from Rhamnus frangula 50 mg 200

H3C OH O Art. 3266.99 >99.0 % [518-82-1] C15H10O5 Mr 270.23

 Englerin A 10 mg 256 HPLC-DAD from Phyllanthus engleri with UV-Spectrum OH O O O O H Art. 1901.96 >96.0 % O H [1094250-15-3] C26H35O6 Mr 442.56

 Englerin A „high purity“ 10 mg 343 HPLC-DAD from Phyllanthus engleri with UV-Spectrum OH O O O Art. 1901.99 O H O H [1094250-15-3] C26H35O6 Mr 442.56 HPLC >99 % at 215 nm, 254 nm, 280 nm filtered through a sterile filter 0.2 µm stored under Argon  CH Englerin B 5 mg 290 3 HPLC-DAD H3C from Phyllanthus engleri with UV-Spectrum O OH O O H Art. 1902.98 >98.0 % H C CH 3 H 3 [1094250-13-1] C24H32O4 Mr 384.51

(-)-Epicatechin HPLC-DAD 20 mg 120 OH EC with UV-Spectrum HO O from Acacia catechu 50 mg 232 OH

OH Art. 3305.99 >99.0 % OH [490-46-0] C15H14O6 Mr 290.27

 OH (-)-Epicatechin 3-gallate HPLC-DAD, TLC, 10 mg 230 HO O ECG 1H-NMR, 13C-NMR OH from Camellia sinensis - (with Interpretation), 50 mg 850 O UV, IR, MS, Melting OH C OH Art. 3307.RS >99.0 % O point [1257-08-5] OH OH C22H18O10 Mr 442.38

 (-)-Epicatechin 3-gallate HPLC-DAD 10 mg 90 OH ECG with UV-Spectrum HO O 20 mg 140 OH from Camellia sinensis O Art. 3307.99 >99.0 % OH C OH O [1257-08-5] OH C22H18O10 Mr 442.38 OH  OH (-)-Epigallocatechin HPLC-DAD, TLC, 10 mg 230 OH EGC 1H-NMR, 13C-NMR HO O 50 mg 850 OH from Camellia sinensis - (with Interpretation), UV, IR, MS, Melting OH Art. 3306.RS >99.0 % point OH [970-74-1]

C15H14O7 Mr 306.27

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

OH (-)-Epigallocatechin HPLC-DAD 10 mg 95 OH EGC with UV-Spectrum 20 mg 150 HO O from Camellia sinensis OH

OH Art. 3306.99 >99.0 % OH [970-74-1] C15H14O7 Mr 306.27

 OH OH (-)-Epigallocatechin 3-gallate HPLC-DAD, TLC, 20 mg 280 EGCG 1 13 HO O H-NMR, C-NMR OH from Camellia sinensis - (with Interpretation), 50 mg 550 O UV, IR, MS, Melting OH C OH Art. 3308.RS >99.0 % O point [989-51-5] OH C H O M 458.37 OH 22 18 11 r  OH OH (-)-Epigallocatechin 3-gallate HPLC-DAD 20 mg 90 HO O EGCG with UV-Spectrum OH from Camellia sinensis 50 mg 210 O OH C OH O Art. 3308.99 >99.0 % [989-51-5] OH OH C22H18O11 Mr 458.37

OH OH (-)-Epigallocatechin 3-gallate HPLC-DAD 100 mg 140 HO O EGCG with UV-Spectrum OH from Camellia sinensis O OH C OH O Art. 3308.96 >96.0 % [989-51-5] OH OH C22H18O11 Mr 458.37

 Epiprogoitrin HPLC-DAD 10 mg 140 OH (2S)-2-Hydroxybut-3-enylglucosinolate K-salt with UV-Spectrum O 20 mg 255 HOH2C O S NOSO K from Crambe abyssinica HO OH O HO Art. 3423.97 >97.0 % [21087-74-1] or [19237-18-4] (free acid) C11H18KNO10S2 Mr 427.48

 O CH3 (Z)-Erucifolin 5 mg 165 O HPLC-DAD from Senecio jacobea with UV-Spectrum HO O 10 mg 300 O O H Art. 6218.97 >97.0 % [40158-95-0] 20 mg 550 C18H23NO6 Mr 349.38 N

 O CH3 (Z)-Erucifolin N-oxide 5 mg 165 O HPLC-DAD HO from Senecio jacobea with UV-Spectrum O 10 mg 300 O O H Art. 6221.97 >97.0 % [123864-94-8] N C18H23NO7 Mr 365.38 O

 Eupatorin 20 mg 140 HPLC-DAD OCH3 3‘,5-Dihydroxy-4‘,6,7-trimethoxyflavone with UV-Spectrum CH3O O OH from Orthosiphon stamineus

CH3O Art. 3283.99 >99.0 % OH O [855-96-9]

C18H16O7 Mr 344.32

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 HO OH Europine hydrochloride 10 mg 210 HPLC-DAD O from Heliotropium with UV-Spectrum H 20 mg 380 O OCH3 HO H Art. 6214.97 >97.0 % [570-19-4] (free base) Cl N C16H28ClNO6 Mr 365.84 H

HO OH Europine N-oxide 10 mg 210 HPLC-DAD O from Heliotropium with UV-Spectrum H 20 mg 380 O OCH3 HO H Art. 6215.97 >97.0 % [65582-53-8] N C16H27NO7 Mr 345.39 O

Frangulin 100 mg 155 OHO OH HPLC-DAD Mixture of A and B approx. 1:4 with UV-Spectrum from Rhamnus frangula

H3C OR Art. 3270.97 >97.0 % O [60529-33-1] R = rhamnosyl or R = apiosyl

 Frangulin A HPLC-DAD 10 mg 100 OHO OH Emodin rhamnoside, Rhamnoxanthin with UV-Spectrum from Rhamnus frangula 20 mg 175

H3C O-Rha Art. 3268.98 >98.0 % O [521-62-0] C21H20O9 Mr 416.38

 Frangulin B HPLC-DAD 10 mg 130 OHO OH 6-O-(Apiofuranosyl)-1,6,8-trihydroxy-3-methyl- with UV-Spectrum anthraquinone 20 mg 240 from Rhamnus frangula H3C O-Api O Art. 3269.98 >98.0 % [14101-04-3] C20H18O9 Mr 402.36

 OH (-)-Gallocatechin 10 mg 140 HPLC-DAD

OH Gallocatechol, GC with UV-Spectrum 20 mg 220 HO O from Camellia sinensis OH OH Art. 3309.99 >99.0 % 50 mg 440 OH [3371-27-5] C15H14O7 Mr 306.27

 [6]-Gingerol 10 mg 135 HPLC-DAD O OH from Zingiber officinale with UV-Spectrum H3CO 20 mg 260 Art. 4301.98 >98.0 % HO [23513-14-6] C17H26O4 Mr 294.39

 O OH [8]-Gingerol 10 mg 150 HPLC-DAD H3CO from Zingiber officinale with UV-Spectrum 20 mg 283 HO Art. 4302.98 >98.0 % [23513-08-8] C19H30O4 Mr 322.44

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

O OH [10]-Gingerol 10 mg 152 HPLC-DAD H3CO from Zingiber officinale with UV-Spektrum 20 mg 288 HO Art. 4303.96 >96.0 % [23513-15-7] CH3 C21H34O4 Mr 350.50

 Ginkgolide A 10 mg 100 HPLC-DAD O O O from Ginkgo biloba with UV-Spectrum O HO 20 mg 170 H3C OH Art. 4251.98 >98.0 % O CH3 [15291-75-5] O CH O H C 3 H 3 C20H24O9 Mr 408.41

 Ginkgolide B 10 mg 110 O HPLC-DAD O O O 1-Hydroxyginkgolide A with UV-Spectrum HO H3C from Ginkgo biloba 20 mg 200 OH O CH3 O CH3 Art. 4250.99 >99.0 % O H OH CH3 [15291-77-7] C20H24O10 Mr 424.40

 Ginkgolide C 10 mg 126 HPLC-DAD O O O 1,7-Dihydroxyginkgolide A with UV-Spectrum O HO 20 mg 210 H3C from Ginkgo biloba OH O CH3 Art. 4252.97 >97.0 % O CH O H CH 3 OH OH 3 [15291-76-6] C20H24O11 Mr 440.40

 COOH Ginkgolic acids RN 5 mg 162 HPLC-DAD R OH from Ginkgo biloba with UV-Spectrum 10 mg 230 Art. 4110.90 >90.0 % [ - ] 20 mg 430

C20H32O3 / C22H34O3 / C24H38O3 R = C13H27 , C15H29 , C17H33 Mr 320.5 / 346.5 / 374.6

 H3C Glucoalyssin 5 mg 220 HPLC-DAD S O 5-(Methylsufinyl)pentylglucosinolate K-salt with UV-Spectrum from Alyssum argenteum

O Art. 3428.95 >95.0 %

HOCH - + 2 O S N O S O K HO [499-37-6] (free acid) OH HO O C13H24KNO10S3 Mr 489.63

O Glucoarabin HPLC-DAD 10 mg 160 S 9-(Methylsufinyl)nonylglucosinolate K-salt H3C with UV-Spectrum 300 from Camelina sativa O

HOCH - + 2 O S N O S O K HO Art. 3430.97 >97.0 % OH HO O [67920-64-3] (free acid) C17H32KNO10S3 Mr 545.73

 Glucobarbarin 10 mg 120 HPLC-DAD 2(S)-Hydroxy-2-phenylethylglucosinolate K-salt with UV-Spectrum S OH from Barbara variegata H O - + HOCH2 O S N O S O K HO OH Art. 3426.97 >97.0 % HO O [21087-78-5] (salt) C15H20KNO10S2 Mr 477.55

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 Glucoberteroin 5 mg 130 HPLC-DAD S 5-Methylthiopentylglucosinolate K-salt with UV-Spectrum from Berteroa incana 10 mg 215

O Art. 3412.97 >97.0 % HOH2C O S NOSO K HO OH O [245550-65-6] or [29611-01-6] (free acid) HO C13H24KNO9S3 Mr 473.64

 Glucobrassicanapin 10 mg 160 HPLC-DAD 4-Pentenylglucosinolate K-salt with UV-Spectrum 20 mg 295 O from Brassica napus

HOH2C O S NOSO HO OH O HO Art. 3419.98 >98.0 % [245550-58-7] or [19041-10-2] (free acid) C12H20KNO9S2 Mr 443.52

 Glucobrassicin 10 mg 165 HPLC-DAD N 3-Indolylmethylglucosinolate K-salt with UV-Spectrum from Brassica oleracea 20 mg 295 O HOH2C O S NOSO K HO OH Art. 3407.97 >97.0 % O HO [143231-38-3] or [4356-52-9] (free acid) C16H19KN2O9S2 Mr 486.56

H3C Glucocamelinin 10 mg 198 S HPLC-DAD O 10-(Methylsufinyl)decylglucosinolate K-salt with UV-Spectrum O from Camelina sativa HOCH - + 2 O S N O S O K HO OH HO O Art. 3431.96 >96.0 % [67884-10-0] (free acid) C18H34KNO10S3 Mr 559.76

Glucocapparin HPLC-DAD 10 mg 182

CH3 O Methylglucosinolate K-salt with UV-Spectrum

HOCH - + 2 O S N O S O K from Cleome spinosa HO OH HO O Art. 3436.98 >98.0 % [15592-33-3] or [497-77-8] (free acid) C8H14KNO9S2 Mr 371.42

 H3C Glucocheirolin HPLC-DAD 10 mg 138 O S 3-(Methylsulfonyl)propylglucosinolate K-salt O with UV-Spectrum from Cheiranthus cheiri O HOCH - 2 O S N O S O K HO Art. 3429.97 >97.0 % OH HO O [15592-36-6] (free acid)

C11H20KNO11S3 Mr 477.57

 Glucoerucin 10 mg 150 S HPLC-DAD 4-Methylthiobutylglucosinolate K-salt with UV-Spectrum from Eruca sativa 20 mg 289

O

HOH2C O S NOSO K Art. 3411.97 >97.0 % HO OH O HO [15592-37-7] or [21973-56-8] (free acid) C12H22KNO9S3 Mr 459.61

Glucohesperin HPLC-DAD 5 mg 240 H3C S 6-Methylsulfinylhexylglucosinolate K-salt with UV-Spectrum O from Hesperis matronalis 10 mg 415 O HOCH - + 2 O S N O S O K HO Art. 3439.95 >95.0 % OH HO O [33049-17-1] (free acid) C14H26KNO10S3 Mr 503.68

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

Glucohirsutin HPLC-DAD 5 mg 240 H3C S 8-(Methylsufinyl)octylglucosinolate K-salt with UV-Spectrum O from Nasturtium officinale 10 mg 414 O

HOCH - + 2 O S N O S O K Art. 3438.97 >97.0 % HO OH HO O [21973-60-4] (free acid) C16H30KNO10S3 Mr 531.70

 Glucoiberin 10 mg 128 HPLC-DAD S O 3-(Methylsulfinyl)propyglucosinolate K-salt with UV-Spectrum from Iberis amara 20 mg 215 O

HOH2C O S NOSO K HO OH 50 mg 435 O Art. 3413.99 >99.0 % HO [15592-34-4] or [554-88-1] (free acid) C11H20KNO10S3 Mr 461.56

Glucolimnanthin HPLC-DAD 10 mg 190 m-Methoxyglucotropaeolin with UV-Spectrum

H3CO from Limnanthes douglasii O

HOCH - + 2 O S N O S O K HO OH Art. 3440.97 >97.0 % HO O [111810-95-8] C15H20KNO10S2 Mr 477.55

H3C O HO Glucomoringin 10 mg 183 HO HPLC-DAD OH O 4-(α-Rhamnosyloxy)benzylglucosinolate K-salt with UV-Spectrum from Moringa oleifera

O

HOCH - + 2 O S N O S O K Art. 3437.97 >97.0 % HO OH HO O [316165-49-8] C20H28KNO14S2 Mr 609.66

 Gluconapin 10 mg 132 HPLC-DAD 3-Butenylglucosinolate K-salt with UV-Spectrum from Brassica napus 20 mg 234 O

HOH2C O S NOSO K HO OH 50 mg 465 O Art. 3417.97 >97.0 % HO [245550-57-6] or [19041-09-9] (free acid) C11H18KNO9S2 Mr 429.50

 Gluconasturtiin 10 mg 145 HPLC-DAD Phenylethylglucosinolate K-salt with UV-Spectrum from Nasturtium officinale 20 mg 247 O

HOH2C O S NOSO K HO OH O Art. 3405.97 >97.0 % HO [18425-76-8] or [499-30-9] (free acid) C15H20KNO9S2 Mr 461.54

 O S Glucoraphanin 10 mg 138 HPLC-DAD 3-(methylsufinyl)butyl-glucosinolate K-salt with UV-Spectrum 20 mg 232 O from Brassica oleracea

HOH2C O S NOSO K HO OH O Art. 3421.97 >97.0 % HO [21414-41-5] (free acid) C12H22KNO10S3 Mr 475.66

CH3 Glucoraphasatin E/Z-mixture 10 mg 200 S HPLC-DAD from Raphanus sativus with UV-Spectrum O

HOCH - + Art. 3426.97 >97.0 % 2 O S N O S O K HO OH HO O [245550-64-5] or [28463-23-2] (free acid) C12H20KNO9S3 Mr 457.58

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 O CH3 Glucoraphenin 10 mg 120 S HPLC-DAD 4-(Methylsufinyl)-3-butenylglucosinolate K-salt with UV-Spectrum 20 mg 195 O from Raphanus sativus

HOCH - + 2 O S N O SO K HO OH HO O Art. 3425.97 >97.0 % [108844-81-1] or [28463-24-3] (free acid C12H20KNO10S3 Mr 473.58

 Glucotropaeolin 20 mg 125 HPLC-DAD Benzylglucosinolate K-salt with UV-Spectrum 50 mg 252 O from Tropaeolum majus

HOH2C O S NOSO K HO OH O HO Art. 3403.99 >99.0 % [5115-71-9] or [499-26-3] (freie Säure)) C14H18KNO9S2 Mr 447.52

HO Hamamelitannin 20 mg 138 HO HPLC-DAD

O HO from Hamamelis virginiana with UV-Spectrum O O 50 mg 240 O OH OH O Art. 3315.99 >99.0 % OH HO OH [469-32-9] OH C20H20O14 Mr 484.37

HO HO Hamamelitannin HPLC-DAD 50 mg 145

O from Hamamelis virginiana HO with UV-Spectrum O O 100 mg 235 O OH OH O Art. 3315.96 >96.0 % OH HO OH [469-32-9] OH C20H20O14 Mr 484.37

 OH Harpagide 10 mg 130 HPLC-DAD OH from Harpagophytum procumbens with UV-Spectrum 20 mg 245 O Art. 2120.99 >99.0 % H HO CH 3 O-Glu [6926-08-5] C15H24O10 Mr 364.34

 Harpagoside 20 mg 295 HPLC-DAD, TLC, OH OH 8-O-Cinnamoylharpagide 1H-NMR, 13C-NMR from Harpagophytum procumbens - (with Interpretation), 50 mg 570 O O H UV, IR, MS, Melting CH3 O-Glu Art. 2121.RS >99.0 % O point [19210-12-9] C24H30O11 Mr 494.48

 Harpagoside 10 mg 95 HPLC-DAD OH OH 8-O-Cinnamoylharpagide with UV-Spectrum from Harpagophytum procumbens 20 mg 140 O O H CH3 O-Glu Art. 2121.99 >99.0 % 50 mg 280 O [19210-12-9] C24H30O11 Mr 494.48

 CH3 CH3 Hederacoside C 20 mg 220 HPLC-DAD, TLC, Hederasaponin C 1H-NMR, 13C-NMR 2 50 mg 395 CH3 CH3 H COOR from Hedera helix - (with Interpretation), CH3 UV, IR, MS, Melting R1O H Art. 5133.RS >99.0 % HO point CH3 [14216-03-6] R1 = Rha-Ara R2 = -Glu-Glu-Rha C59H96O26 Mr 1221.39

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 CH3 CH3 Hederacoside C 20 mg 112 HPLC-DAD Hederasaponin C with UV-Spectrum 2 50 mg 240 CH3 CH3 H COOR from Hedera helix

CH3

R1O 100 mg 445 H Art. 5133.99 >99.0 % HO CH3 [14216-03-6] R1 = Rha-Ara R2 = -Glu-Glu-Rha C59H96O26 Mr 1221.39

 CH3 CH3 Hederacoside C 50 mg 125 HPLC-DAD Hederasaponin C with UV-Spectrum 2 100 mg 210 CH3 CH3 H COOR from Hedera helix

CH3

R1O H Art. 5133.95 >95.0 % HO CH3 [14216-03-6] R1 = Rha-Ara R2 = -Glu-Glu-Rha C59H96O26 Mr 1221.39

 CH3 CH3 Hederagenin 20 mg 115 HPLC-DAD from Hedera helix with UV-Spectrum 50 mg 230 CH3 CH3 H COOH Art. 5135.98 >98.0 % CH3 HO [465-99-6] H HO CH C H O M 472.73 3 30 48 4 r

 CH3 CH3 Hederagenin 100 mg 175 HPLC-DAD from Hedera helix with UV-Spectrum CH3 CH3 H COOH Art. 5135.90 >90.0 % CH3 HO [465-99-6] H HO CH3 C30H48O4 Mr 472.73

CH3 CH3 -Hederin 10 mg 110 HPLC-DAD from Hedera helix with UV-Spectrum 20 mg 170 CH3 CH3 H COOH Art. 5136.99 >99.0 % CH3 [27013-91-8] 50 mg 350 Rha-Ara-O H HO CH3 C41H66O12 Mr 750.97

OH Heliosupine 5 mg 183 HPLC-DAD H C CH CH O 3 3 3 Cynoglossophine with UV-Spectrum O CH3 10 mg 335 O H from Cynoglossum officinale OH O OH CH3 N Art. 6297.95 >95.0 % [32728-78-2] C20H31NO7 Mr 397.46

OH Heliosupine N-oxide 5 mg 183 HPLC-DAD H C CH CH O 3 3 3 Cynoglossophine N-oxide with UV-Spectrum O CH3 10 mg 335 O H from Cynoglossum officinale OH O OH CH3 + N Art. 6298.95 >95.0 % O- [31701-88-9] C20H31NO8 Mr 413.46

OH Heliotridine HPLC-DAD 5 mg 250 HO H from Heliotropium europaeum with UV-Spectrum 10 mg 470 Art. 6286.97 >97.0 % [520-63-8] N C H NO M 155.19 8 13 2 r

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

OH Heliotridine N-oxide HPLC-DAD 5 mg 270 HO H from Heliotropium europaeum with UV-Spectrum 10 mg 520 Art. 6287.97 >97.0 % + N [ - ] - C8H13NO3 Mr 171.19 O

 Heliotrine 10 mg 112 OH HPLC-DAD O from Heliotropium with UV-Spectrum 20 mg 168 H O OCH3 HO Art. 6212.98 >98.0 % H [303-33-3] C16H27NO5 Mr 313.39 N

OH Heliotrine N-oxide 10 mg 143 HPLC-DAD O from Heliotropium with UV-Spectrum H 20 mg 220 O OCH3 HO H Art. 6213.97 >97.0 % [6209-65-0] N C16H27NO6 Mr 329.39 O

 Hesperetin HPLC-DAD 20 mg 110 OCH3 Cyanidanon 4‘-methylether with UV-Spectrum HO O 50 mg 215 OH synthetic Art. 3320.98 >98.0 % OH O [41001-90-5] C16H14O6 Mr 302.28

 Hesperidin 20 mg 115 OCH3 HPLC-DAD Hesperetin 7-rutinoside, Cirantin Rha-Glc-O O with UV-Spectrum OH from Citrus sinensis 50 mg 230

OH Art. 3321.98 >98.0 % O [520-26-3] C28H34O15 Mr 610.57

 OH Homoorientin 5 mg 108 HPLC-DAD 6-C-Glucoluteolin, Isoorientin HO O with UV-Spectrum OH from Adonis vernalis 10 mg 160 Glu Art. 3277.99 >99.0 % 20 mg 290 OH O [4261-42-1] C21H20O11 Mr 448.38

 COOH O 7-Hydroxyaristolochic acid I HPLC-DAD 10 mg 328 NO 7-Hydroxyaristolochic acid A with UV-Spectrum O 2 20 mg 594 from Aristolochia clematitis Art. 4616.98 >98.0 %

OCH3 [79185-75-4] OH C17H11NO8 Mr 357.27

 N 4-Hydroxyglucobrassicin HPLC-DAD 5 mg 250 4-Hydroxy-3-indolylmethylglucosinolate K-salt with UV-Spectrum OH O from Brassica oleracea N O S O- K+ HOCH2 O S HO OH O Art. 3427.95 >95.0 % HO [83327-20-2] (free acid) C16H19KN2O10S2 Mr 502.56

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

13-Hydroxylupanine HPLC-DAD 5 mg 250 H 13α-Hydroxy-2-sparteinone N with UV-Spectrum from Lupinus angustifolius N OH H Art. 6321.95 >95.0 % O [15358-48-2] C15H24N2O2 Mr 264.37

H3C HO CH2OH 18-Hydroxyspartioidine HPLC-DAD 5 mg 245 O (15E)-Riddelliine with UV-Spectrum from Senecio riddellii CH2 O O O H Art. 6318.95 >95.0 % [-] N C18H23NO6 Mr 349.38

 Hydroxytyrosol HPLC-DAD, TLC, 25 mg 240 HO CH2 CH2OH 2-(3,4-Dihydroxyphenyl)ethanol 1H-NMR, 13C-NMR from Olea europaea - (with Interpretation), HO UV, IR, MS Art. 4440.RS >98.0 %

[10597-60-1] C8H10O3 Mr 154.17

 Hydroxytyrosol HPLC-DAD 25 mg 120 2-(3,4-Dihydroxyphenyl)ethanol with UV-Spectrum HO CH2 CH2OH from Olea europaea 50 mg 195

HO Art. 4440.98 >98.0 % [10597-60-1] C8H10O3 Mr 154.17

 OH CH3 Hydroxyvalerenic acid 25 mg 276 H HPLC-DAD (2 from Valeriana officinalis methods), TLC (2 methods), 50 mg 445 Art. 4401.RS >99.0 % 1H-NMR, 13C-NMR CH3 [1619-16-5] 100 mg 745 CH3 - (with Interpretation), C15H22O3 Mr 250.34 UV, IR, MS, Elemental COOH analysis, Melting point

 OH CH3 Hydroxyvalerenic acid 10 mg 105 H HPLC-DAD from Valeriana officinalis with UV-Spectrum 25 mg 189 Art. 4401.99 >99.0 % CH [1619-16-5] 50 mg 325 3 CH3 C15H22O3 Mr 250.34 COOH

 Hyperforin / Adhyperforin- HPLC-DAD 5 mg 170 H N 2 Dicyclohexylammonium salt (4:1) with UV-Spectrum 10 mg 315 O natural mixture from Hypericum perforatum O Art. 4213.95 >95.0 % O O [238074-03-8] C35H51O4 x C12H24N Mr 718.11

 OH O OH Hypericin 10 mg 395 HPLC-DAD, TLC, from Hypericum perforatum 1H-NMR, 13C-NMR HO CH3 - (with HO CH 3 Art. 3720.RS >98.0 % Interpretation), [548-04-9] UV, IR, MS, hr-MS, C H O M 504.45 OHO OH 30 16 8 r Melting point

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 OH O OH Hypericin 5 mg 170 HPLC-DAD from Hypericum perforatum with UV-Spectrum HO CH3 10 mg 290 HO CH3 Art. 3720.98 >98.0 % [548-04-9] 20 mg 510

OHO OH C30H16O8 Mr 504.45

 OH O OH Hypericin Sodium salt 5 mg 195 HPLC-DAD Na from Hypericum perforatum with UV-Spectrum O CH3 10 mg 317 HO CH3 Art. 3721.98 >98.0 % [ - ] 20 mg 530 C30H15O8Na Mr 526.43 OHO OH

 Hyperoside 20 mg 195 HPLC-DAD (2 OH Hyperin, Quercetin 3-galactoside methods), TLC, HO O 1 13 50 mg 360 OH from Hypericum perforatum H-NMR, C-NMR - (with Interpretation), 100 mg 580 O-Gal Art. 3252.RS >99.0 % UV, IR, MS, Melting OH O [482-36-0] point C21H20O12 Mr 464.38

 Hyperoside 20 mg 126 HPLC-DAD OH Hyperin, Quercetin 3-galactoside with UV-Spectrum HO O from Hypericum perforatum 50 mg 257 OH O-Gal Art. 3252.99 >99.0 % 100 mg 429 OH O [482-36-0] C21H20O12 Mr 464.38

 Hyperoside 100 mg 170 OH HPLC-DAD Hyperin, Quercetin 3-galactoside with UV-Spectrum HO O OH from Hypericum perforatum

O-Gal Art. 3252.97 >97.0 % OH O [482-36-0] C21H20O12 Mr 464.38

 H3C CH3 Icariin 10 mg 122 HPLC-DAD OCH Ieariline with UV-Spectrum glu 3 from Epimedium brevicornum 20 mg 230 O O

O Art. 3259.99 >99.0 % OH O rha [489-32-7] C33H40O15 Mr 676.65

 OH Indicine hydrochloride 10 mg 188 HPLC-DAD O from Heliotropium indicum with UV-Spectrum 20 mg 333 O H OH HO H Art. 6216.97 >97.0 % [1195140-94-3] Cl N C15H26ClNO5 Mr 335.83 H

 OH Indicine N-oxide 10 mg 208 HPLC-DAD O from Heliotropium with UV-Spectrum O H OH 20 mg 374 HO H Art. 6217.96 >96.0 % [41708-76-3] N C15H25NO6 Mr 315.36 O

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

CH 3 HO CH3 Integerrimine HPLC-DAD 5 mg 235 O Intergerrimine, Squalidin(e) with UV-Spectrum from Senecio vulgaris 10 mg 420 CH3 O O O H Art. 6283.97 >97.0 % [480-79-5] N C18H25NO5 Mr 335.39

CH 3 HO CH3 Integerrimine N-oxide HPLC-DAD 5 mg 250 O Intergerrimine N-oxide, Squalidin(e) N-oxide with UV-Spectrum 10 mg 450 CH3 O from Senecio vulgaris O O H Art. 6284.95 >95.0 % + [85955-28-8] N - C H NO M 351.39 O 18 25 6 r

H3C CH3 Intermedine 5 mg 180 HPLC-DAD from Symphytum officinale with UV-Spectrum O CH 10 mg 315 HO H OH Art. 6274.95 >95.0 % O OH [10285-06-0] N C15H25NO5 Mr 299.36

H3C CH3 Intermedine N-oxide 5 mg 205 HPLC-DAD

O CH3 from Symphytum officinale with UV-Spectrum HO H 10 mg 358 OH O OH Art. 6275.95 >95.0 % + N [95462-14-9] - O C15H25NO6 Mr 315.37

 Isoacteoside 20 mg 186 HPLC-DAD O HO Isoverbascoside with UV-Spectrum O from Harpagophytum procumbens 50 mg 379 HO HO O O O OH OH H3C O HO OH Art. 6102.99 >99.0 % HO HO [61303-13-7] C29H36O15 Mr 624.59

 Isoorientin see Homoorientin

 Isoquercitrin 20 mg 225 HPLC-DAD (2 OH Quercetin 3-glucoside, Hirsutrin, methods), TLC, HO O 1 13 50 mg 410 OH from Sambucus nigra H-NMR, C-NMR - (with Interpretation), O-Glu 100 mg 665 Art. 3254.RS >99.0 % UV, IR, MS, Melting OH O [482-35-9] point C21H20O12 Mr 464.38

 Isoquercitrin 20 mg 125 HPLC-DAD OH Quercetin 3-glucoside, Hirsutrin, Isoquercetin with UV-Spectrum HO O 50 mg 245 OH from Tiliae officinalis O-Glu Art. 3254.99 >99.0 % 100 mg 440 OH O [482-35-9]

C21H20O12 Mr 464.38

 Isoquercitrin 50 mg 185 HPLC-DAD OH Quercetin 3-glucoside, Hirsutrin, Isoquercetin with UV-Spectrum HO O 100 mg 335 OH from Tiliae officinalis

O-Glu Art. 3254.97 >97.0 % OH O [482-35-9] C21H20O12 Mr 464.38

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 Isorhamnetin 10 mg 112 HPLC-DAD OCH 3 4'-O-Methylquercetin with UV-Spectrum HO O 20 mg 193 OH from Calendula officinalis

OH Art. 3251.98 >98.0 % OH O [480-19-3] C16H12O7 Mr 316.27

 Isoverbascoside see Isoacteoside

 OH Isovitexin 5 mg 200 HPLC-DAD, TLC, HO O 6-Glucosylapigenin 1H-NMR, 13C-NMR from Passiflora incarnata - (with 10 mg 315 Glu Interpretation), OH O Art. 3230.RS >99.0 % UV, IR, MS, Melting [38953-85-4] point C21H20O10 Mr 432.38

 OH Isovitexin 5 mg 124 HPLC-DAD HO O 6-Glucosylapigenin with UV-Spectrum from Passiflora incarnata 10 mg 185 Glu OH O Art. 3230.99 >99.0 % [38953-85-4] C21H20O10 Mr 432.38

 Isoxanthohumol 10 mg 135 HPLC-DAD OH from Humulus lupulus with UV-Spectrum 20 mg 198 HO O Art. 3325.99 >99.0 % [70872-29-6] 50 mg 395 C21H22O5 Mr 354.40 OCH3 O

O HO CH3  O Jacobine 5 mg 175 HPLC-DAD from Senecio jacobea with UV-Spectrum CH O O O 3 10 mg 310 H Art. 6219.98 >98.0 % [6870-67-3] N C18H25NO6 Mr 351.39

O HO CH3  O Jacobine N-oxide 5 mg 187 HPLC-DAD from Senecio jacobea with UV-Spectrum CH3 O 10 mg 330 O O H Art. 6222.96 >96.0 % [38710-25-7] N C18H25NO7 Mr 367.39 O

CH  3 HO CH3 OH Jacoline 5 mg 235 HPLC-DAD O HO from Senecio jacobea with UV-Spectrum 10 mg 410 CH3 O O O H Art. 6291.97 >97.0 % [480-76-2] C18H27NO7 Mr 369.41 N

CH3 HO CH  OH 3 Jacoline N-oxide 5 mg 255 HPLC-DAD O HO from Senecio jacobea with UV-Spectrum 10 mg 460 CH3 O O O H Art. 6292.97 >97.0 % [1148039-73-9 ] + C H NO M 385.41 N 18 27 8 r - O

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

CH 3 HO CH3 Jaconine 5 mg 290 OH HPLC-DAD O from Senecio jacobea with UV-Spectrum Cl 10 mg 540 CH3 O O O H Art. 6293.95 >95.0 % [480-75-1] N C18H26ClNO6 Mr 387.86

CH  3 HO CH3 OH Jaconine N-oxide 5 mg 390 HPLC-DAD O from Senecio jacobea with UV-Spectrum Cl CH3 O O O H Art.-Nr. 6294.95 >95.0 % [1148039-75-1] + N C18H26ClNO7 Mr 403.85 - O

 Kaempferol 20 mg 220 OH HPLC-DAD, TLC, Robigenin, Trifolitin 1H-NMR, 13C-NMR HO O from Aesculus hippocastanum - (with Interpretation), 50 mg 420 UV, IR, MS, Melting OH 100 mg 700 Art. 3240.RS >99.0 % point OH O [520-18-3] C15H10O6 Mr 286.24

 Kaempferol 20 mg 110 OH HPLC-DAD Robigenin, Trifolitin with UV-Spectrum HO O from Aesculus hippocastanum 50 mg 220

OH Art. 3240.99 >99.0 % 100 mg 440 OH O [520-18-3] C15H10O6 Mr 286.24

 Kaempferol 250 mg 165 OH HPLC-DAD Robigenin, Trifolitin with UV-Spectrum HO O from Aesculus hippocastanum 500 mg 295

OH Art. 3240.97 >97.0 % OH O [520-18-3] C15H10O6 Mr 286.24

 OH Kaempferol 3-glucoside 10 mg 180 HPLC-DAD HO O with UV-Spectrum from Aesculus hippocastanum 20 mg 330 O-Glu Art. 3242.99 >99.0 % 50 mg 740 OH O [480-10-4] C21H20O11 Mr 448.38

 OH Kaempferol 3-glucoside 20 mg 175 HPLC-DAD HO O Astragalin with UV-Spectrum from Aesculus hippocastanum 50 mg 320 O-Glu Art. 3242.97 >97.0 % OH O [480-10-4] C21H20O11 Mr 448.38

 CH3 H C 11-Keto--boswellic acid 5 mg 125 3 HPLC-DAD H 3-Hydroxyurs-12-ene-11-keto-23-oic acid with UV-Spectrum O 10 mg 197 CH from Boswellia serrata H3C 3 CH3 H CH3 Art. 5152.99 >99.0 % 20 mg 346 HO H [17019-92-0] HOOC CH3 C30H46O4 Mr 470.69

 Kuromanin chloride see Cyanidin 3-glucoside chloride

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 HO Lasiocarpine 10 mg 168 OH HPLC-DAD O 7-Angelyleuropine with UV-Spectrum H 20 mg 295 O OCH3 from Heliotropium O O H Art. 6210.97 >97.0 % N [303-34-4] C21H33NO7 Mr 411.49

 HO OH Lasiocarpine N-oxide 10 mg 168 HPLC-DAD O 7-Angelyleuropine N-oxide with UV-Spectrum H 20 mg 295 O OCH3 from Heliotropium O O H Art. 6211.96 >96.0 % N [127-30-0] O C21H33NO8 Mr 427.49

Glc  CH3 O Leiocarposide 10 mg 210 O HPLC-DAD 2’-Hydroxybenzyl-3-methoxybenzoate 2',4- with UV-Spectrum O diglucoside 20 mg 366 O OH from Solidago virgaurea Glc-O Art. 2125.99 >99.0 % [71953-77-0] C27H34O16 Mr 614.56  OCH3 Linarin 10 mg 128 Glu-Rha HPLC-DAD O O Acacetin 7-rutinoside with UV-Spectrum from Linaria vulgaris

Art. 3210.98 >98.0 % OH O [480-36-4]

C28H32O14 Mr 592.57

Lucidin 3-primveroside 10 mg 220 O OH HPLC-DAD CH2OH Lucidin-3-O-beta-primveroside with UV-Spectrum O from Rubia tinctorium O O HO O O OH Art. 3708.98 >98.0 % HO OH HO OH [29706-59-0] C26H28O14 Mr 564.49

- Lupanine hydrochloride 10 mg 250 Cl HPLC-DAD H 2-Oxospartein H + with UV-Spectrum N from Lupinus angustifolius

N Art. 6351.95 >95.0 % H [1025-39-4] O C15H25ClN2O Mr 284.83

 Lutein 5 mg 136 HPLC-DAD Xanthophyll, ,-Carotene-3,3'-diol with UV-Spectrum OH from Brassica oleracea

HO Art. 4205.90 >90 % [127-40-2] C40H56O2 Mr 568.88

 OH Luteolin 20 mg 240 HPLC-DAD, TLC, OH 1 13 Digitoflavone H-NMR, C-NMR 50 mg 395 HO O from Reseda luteola - (with Interpretation), Art. 3260.RS >99.0 % UV, IR, MS, Melting OH O [491-70-3] point C15H10O6 Mr 286.23

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 OH Luteolin 20 mg 125 HPLC-DAD OH Digitoflavone with UV-Spectrum 50 mg 255 HO O from Reseda luteola

Art. 3260.99 >99.0 % 100 mg 480 OH O [491-70-3] C15H10O6 Mr 286.23

 OH Luteolin 7-glucoside 20 mg 240 HPLC-DAD (2 OH Glucoluteolin methods) 50 mg 395 GluO O from Reseda luteola TLC, 1H-NMR, 13C- NMR Art. 3262.RS >99.0 % - (with OH O [5373-11-5] Interpretation), C21H20O11 Mr 448.38 UV, IR, MS, Melting point  OH Luteolin 7-glucoside 20 mg 120 HPLC-DAD OH  Glucoluteolin with UV-Spectrum 50 mg 250 GluO O from Reseda luteola  Art. 3262.99 >99.0 % 100 mg 470 OH O [5373-11-5]

C21H20O11 Mr 448.38

 Lycopene 5 mg 140 HPLC-DAD ,-Carotene, (all-trans)-Lycopene with UV-Spectrum from Solanum lycopersicum Art. 4207.90 >90 % [502-65-8] C40H56 Mr 536.88

Lycopsamine 5 mg 178 H3C CH3 HPLC-DAD from Symphytum officinale with UV-Spectrum O CH3 10 mg 315 HO H OH Art. 6270.95 >95.0 % O OH [10285-07-1] N C15H25NO5 Mr 299.36

H C CH Lycopsamine N-oxide 5 mg 205 3 3 HPLC-DAD from Symphytum officinale with UV-Spectrum O CH 3 10 mg 358 HO H OH O OH Art.-Nr. 6271.95 >95.0 % [95462-15-0] N+ C15H25NO6 Mr 315.36 O-

 (-)-Maackiain 10 mg 150 HPLC-DAD HO O Demethylpterocarpin, Inermin with UV-Spectrum H 20 mg 260 O from Baptisia tinctoria H O O Art. 3226.98 >98.0 % [2035-15-6] C16H12O5 Mr 284.27

H3CO Malvidin chloride HPLC-DAD 10 mg 129 OH Cl- from Malva silvestris with UV-Spectrum + HO O Art. 5008.97 >97.0 % OCH3 [643-84-5] OH C17H15ClO7 Mr 366.75 OH

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

OCH3 Malvidin 3-galactoside chloride HPLC-DAD 5 mg 136 OH , Arthanitin chloride Cl with UV-Spectrum 10 mg 235 HO O from Vaccinium myrtillus OCH3 Art. 5011.95 >95.0 % OGlu [30113-37-2] OH C23H25ClO12 Mr 528.89

Malvidin 3-glucoside chloride see Oenin chloride

OCH3 Malvin chloride HPLC-DAD 10 mg 105 OH Malvidin 3,5-diglucoside chloride with UV-Spectrum Cl from Malva silvestris 20 mg 170 HO O OCH 3 Art. 5005.97 >97.0 % 50 mg 350 OGlu [16727-30-3]

OGlu C29H35ClO17 Mr 691.04

Malvin chloride 100 mg 165 OCH3 HPLC-DAD Malvidin 3,5-diglucoside chloride OH with UV-Spectrum Cl from Malva silvestris HO O OCH3 Art. 5005.90 >90.0 % OGlu [16727-30-3] OGlu C29H35ClO17 Mr 691.04

 Manassantin A 10 mg 215 O HPLC-DAD HO OH O from Saururus chinensis with UV-Spectrum H3CO OCH3 20 mg 370

CH3O OCH3 Art. 3101.98 >98.0 % OCH3 OCH3 [88497-87-4] C42H52O11 Mr 732.34

 Manassantin B HPLC-DAD 10 mg 185 O HO OH from Saururus chinensis with UV-Spectrum O 20 mg 323 H3CO OCH3 Art. 3103.98 >98.0 % O OCH3 O OCH3 [88497-88-5] C41H48O11 Mr 716.30

Cl CH3 OH Merenskine 5 mg 153 OH CH3 HPLC-DAD O Chlordeoxysceleratine with UV-Spectrum from Senecio retrorsus 10 mg 285 CH3 O O O H Art. 6223.97 >97.0 % [96657-94-2] N C18H26ClNO6 Mr 387.85

Cl  CH3 OH OH CH3 Merenskine N-oxide HPLC-DAD 5 mg 153 O Chlordeoxysceleratinyl-N-oxide with UV-Spectrum from Senecio retrorsus 10 mg 285 CH3 O O O H Art. 6225.97 >97.0 % [96657-95-3] N C18H26ClNO7 Mr 403.85 O

 CH3 OH O CH3 Merepoxine HPLC-DAD 5 mg 173 O from Senecio retrorsus with UV-Spectrum 10 mg 315 CH3 O O O Art. 6224.97 >97.0 % H [115777-94-1] C18H25NO6 Mr 351.40 N

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

CH3 OH O CH3 O Merepoxine N-oxide HPLC-DAD 5 mg 173 from Senecio retrorsus with UV-Spectrum CH3 O 10 mg 315 O O H Art. 6226.97 >97.0 % [ - ] N C H NO M 367.40 O 18 25 7 r

N 4-Methoxyglucobrassicin HPLC-DAD 5 mg 198 4-Methoxy-3-indolylmethylglucosinolate K-salt with UV-Spectrum O H3C O + N O S O- K from Brassica oleracea HOCH2 O S HO OH O HO Art. 3433.94 >94.0 % [83327-21-3] (free acid) C17H21KN2O10S2 Mr 516.59

11-(Methylsulfinyl)undecylglucosinolate 5 mg 185 O HPLC-DAD S Homoglucocamelinin K-salt H3C with UV-Spectrum from Camelina sativa 10 mg 350 O

HOCH - + 2 O S N O S O K HO OH HO O Art. 3432.97 >97.0 % [186037-18-3] C19H36KNO10S3 Mr 573.79

H3COH CH3  OH Monocrotaline 20 mg 100 H3C O HPLC-DAD from Crotalaria with UV-Spectrum O O 50 mg 180 O Art. 6227.99 >99.0 % H [315-22-0]

N C16H23NO6 Mr 325.36

H3COH CH3  OH Monocrotaline N-oxide 10 mg 205 H3C O HPLC-DAD from Crotalaria with UV-Spectrum O O 20 mg 360 O H Art. 6228.98 >98.0 % [35337-98-5] N C16H23NO7 Mr 341.36 O

 Morindin HPLC-DAD 10 mg 212 OH O from Morinda citrifolia with UV-Spectrum CH3 CH2OH O O O OH O OH OH Art. 3271.97 >97.0 % O OH HO HO [60450-21-7] C26H28O14 Mr 564.50

Multiflorine HPLC-DAD 5 mg 280 H 4-Oxo-2,3-didehydrosparteine O N with UV-Spectrum from Lupinus albus 10 mg 500 N H Art. 6324.95 >95.0 % [529-80-6] C15H22N2O Mr 246.35

OH

OH Myricitrin 20 mg 129 HPLC-DAD 3-rhamnoside, Myricitroside with UV-Spectrum HO O OH from Myrica cerifera 50 mg 258

O-Rha OH O Art. 3258.99 >99.0 % [17912-87-7] C21H20O12 Mr 464.38

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 OH Narciclasin 10 mg 215 OH HPLC-DAD Lycoricidinol with UV-Spectrum H O 20 mg 373 OH from Narcissus pseudonarcissus NH O Art. 6350.97 >97.0 % OH O [29477-83-6] C14H13NO7 Mr 307.26

 Naringenin 20 mg 112 HPLC-DAD OH Naringetol, Pelarginadon with UV-Spectrum 50 mg 223 HO O from Citrus paradisi Art. 3323.98 >98.0 % [480-41-1] OH O C15H12O5 Mr 272.26

 Naringin 20 mg 112 HPLC-DAD OH Naringenin 7-rhamnoglucoside, Aurantiin with UV-Spectrum 50 mg 223 Rha-Glc-O O from Citrus paradisi Art. 3322.99 >99.0 % OH O [10236-47-2] C27H32O14 Mr 580.54

Neoglucobrassicin HPLC-DAD 5 mg 198 O CH3 N 1-Methoxy-3-indolylmethylglucosinolate K-salt with UV-Spectrum from Brassica oleracea O N O S O- K+ HOCH2 O S HO Art. 3434.97 >97.0 % OH O HO [5187-84-8] (free acid) C17H21KN2O10S2 Mr 516.59

OCH3 Oenin chloride HPLC-DAD 10 mg 148 OH Cl Malvidin 3-glucoside chloride with UV-Spectrum HO O from Vitis vinifera 20 mg 252 OCH3

OGlu Art. 5007.97 >97.0 % OGlu [7228-78-6] C23H25ClO12 Mr 528.89

OCH3 Oenin chloride HPLC-DAD 100 mg 190 OH Cl Malvidin 3-glucoside chloride with UV-Spectrum HO O from Vitis vinifera OCH3

OGlu Art. 5007.85 >85.0 % [7228-78-6] OH C23H25ClO12 Mr 528.89

 O OCH Oleuropein 20 mg 240 3 HPLC-DAD, TLC, 1 13 HO O from Olea europaea H-NMR, C-NMR - (with Interpretation), 50 mg 395 O O HO Art. 2111.RS >98.0 % UV, IR, MS, Melting OGlu [32619-42-4] point C25H32O13 Mr 540.52

 O OCH Oleuropein 20 mg 140 3 HPLC-DAD from Olea europaea with UV-Spectrum HO O 50 mg 280 O O HO Art. 2111.98 >98.0 % OGlu [32619-42-4] C25H32O13 Mr 540.52

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 O OCH Oleuropein 500 mg 155 3 HPLC-DAD from Olea europaea with UV-Spectrum HO O 1000 mg 250 O O HO Art. 2111.90 >90.0 % OGlu [32619-42-4] C25H32O13 Mr 540.52

H3C CH3 HO  -Onocerin 10 mg 170 HPLC-DAD from Ononis spinosa with UV-Spectrum CH2 CH3 20 mg 308 Art. 4214.98 >98.0 % CH3 H2C [511-01-3]

OH C30H50O2 Mr 442.72

H3C CH3

 OH Orientin 5 mg 112 HPLC-DAD Glu 8-C-Glucoluteolin, Lutexin with UV-Spectrum HO O OH from Adonis vernalis 10 mg 169 Art. 3276.99 >99.0 % OH O [28608-75-5] C21H20O11 Mr 448.36

 Otonecin 1 mg 150 HPLC-DAD HO OH O from Senecio vulgaris with UV-Spectrum 5 mg 330 Art.-Nr. 6288.95 >95.0 % N [6887-34-9] C H NO M 185.22 CH3 9 15 3 r

 Pectolinarigenin 10 mg 170 HPLC-DAD OCH3 5,7-Dihydroxy-4‘,6-dimethoxyflavone with UV-Spectrum HO O from Linaria vulgaris 20 mg 300

H3CO Art. 3212.97 >97.0 % OH O [520-12-7] C17H14O6 Mr 314.30

 OCH Pectolinarin 10 mg 170 HPLC-DAD Glu-Rha 3 Pectolinaroside, Neolinarin with UV-Spectrum O O from Linaria vulgaris 20 mg 300

H3CO Art. 3211.98 >98.0 % OH O [28978-02-1] C29H34O15 Mr 622.58

Pelargonidin chloride 10 mg 144 HPLC-DAD - OH Cl from Pelargonium zonale with UV-Spectrum HO O+ Art. 5006.97 >97.0 % OH [134-04-3] OH C15H11O5Cl Mr 306.70

- OH Pelargonidin 3,5-diglucoside chloride 5 mg 115 Cl HPLC-DAD

+ chloride, Salvinin HO O with UV-Spectrum from Pelargonium zonale 10 mg 210 O-Glu Art. 5025.97 >97.0 % O-Glu [17334-58-6] C27H31O15Cl Mr 630.97

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

OH Cl- Pelargonidin 3-glucoside chloride 5 mg 125 HPLC-DAD HO O+ from Fragaria with UV-Spectrum 10 mg 195 Art. 5024.96 >96.0 % O-Glu [18466-51-8] OH C21H21O10Cl Mr 468.84

OH Penduletin HPLC-DAD 5 mg 160 5,4'-Dihydroxy-3,6,7-trimethoxyflavone H CO with UV-Spectrum 3 O from Vitex agnus castus 10 mg 280

OCH H3CO 3 Art. 3327.97 >97.0 % OH [569-80-2] C18H16O7 Mr 344.32

OCH3 Peonidin chloride HPLC-DAD 5 mg 125 OH Cl- from Rosa centifolia with UV-Spectrum + HO O 10 mg 235 Art. 5010.97 >97.0 %

OH [134-01-0] OH C16H13ClO6 Mr 336.73

OCH Peonidin 3,5-diglucoside chloride 5 mg 140 3 HPLC-DAD OH Cl- Paeonine with UV-Spectrum 10 mg 230 HO O+ from Rosa centifolia Art. 5026.95 >95.0 % O-Glu [132-37-6] O-Glu C28H33O16Cl Mr 661.01

OCH Peonidin 3-glucoside chloride 5 mg 150 3 HPLC-DAD - OH from Vitis vinifera with UV-Spectrum Cl 10 mg 258 + HO O Art. 5020.96 >96.0 % [6906-39-4] O-Glu C22H23O11Cl Mr 498.85 OH

OCH3 Petunidin 3-glucoside chloride 5 mg 150 HPLC-DAD OH Cl from Vitis vinifera with UV-Spectrum HO O 10 mg 265 OH Art. 5021.97 >97.0 % OGlu [6988-81-4] OH C22H23O12Cl Mr 514.85

O Picroside II 20 mg 125 HPLC-DAD

CH3O O H 6-Vanilloylcatalpol with UV-Spectrum from Picrorhiza kurrooa 50 mg 260 HO O O Art. 2104.98 >98.0 % H CH2OHO-Glu [39012-20-9] C23H28O13 Mr 512.47

 O Primin 20 mg 290 HPLC-DAD (2 H3CO 2-Methoxy-6-pentyl-p-benzoquinone methods), synthetic TLC (2 methods), 50 mg 550 1H-NMR, 13C-NMR O Art. 1001.RS >99.0 % - (with Interpretation), [15121-94-5] UV, IR, MS, Melting C12H16O3 Mr 208.26 point, Elemental analysis

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 O Primin 20 mg 190 HPLC-DAD H3CO 2-Methoxy-6-pentyl-p-benzoquinone with UV-Spectrum synthetic 50 mg 410

O Art. 1001.99 >99.0 % 100 mg 745 [15121-94-5] C12H16O3 Mr 208.26

 Primulaverin 10 mg 156 HPLC-DAD O OCH3 C from Primula veris with UV-Spectrum 20 mg 268 O-Glu-Xyl Art. 4101.99 >99.0 % [154-61-0] H3CO C20H28O13 Mr 476.43

 O OCH3 Primverin 10 mg 157 HPLC-DAD C Primeverin with UV-Spectrum O-Glu-Xyl from Primula veris 20 mg 264 Art. 4102.99 >99.0 % OCH3 [154-60-9] C20H28O13 Mr 476.43

 Progoitrin 10 mg 120 HPLC-DAD 2-Hydroxybut-3-enylglucosinlate K-salt with UV-Spectrum OH 20 mg 230 O from Brassica napus HOH2C O S NOSO K HO OH O 50 mg 470 HO Art. 3415.97 >97.0 % [21087-77-4] or [585-95-5] (free acid) C11H18KNO10S2 Mr 427.48

 Protopine 10 mg 132 O HPLC-DAD

H3C N Fumarine, Biflorine, Macleyine with UV-Spectrum O 20 mg 243 O from Chelidonium majus O Art. 6307.98 >98.0 % 50 mg 505 O [130-86-9] C20H19NO5 Mr 353.37

OHO OH Pseudohypericin 5 mg 190 HPLC-DAD from Hypericum perforatum with UV-Spectrum 10 mg 300 HO CH2OH

HO CH3 Art. 3272.97 >97.0 % [55954-61-5] 20 mg 520 C30H16O9 Mr 520.43 OH O OH

OH

HO OH  HO Punicalagin 10 mg 125 HO HPLC-DAD O O O from Punica granatum with UV-Spectrum O O 20 mg 235 OH O

HO OH O Art. 3313.97 >97.0 %

OH O OH O HO O O O [65995-63-3] O

HO OH C48H28O30 Mr 1084.72

HO OH HO OH

 OH HO OH Punicalin 10 mg 175 HO HPLC-DAD HO

O from Punica granatum with UV-Spectrum O 20 mg 325 O O O OH O Art. 3314.97 >97.0 % HO OH O [65995-64-4] HO OH OH OH HO O C34H22O22 Mr 782.53 O

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 OH Quercetin 20 mg 220 HPLC-DAD, TLC, 1 13 HO O Sophoretin, Meletin H-NMR, C-NMR OH synthetic from Rutin - (with Interpretation), 50 mg 315 OH UV, IR, MS, Melting OH O 100 mg 520 Art. 3201.RS >99.0 % point, [117-39-5] Elemental analysis C15H10O7 Mr 302.24  OH Quercetin dihydrate 20 mg 95 HPLC-DAD

HO O Sophoretin, Meletin with UV-Spectrum OH synthetic from Rutin 50 mg 175 OH OH O Art. 3201.99 >99.0 % 100 mg 300 [6151-25-3]  C15H10O7 2H2O Mr 338.27

 OH Quercitrin 10 mg 225 HPLC-DAD (2 HO O Quercetin 3-rhamnoside, Quercitroside methods) OH from Aesculus hippocastanum TLC, 1H-NMR, 13C- 20 mg 355 O-Rha NMR OH O 50 mg 685 Art. 3253.RS >99.0 % - (with Interpretation), [522-12-3] UV, IR, MS, Melting C21H20O11 Mr 448.38 point

 OH Quercitrin 10 mg 95 HPLC-DAD HO O Quercetin 3-rhamnoside, Quercitroside with UV-Spectrum OH from Aesculus hippocastanum 20 mg 160 O-Rha OH O Art. 3253.99 >99.0 % 50 mg 325 [522-12-3] C21H20O11 Mr 448.38

OH Retronecine HPLC-DAD 5 mg 180 HO H Retronecin, Senecifolinene with UV-Spectrum from Senecio retrorsus 10 mg 300 Art. 6282.95 >95.0 % N [480-85-3] C8H13NO2 Mr 155.19

OH Retronecine N-oxide HPLC-DAD 5 mg 220 HO H Senecifolinene N-oxide with UV-Spectrum from Senecio retrorsus 10 mg 390

+ N Art. 6285.97 >97.0 % - [6870-33-3] O C8H13NO3 Mr 171.19

 Retrorsine 20 mg 150 HPLC-DAD HO CH2OH O 12,18-Dihydroxysenecionan-11,16-dione with UV-Spectrum H3C -Longilobin; from Senecio retrorsus 50 mg 295 CH3 O O O H Art. 6203.98 >98.0 % [480-54-6] N C18H25NO6 Mr 351.40

 HO CH2OH Retrorsine 100 mg 235 HPLC-DAD O 12,18-Dihydroxysenecionan-11,16-dione with UV-Spectrum H3C 500 mg 645 CH3 O -Longilobin; from Senecio retrorsus O O H Art. 6203.95 >95.0 % N [480-54-6] C18H25NO6 Mr 351.40

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

HO  CH2OH Retrorsine N-oxide 10 mg 150 O HPLC-DAD H3C 12,18-Dihydroxysenecionan-11,16-dione 4-oxide with UV-Spectrum CH3 O 20 mg 260 O O from Senecio retrorsus H Art. 6253.96 >96.0 % N [15503-86-3] O C18H25NO7 Mr 367.40

 Rhein 20 mg 100 HPLC-DAD OHO OH Cassic acid, Crysazin 3-carboxylic acid with UV-Spectrum from Rheum palmatum 50 mg 230 COOH Art. 3272.99 >99.0 % 100 mg 420 O [478-43-3] C15H8O6 Mr 284.23

 Rhein 250 mg 175 HPLC-DAD OHO OH Cassic acid, Crysazin 3-carboxylic acid with UV-Spectrum from Rheum palmatum COOH Art. 3272.97 >97.0 % O [478-43-3] C15H8O6 Mr 284.23

OH OH Rhein-8-O-glucoside HPLC-DAD 10 mg 155 OH Rhein 8-glucoside, 8-Glucosylrhein with UV-Spectrum O O O OH from Rheum palmatum 20 mg 260 HO Art. 3273.98 >98.0 % COOH [34298-86-7] O C21H18O11 Mr 446.37

HO CH2OH Riddelliine 10 mg 190 HPLC-DAD O H3C Riddeline, 18-Hydroxyseneciphylline with UV-Spectrum CH 2 O from Senecio riddellii O O H Art. 6312.98 >98.0 % N [23246-96-0] C18H23NO6 Mr 349.38

HO CH2OH Riddelliine N-oxide 10 mg 210 HPLC-DAD O H3C Riddeline N-oxide with UV-Spectrum CH 2 O from Senecio riddellii O O H Art. 6313.97 >97.0 % + N [75056-11-0] - O C18H23NO7 Mr 365.38

Rinderine 5 mg 370 H3C CH3 HPLC-DAD from Cynoglossum officinale with UV-Spectrum O CH3 HO H OH Art. 6310.95 >95.0 % O OH [6029-84-1] N C15H25NO5 Mr 299.36

Rinderine N-oxide 5 mg 370 H3C CH3 HPLC-DAD from Cynoglossum officinale with UV-Spectrum O CH3 HO H OH Art. 6311.95 >95.0 % O OH [137821-16-0] + N C15H25NO6 Mr 315.36 - O

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 Robinin 10 mg 145 HPLC-DAD OH Kaempferol 3-robinoside 7-rhamnoside with UV-Spectrum Rha-O O from Pseudoacacia 20 mg 229

O-Robinosyl Art. 3326.98 >98.0 % OH O [301-19-9] C33H40O19 Mr 740.67

 Rosmarinic acid 20 mg 240 O HPLC-DAD, TLC 1 13 HO OH from Rosmarinus officinalis H-NMR, C-NMR O 50 mg 435 H - (with Interpretation), HO OH Art. 6130.RS >99.0 % HOOC UV, IR, MS, Melting [20283-92-5] point, C18H16O8 Mr 360.32 content of water, content of residual solvents  Rosmarinic acid 20 mg 110 O HPLC-DAD HO OH from Rosmarinus officinalis with UV-Spectrum O 50 mg 220 H HO OH Art. 6130.99 >99.0 % HOOC [20283-92-5] C18H16O8 Mr 360.32

OH Ruberythric acid HPLC-DAD 5 mg 160 O OH O O O Alizarin-2-O-β-D-primveroside, Rubianic acid O OH with UV-Spectrum OH 10 mg 250 HO OH from Rubia tinctorum O OH Art. 3709.98 >98.0 % [152-84-1] C25H26O13 Mr 534.47

 Rutin 50 mg 120 OH HPLC-DAD HO O Rutoside, Quercetin 3-rutinoside, Sophorin with UV-Spectrum OH from Sophora japonica 100 mg 200 O-Glu-Rha OH O Art. 3256.99 >99.0 % [153-18-4] C27H30O16 Mr 610.52

CH 3 CH CH3 3 Ryanodine HPLC-DAD 1 mg 105 OH Ryanodol-3-(1H-pyrrole-2-carboxylate) H3C HO OH with UV-Spectrum HO 5 mg 395 O O from Ryania speciosa O H N HO CH3 Art. 6290.98 >98.0 % [15662-33-6] C25H35NO9 Mr 493.55

 OH Saponarin 10 mg 170 HPLC-DAD Glu-O O from Saponaria officinalis with UV-Spectrum 20 mg 280 Art. 3232.98 >98.0 % Glu OH O [20310-89-8] C27H30O15 Mr 594.53

 H3C HO CH3 HO Sceleratine 10 mg 250 HPLC-DAD O from Senecio retrorsus with UV-Spectrum HO CH 3 O Art. 6229.97 >97.0 % O O H [6190-25-6] C18H27NO7 Mr 369.41 N

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

H3C HO CH3 HO Sceleratine N-oxide 10 mg 250 HPLC-DAD O HO from Senecio retrorsus with UV-Spectrum CH3 O O O H Art. 6230.97 >97.0 % [103184-92-5] + C18H27NO8 Mr 385.41 N - O  HO CH3 Senecionine 20 mg 290 HPLC-DAD, GC-MS O 1 13 H3C Aureine, 12-Hydroxysenecionan-11,16-dione TLC, H-NMR, C- from Senecio vulgaris NMR 50 mg 600 CH3 O O O H - (with Interpretation), Art. 6202.RS >99.0 % UV, IR, MS, Melting [130-01-8] N point C18H25NO5 Mr 335.39  HO CH3 Senecionine 10 mg 145 HPLC-DAD O Aureine, 12-Hydroxysenecionan-11,16-dione with UV-Spectrum H3C 20 mg 225 CH3 O from Senecio vulgaris O O H Art. 6202.99 >99.0 % [130-01-8] N C18H25NO5 Mr 335.39

HO  CH3 Senecionine N-oxide 10 mg 230 O HPLC-DAD H3C 12-Hydroxysenecionan-11,16-dione 4-oxide with UV-Spectrum CH3 O O O from Senecio vulgaris H Art. 6252.97 >97.0 % N [13268-67-2] O C18H25NO6 Mr 351.39

HO Seneciphylline 20 mg 325 CH3 HPLC-DAD, GC-MS, O Jacodine, -Longilobine TLC, 1H-NMR, 13C- H3C from Senecio vulgaris NMR 50 mg 698 CH2 O O O - (with Interpretation), H Art. 6201.RS >99.0 % UV, IR, MS, Melting [480-81-9] point N C18H23NO5 Mr 333.38

HO CH3 Seneciphylline 10 mg 155 HPLC-DAD O Jacodine, -Longilobine with UV-Spectrum H3C 20 mg 272 CH2 O from Senecio vulgaris O O H Art. 6201.99 >99.0 % [480-81-9] N C18H23NO5 Mr 333.38

HO CH3 O Seneciphylline N-oxide 10 mg 258 HPLC-DAD H3C from Senecio vulgaris with UV-Spectrum CH2 O O O H Art. 6251.97 >97.0 % [38710-26-8] N C18H23NO6 Mr 349.37 O

 CH3 OH Senecivernine 5 mg 156 CH3 HPLC-DAD O from Senecio inaequidens with UV-Spectrum 10 mg 278 CH3 O O O Art. 6206.95 >95.0 % H [72755-25-0] C18H25NO5 Mr 335.39 N

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 CH3 OH CH3 Senecivernine N-oxide 5 mg 166 O HPLC-DAD from Senecio inaequidens with UV-Spectrum CH3 O 10 mg 300 O O H Art. 6220.95 >95.0 % [101687-28-9] N C18H25NO6 Mr 351.39

O

HO CH3 Senkirkin 10 mg 195 O HPLC-DAD H3C Senkirkine, Renardine with UV-Spectrum CH3 O from Tussilago farfara 20 mg 360 O O O Art. 6205.95 >95.0 % N [2318-18-5] CH3 C19H27NO6 Mr 365.43

OGlucO OH Sennoside A 10 mg 105 HPLC-DAD from Cassia angustifolia with UV-Spectrum 20 mg 140 COOH H H Art. 3280.98 >98.0 % COOH [81-27-6] 50 mg 288 C42H38O20 Mr 862.72

OGluc O OH

OGluc O OH Sennoside A1 10 mg 170 HPLC-DAD Sennoside G, Sennoside A‘ with UV-Spectrum 20 mg 242 COOH from Cassia angustifolia H H COOH Art. 3282.95 >95.0 % [66575-30-2] OGluc O OH C42H38O20 Mr 862.72

OGlucO OH Sennoside B 10 mg 105 HPLC-DAD from Cassia angustifolia with UV-Spectrum 20 mg 140 COOH H H Art. 3281.98 >98.0 % COOH [128-57-4] 50 mg 288 C42H38O20 Mr 862.72

OGluc O OH

OGluc O OH Sennoside C HPLC-DAD 10 mg 168 from Cassia angustifolia with UV-Spectrum CH2OH H H COOH Art. 3286.95 >95.0 % [37271-16-2] C42H40O19 Mr 848.76 OGluc O OH

[6]-Shogaol HPLC-DAD 10 mg 155

O 1-(4-Hydroxy-3-methoxyphenyl)-4-decen-3-one with UV-Spectrum

H3CO CH3 from Zingiber officinale HO Art. 4310.96 >96.0 % [555-66-8] C17H24O3 Mr 276.37

 Silybin 20 mg 102 HPLC-DAD O CH2OH Diastereomeric mixture of Silybin A and B with UV-Spectrum HO O OCH3 50 mg 214 O Silibinin, Silymarin I OH OH from Silybum marianum OH O Art. 3215.98 >98.0 % [22888-70-6] or [36804-17-8] C25H22O10 Mr 482.44

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

OH  Sinalbin 20 mg 130 HPLC-DAD O Sinapine glucosinalbate with UV-Spectrum HOH2C O S NOSO HO 50 mg 240 OH O from Sinapis alba HO

CH3O O N Art. 3409.99 >99.0 % HO O [20196-67-2]

CH O C30H42N2O15S2 Mr 734.79 3

 Sinalbin Potassium salt 20 mg 134 OH HPLC-DAD Glucosinalbin Potassium salt with UV-Spectrum 50 mg 260 O from Sinapis alba

HOH2C O S NOSO K HO OH O HO Art. 3410.97 >97.0 % [16411-05-5] C14H18NO10S2 K Mr 463.52

 OCH3 Sinensetin 10 mg 144 HPLC-DAD

CH3O O 3‘,4‘,5,6,7-Pentamethoxyflavone with UV-Spectrum OCH 3 from Orthosiphon stamineus 20 mg 252 CH3O OCH3 O Art. 3263.98 >98.0 % [2306-27-6] C20H20O7 Mr 372.38

 Sinigrin Monohydrate 50 mg 134 HPLC-DAD Sinigroside, Allylglucosinolate, with UV-Spectrum O Potassium myronate K Glucosyl-S N O S O from Sinapis nigra O Art. 3401.99 >99.0 % [3952-98-5]  C10H16KNO9S2 H2O Mr 415.48

 Sinigrin Monohydrate 1 g 210 HPLC-DAD Sinigroside, Allylglucosinolate, with UV-Spectrum O Potassium myronate Glucosyl-S N O S O K from Sinapis nigra O Art. 3401.97 >97.0 % [3952-98-5] C10H16KNO9S2  H2O Mr 415.48

 H3C H -Solanine 10 mg 110 CH 3 HPLC-DAD H N H C H 3 H CH3 alpha-Solanine, Solatunine with UV-Spectrum H CH2OH H 20 mg 173 CH2OH OH O O from Solanum tuberosum O O OH HO O 50 mg 345 OH Art. 6207.98 >98.0 % OH O [20562-02-1] CH3 OH OH C45H73NO15 Mr 868.40

H3C HO CH3 Spartioidine HPLC-DAD 5 mg 440 O (15E)-Seneciphyllin with UV-Spectrum from Senecio jacobea 2.5 mg 270 CH2 O O O H Art. 6314.95 >95.0 % [520-59-2] N C18H23NO5 Mr 333.38

 Spiraeoside 10 mg 129 O-Glu HPLC-DAD Quercetin 4‘-glucoside with UV-Spectrum HO O OH from Filipendula ulmaria 20 mg 225

OH OH O Art. 3257.98 >98.0 % [20229-56-5] C21H20O12 Mr 464.38

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 OH Sutherlandioside B 10 mg 161 HPLC-DAD from Sutherlandia frutescens with UV-Spectrum H O O 20 mg 286 H O OH HO Art. 5170.98 >98.0 % H [1055329-47-9] HOH OH HO OH C36H60O10 Mr 652.87

 OH Sutherlandioside D 10 mg 172 HPLC-DAD from Sutherlandia frutescens with UV-Spectrum H O O 20 mg 296 H O OH HO Art. 5171.95 >95.0 % H [1055329-49-1] H OH HO OH C36H58O9 Mr 634.84

 (+)-Taxifolin 20 mg 228 OH HPLC-DAD, TLC, Dihydroquercetin, Distylin 1H-NMR, 13C-NMR HO O 50 mg 325 OH from Pseudozuga menziesii - (with Interpretation), UV, IR, MS, Melting OH 100 mg 685 Art. 3211.RS >99.0 % point OH O [480-18-2]

C15H12O7 Mr 304.24

 (+)-Taxifolin 20 mg 110 OH HPLC-DAD Dihydroquercetin, Distylin with UV-Spectrum HO O 50 mg 255 OH from Pseudozuga menziesii OH Art. 3211.99 >99.0 % 100 mg 460 OH O [480-18-2]

C15H12O7 Mr 304.24

 Thesinine 5 mg 600 HPLC-DAD HO O 4-Hydroxycinnamoyloxy-1-methylpyrrolizidine with UV-Spectrum from Borago officinalis 1 mg 200 O H Art.-Nr. 6327.97 >97.0 % [488-02-8] N C17H21NO3 Mr 287.35

 Thesinine 4’-O-glucoside 5 mg 600 HPLC-DAD HO O O O with UV-Spectrum 1 mg 200 OH O HOHO from Borago officinalis H Art. 6328.97 >97.0 % N [460730-79-4] C23H31NO8 Mr 449.49

 HO HO Trichodesmine 5 mg 185 CH HPLC-DAD H3C 3 CH3 O from Crotalaria spec. with UV-Spectrum H3C 10 mg 330 CH3 O Art. 6322.98 >98.0 % O O H [548-90-3] C18H27NO6 Mr 353.41 N

 Trifolirhizin 10 mg 100 HPLC-DAD from Baptisia tinctoria with UV-Spectrum 20 mg 152 Art. 3225.96 >96.0 % [6807-83-6] C22H22O10 Mr 446.40

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 Umckalin HPLC-DAD 5 mg 135 HO O O 7-Hydroxy-5,6-dimethoxycoumarin with UV-Spectrum from Pelargonium sidoides 10 mg 226

CH3O Art. 3501.99 >99.0 % 20 mg 400 OCH3 [43053-62-9] C11H10O5 Mr 222.19

 CH3 Ursolic acid 20 mg 100 HPLC-DAD H C 3 (3)-3-Hydroxy-12-ursen-28-oic acid with UV-Spectrum from Arctostaphylos uva ursi 50 mg 200 H3C CH3 H COOH

H CH3 Art. 5121.99 >99.0 % HO H [77-52-1] H3C CH3 C30H48O3 Mr 456.71

H3C HO CH2OH Usaramine HPLC-DAD 10 mg 220 O (15E)-Retrorsine, Ursamine, Mucronatine with UV-Spectrum from Senecio retrorsus CH3 O O O H Art. 6315.96 >96.0 % [15503-87-4] N C18H25NO6 Mr 351.40

H C 3 HO CH OH 2 Usaramine N-oxide HPLC-DAD 10 mg 220 O (15E)-Retrorsine N-oxide with UV-Spectrum

CH3 O from Senecio retrorsus O O H Art. 6316.96 >96.0 % + N [117020-54-9] - C H NO M 367.40 O 18 25 7 r HPLC-DAD (2  CH3 Valerenic acid 25 mg 315 H methods), from Valeriana officinalis TLC (2 methods), 50 mg 500 1H-NMR, 13C-NMR Art. 4400.RS >99.0 % - (with Interpretation), CH [3569-10-6] 100 mg 845 3 CH3 UV, C H O M 234.34 15 22 2 r IR, MS, Melting point, COOH Elemental analysis, content of water, CH3 H Valerenic acid 10 mg 100 HPLC-DAD from Valeriana officinalis with UV-Spectrum 25 mg 200 Art. 4400.99 >99.0 % CH 3 CH3 [3569-10-6] 50 mg 345 C15H22O2 Mr 234.34 COOH 100 mg 615

 Verbascoside see Acteoside

OH HO OH  OH Vescalagin 10 mg 200 OH HPLC-DAD

O O from Castanea sativa with UV-Spectrum O OH 20 mg 374 O OH O O Art. 3312.96 >96.0 % HO O O O OH O [36001-47-5] HO OH C41H26O26 Mr 934.63 OH OH HO OH OH

OH  -Viniferin 10 mg 145 HPLC-DAD

OH trans-epsilon-Viniferin, (-)--Viniferin with UV-Spectrum from Vitis vinifera 20 mg 250 H OH Art. 3350.98 >98.0 % 50 mg 530 HO O H [62218-08-0] OH C28H22O6 Mr 454.48

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Catalogue of Natural Compounds

Structure Compound Documents Quantity Price delivered (unit) [Euro]

 OH Vitexin 10 mg 290 HPLC-DAD, TLC, Glu 8-Glucosylapigenin, Orientoside 1 13 HO O H-NMR, C-NMR from Crataegus monogyna - (with Interpretation), UV, IR, MS, Melting Art. 3234.RS >99.0 % point OH O [3681-93-4] C21H20O10 Mr 432.38

 OH Vitexin 5 mg 105 HPLC-DAD Glu 8-Glucosylapigenin, Orientoside with UV-Spectrum HO O from Crataegus monogyna 10 mg 155 Art. 3234.99 >99.0 % OH O [3681-93-4] C21H20O10 Mr 432.38

 Vitexin-2“-O-rhamnoside 10 mg 105 OH HPLC-DAD Glu-2"-O-Rha from Crataegus monogyna with UV-Spectrum HO O 20 mg 183 Art. 3236.99 >99.0 % [64820-99-1] OH O C27H30O14 Mr 578.53

 Wogonin 10 mg 100 H CO HPLC-DAD 3 5,7-Dihydroxy-8-methoxyflavone with UV-Spectrum HO O from Scutellaria baicalensis 20 mg 178 Art. 3213.97 >97.0 % OH O [632-85-9] C16H12O5 Mr 284.27

 Wogonoside 10 mg 160 HPLC-DAD Wogonin-7--D-glucopyranosiduronic acid with UV-Spectrum H CO HOOC 3 20 mg 277 O Wogonin 7-glucuronide, HO O O HO OH from Scutellaria baicalensis

OH O Art. 3214.97 >97.0 % [51059-44-0] C22H20O11 Mr 460.39

 Xanthohumol 20 mg 310 HPLC-DAD, TLC from Humulus lupulus 1H-NMR, 13C-NMR HO OH OH - (with Interpretation), 50 mg 580 Art. 3324.RS >99.0 % UV, IR, MS, Melting [6754-58-1] or [569-83-5] point, O O C21H22O5 Mr 354.40 content of water, H3C content of residual solvents

 Xanthohumol 10 mg 120 HPLC-DAD from Humulus lupulus with UV-Spectrum HO OH OH 20 mg 175 Art. 3324.99 >99.0 % [6754-58-1] or [569-83-5] 50 mg 355 O O C21H22O5 Mr 354.40 H3C

If you are interested in substances not listed above we will check the producibility and would be pleased to send you an individual offer.

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Please pay attention to the following information:

Update The catalogue may be updated several times a year. You can keep you informed about the actual version by visiting our website at www.phytoplan.de or by ordering a hardcopy per e-Mail: [email protected].

Delivery time Depending on the country abroad the delivery time will be 2-5 days. The promised delivery time is listed in the order confirmation. In case of ordering greater quantities there may be longer terms of delivery of about 2-5 weeks. But we will keep you informed in any case if there is a delay in supply.

Discount By ordering a single unit of the 5fold or 10fold quantity with respect to the greatest quantity listed we give you a discount of 10 percent or 15 percent respectively. If you are interested in bulk quantities we always will make you a special offer.

Shipment costs The actual shipment costs are outlined in the order confirmation.

Payment conditions Sale against payment in advance by Wire Transfer -toll free- to the following account: PHYTOPLAN Diehm & Neuberger GmbH Heidelberger Volksbank eG (Bank code 67 29 00 00) Account No. 22 59 06 77 Kurfürstenanlage 8, D-69115 Heidelberg, Germany For international wire transfers: BIC: GENODE61HD1 IBAN: DE67 6729 0000 0022590677 VAT ID: DE190955227

In case of order please indicate the substance, quality, item number and quantity you want to order. At least please send us the detailed shipping address inclusive postal code and the telephone number of a contact person.

page 52 

Certificate of Analysis using the example of the reference substance Kaempferol-3-glucoside, Art. 3242.RS

 PHYTOPLAN Diehm & Neuberger GmbH  PHYTOPLAN Diehm & Neuberger GmbH Im Neuenheimer Feld 519 Im Neuenheimer Feld 519 D-69120 Heidelberg D-69120 Heidelberg Tel.: 0 62 21/40 13 47 Tel.: 0 62 21/40 13 47 Pflanzliche Wirkstoffe und Analytik Fax: 0 62 21/43 76 64 Pflanzliche Wirkstoffe und Analytik Fax: 0 62 21/43 76 64

Analytical Report to the Certificate of Analysis (CA) CA-No.: 1051/1 CERTIFICATE OF ANALYSIS Date: 31.07.2001 Date: 31.07.2001 CA-No.: 1051/1 Kaempferol-3-glucoside Page: 1 of 15 Batch No.: 0107202 Product name: Kaempferol-3-glucoside Table of contents page Basic data Molecular formula 1. Manufacturing Procedure 2 Denotation: Kaempferol-3-glucoside Batch No.: 0107202 OH CAS-No.: [480-10-4] 2. Characteristics 2

Formula: C21H20O11 Molecular weight: 448.39 HO O 3. Melting Point 2 Storage temperature: 4 °C Source: Aesculus hippocastanum 4. TLC-Analysis 3 Stable until: July 2004 O-Glu Last purity control: July 2003 OH O 5. HPLC-Analysis 4 Date of manufacture: July 2001 Article No.: 3242.RS 6. 1H-NMR-Spectrum 6

DETERMINATION SPECIFICATION RESULT 7. 13C-NMR-Spectrum 9 Properties Appearance yellow needles conforms 8. FT-IR-Spectrum 11 Solubility soluble in hot methanol, low soluble in conforms water 9. UV-VIS-Spectrum 12 Identity Melting point 165-175 °C (methanol/water) 168-170 °C; conforms 10. FAB+-MASS Spectrum 13 NMR* 1H accordant to reference spectrum conforms 13 C accordant to reference spectrum conforms 11. Instrumentation 14 IR* consistent with structure conforms UV* accordant to reference spectrum conforms 12. References 15

max [nm] = 348, 265  2 max [nm] = 349.38; 265.52 log max = 4.20, 4.32  0.05 log max 4.21, 4.31 FAB-MS* molecular ion peak at m/z 449 [M+H]+ peak at m/z 449; conforms Purity TLC* 1 band 1 band; conforms HPLC* content of impurities at 254 nm: < 1.0 % 0.49 %; conforms at spectrum max plot: < 1.0 % 0.64 %; conforms Assay HPLC 99.0 % at 254 nm, Spectrum Max Plot 99.51, 99.36 %; conforms

Result: The product meets the requirements

Dr. M. Diehm (Quality Control)

 PHYTOPLAN Diehm & Neuberger GmbH  PHYTOPLAN Diehm & Neuberger GmbH Im Neuenheimer Feld 519 Im Neuenheimer Feld 519 D-69120 Heidelberg D-69120 Heidelberg Tel.: 0 62 21/40 13 47 Tel.: 0 62 21/40 13 47 Pflanzliche Wirkstoffe und Analytik Fax: 0 62 21/43 76 64 Pflanzliche Wirkstoffe und Analytik Fax: 0 62 21/43 76 64

Analytical Report to the Certificate of Analysis (CA) CA-No.: 1051/1 Analytical Report to the Certificate of Analysis (CA) CA-No.: 1051/1 Date: 31.07.2001 Date: 31.07.2001 Kaempferol-3-glucoside Page: 2 of 15 Kaempferol-3-glucoside Page: 3 of 15 Batch No.: 0107202 Batch No.: 0107202

1. Manufacturing Procedure 4. TLC-Analysis Kaempferol-3-glucoside was isolated from the blooms of aesculus hippocastanum by an extraction process with Parameters methanol and ethyl acetate. A pure product was obtained by preparative column chromatography on an RP18- Stationary phase: Silica gel 60 F254, 0.20 mm thickness (Art.-No. 1.05554, Merck, Darmstadt, Ger.) phase with methanol / water as eluent. The substance was crystallized from methanol / water (9:1) and dried at Mobile phase: Ethyl acetate / Formic acid / Water (20/2/3; v/v/v) 40 °C / 10 mbar over a period of 24 hours. Sample solvent: Methanol Development length: 10 cm

Retention factor: Rf = 0.54 (chamber saturation) 2. Characteristics Detection: UV254, Diphenylboryloxyethylamine (Naturstoffreagenz A), 10 % in ethanol, Kaempferol-3-glucoside is stable to moisture and air and has only low tendency to be hydrolysed or to be after drying spraying with macrogel 400 / 10 min. at 110 °C; visualized at UV365 oxidized. No hygroscopy was observed. In order to prevent any decompositon it should be stored at a dry place Applied quantities: 20, 10 µg in a refrigerator. Chromatogram: 1 spot with one very weak impurity below at Rf = 0.49 (UV365) Reference: Hyperoside

3. Melting Point TLC-Chromatogram (1:1) Found: 168-170 °C (water / methanol 9:1)

[1] Ref. : 177-178°C (methanol) Rf / dm 1.0

0.9

0.8 0.7 0.6 Trace 1: Hyperoside Trace 2 + 3 : Kaempferol-3- 0.5 glucoside, 20 µg, 10 µg; after spraying with 0.4 Naturstoffreagenz A 0.3

0.2

0.1 0.0

page 53 

Certificate of Analysis using the example of the reference substance Kaempferol-3-glucoside, Art. 3242.RS

 PHYTOPLAN Diehm & Neuberger GmbH  PHYTOPLAN Diehm & Neuberger GmbH Im Neuenheimer Feld 519 Im Neuenheimer Feld 519 D-69120 Heidelberg D-69120 Heidelberg Tel.: 0 62 21/40 13 47 Tel.: 0 62 21/40 13 47 Pflanzliche Wirkstoffe und Analytik Fax: 0 62 21/43 76 64 Pflanzliche Wirkstoffe und Analytik Fax: 0 62 21/43 76 64

Analytical Report to the Certificate of Analysis (CA) CA-No.: 1051/1 Analytical Report to the Certificate of Analysis (CA) CA-No.: 1051/1 Date: 31.07.2001 Date: 31.07.2001 Kaempferol-3-glucoside Page: 4 of 15 Kaempferol-3-glucoside Page: 5 of 15 Batch No.: 0107202 Batch No.: 0107202

5. HPLC-Analysis 4: 355 nm, 4 nm Column Typ: Eurospher 100-5 C18, 250 x 4 mm with integrated precolumn 5 x 4 mm Pk # Retention Time Area Area Percent Capacity factor Lambda Max Sample solvent: Methanol 1 6,453 7052 0,14 2,23 259 Mobile phase: Methanol/Acetonitrile/Orthophosphoric acid pH 2.5 (34/10/56, v/v/v) 2 8,448 5566 0,11 3,22 211 3 9,333 4861505 99,57 3,67 265 Detection: DAD, 210-450 nm 4 10,752 8572 0,18 4,38 212 Injection vol.: 5 µL, c = 0.5 mg/mL Totals 4882695 100,00 Flow rate: 1.00 mL/min.

Temperature: 20 °C ) Spectrum Max Plot* Pk # Retention Time Area Area Percent Capacity factor Lambda Max 300 2: 254 nm, 4 nm Spectrum Max Plot Kaempferol-3-glucosid Ch.-B.: 0107202 Kaempferol-3-glucosid Ch.-B.: 0107202 1 4,661 11299 0,14 1,33 217 Kaempferol3glc02RPmet4-005.dat 500 Kaempferol3glc02RPmet4-005.dat Retention Time Retention Time 2 6,453 14319 0,17 2,23 252 3 8,437 9885 0,12 3,22 213 9,333 250 9,333 4 9,333 8295465 99,36 3,67 265 5 10,731 18038 0,22 4,37 217 400 Totals 8349006 100,00 200 *) A Spectrum Max Plot is a chromatogram with each point plotted at its maximum absorbance. within the detection range

300 This plot gives an indication of the appearance of the chromatogram when the wavelengths are optimized for each peak.

150 mAU DAD UV-spectrum

200 100

100 50

6,453 10,731 6,464 8,459 10,784 4,661 8,437 0 0 0 10 20 0 10 20 Minutes Minutes 2: 254 nm, 4 nm Pk # Retention Time Area Area Percent Capacity factor Lambda Max 1 6,464 8515 0,18 2,23 257 2 8,459 5169 0,11 3,23 212 3 9,333 4726060 99,51 3,67 265 4 10,784 9453 0,20 4,39 214 Totals 4749197 100,00

5: 265 nm, 4 nm Pk # Retention Time Area Area Percent Capacity factor Lambda Max 1 6,443 7671 0,13 2,22 257 2 8,448 6651 0,11 3,22 265 3 9,333 6021564 99,62 3,67 265 The UV-spectrum recorded with HPLC-DAD at time 9.33 min. is consistant with the UV-spectrum of the 4 10,752 8753 0,14 4,38 212 isolated substance. Totals 6044639 100,00

 PHYTOPLAN Diehm & Neuberger GmbH  PHYTOPLAN Diehm & Neuberger GmbH Im Neuenheimer Feld 519 Im Neuenheimer Feld 519 D-69120 Heidelberg D-69120 Heidelberg Tel.: 0 62 21/40 13 47 Tel.: 0 62 21/40 13 47 Pflanzliche Wirkstoffe und Analytik Fax: 0 62 21/43 76 64 Pflanzliche Wirkstoffe und Analytik Fax: 0 62 21/43 76 64

Analytical Report to the Certificate of Analysis (CA) CA-No.: 1051/1 Analytical Report to the Certificate of Analysis (CA) CA-No.: 1051/1 Date: 31.07.2001 Date: 31.07.2001 Kaempferol-3-glucoside Page: 6 of 15 Kaempferol-3-glucoside Page: 7 of 15 Batch No.: 0107202 Batch No.: 0107202 6. 1H-NMR-Spectrum 1H-NMR-Spectrum 300 MHz, 297 K, solvent: DMSO-d6 Peak List

Peak no Point ppm Frequency (Hz) Height 1 5562 12.615 3786.298 31.957 2 13010 8.053 2417.001 20.649 3 13020 8.047 2415.231 6.195 4 13030 8.041 2413.433 1.677 5 13058 8.024 2408.226 22.744 6 13072 8.015 2405.679 2.719 7 14898 6.897 2069.924 21.729 8 14920 6.883 2065.969 1.733 9 14948 6.866 2060.671 21.903 10 15652 6.435 1931.239 16.198 11 15662 6.429 1929.564 14.782 12 16020 6.209 1863.668 16.893 13 16032 6.202 1861.490 15.684 14 17226 5.470 1641.880 9.302 15 17264 5.447 1634.924 9.091 16 17434 5.343 1603.761 7.577 17 17458 5.329 1599.297 7.794 18 17906 5.054 1517.011 5.768 19 17930 5.039 1512.515 5.966 20 18084 4.945 1484.314 4.300 21 19180 4.274 1282.791 3.266 22 19210 4.256 1277.294 6.910 23 19240 4.237 1271.781 3.033 24 20294 3.591 1077.920 2.900 25 20320 3.576 1073.166 3.168 26 20352 3.556 1067.300 3.658 27 20382 3.538 1061.774 3.624 28 20888 3.228 968.804 1.514 29 20914 3.212 963.891 3.200 30 20934 3.199 960.206 5.344 31 20954 3.188 956.681 4.687 32 20970 3.178 953.711 3.822 33 20994 3.163 949.200 3.991 34 21128 3.080 924.523 9.123

page 54 

Certificate of Analysis using the example of the reference substance Kaempferol-3-glucoside, Art. 3242.RS

 PHYTOPLAN Diehm & Neuberger GmbH  PHYTOPLAN Diehm & Neuberger GmbH Im Neuenheimer Feld 519 Im Neuenheimer Feld 519 D-69120 Heidelberg D-69120 Heidelberg Tel.: 0 62 21/40 13 47 Tel.: 0 62 21/40 13 47 Pflanzliche Wirkstoffe und Analytik Fax: 0 62 21/43 76 64 Pflanzliche Wirkstoffe und Analytik Fax: 0 62 21/43 76 64

Analytical Report to the Certificate of Analysis (CA) CA-No.: 1051/1 Analytical Report to the Certificate of Analysis (CA) CA-No.: 1051/1 Date: 31.07.2001 Date: 31.07.2001 Kaempferol-3-glucoside Page: 8 of 15 Kaempferol-3-glucoside Page: 9 of 15 Batch No.: 0107202 Batch No.: 0107202

13 1H-NMR-Spectrum 7. C-NMR-Spectrum

300 MHz, 297 K, solvent: DMSO-d6 75 MHz, 297 K, solvent: DMSO-d6

5' OH 6' 4' 8 1 HO 2 O 3' 1' 7 9 2' 4" 2" OH OH 6 10 3" HO 3 O O 5 4 CH2OH 6" OH O 1" 5"

Assignment of the signals [500 MHz, solvent: CDCl3, temperature: 303 K]

Assignment of the signals

Proton at Chemical shift Comparison data[1] Solvent-signals, C-Atom OH-signals

6 6.21, d (2.0 Hz) 6.21, d (2.0 Hz) 2.50 (DMSO) 8 6.43, d (2.0 Hz) 6.44, d (2.0 Hz) 3.33 (water signal of the 2'' 8.04, d (8.8 Hz) 8.04, d (8.8 Hz) solvent) 3'' 6.88, d (9.4 Hz) 6.88, d (8.8 Hz) 5.33, 5.04, 4.93, 4.25 5' 6.88, d (9.4 Hz) 6.88, d (8.8 Hz) (OH-signals), 6'' 8.04, d (8.8 Hz) 8.04, d (8.8 Hz) 12.62 (OH-O hydrogen bridge) 1" 5.46, d (7.3 Hz) 5.45, d (7.4 Hz) 2" 3.08-3.19 m no data cited 3" 3.08-3.19 m 4" 3.08-3.19 m 5" 3.08-3.19 m 6"A 3.08-3.19 m 6"B 3.55, dd (5.0 Hz, 11.5 Hz)

The assignment was performed with the help of the data given in Ref.[1].

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Analytical Report to the Certificate of Analysis (CA) CA-No.: 1051/1 Analytical Report to the Certificate of Analysis (CA) CA-No.: 1051/1 Date: 31.07.2001 Date: 31.07.2001 Kaempferol-3-glucoside Page: 10 of 15 Kaempferol-3-glucoside Page: 11 of 15 Batch No.: 0107202 Batch No.: 0107202

13 C-NMR-Spectrum 8. FT-IR-Spectrum 75 MHz, 297 K, solvent: DMSO-d6 KBr-Pellet

5' OH 6' 4' 8 1 HO O 2 3' 1' 7 9 2' 4" 2" OH 10 3" OH 6 HO 3 O O 5 4 CH2OH 6" OH O 1" 5"

Assignment of the signals

C-Atom Chemical shift Comparison data[3] Solvent-signals

2 156.4 156.3 38.7 – 40.4 (DMSO) 3 133.3 133.0 4 177.5 177.5 5 161.2 161.1 6 98.7 98.7 7 164.1 164.1 8 93.7 93.6 9 156.3 156.3 No cm-1 %T Intensity No cm-1 %T Intensity 10 104.1 104.1 1 554.00 74.025 W 15 1246.00 67.923 M 1' 121.0 121.0 2 584.00 72.624 W 16 1286.00 56.564 M 3 636.00 71.563 M 17 1353.00 52.707 S 2'' 130.9 130.7 4 657.00 72.603 W 18 1442.00 60.393 M 3'' 115.1 115.0 5 797.00 73.287 W 19 1466.00 69.857 M 4'' 160.0 159.8 6 837.00 76.953 W 20 1506.00 53.644 M 5' 115.1 115.0 7 965.00 78.205 W 21 1558.00 59.498 M 6' 130.9 130.7 8 993.00 68.545 M 22 1579.00 64.324 M 1'' 101.0 101.4 9 1017.00 54.019 M 23 1607.00 46.474 S 2'' 74.3 74.2 10 1066.00 49.720 S 24 1649.00 48.716 S 3'' 76.5 76.5 11 1091.00 66.601 M 25 2897.00 60.715 M 4'' 70.0 70.1 12 1112.00 67.983 M 26 2920.00 60.451 M 13 1181.00 43.075 S 27 3435.00 27.065 VS 5'' 77.5 77.2 14 1220.00 64.828 M 28 3524.00 34.486 S 6'' 60.9 61.0

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Certificate of Analysis using the example of the reference substance Kaempferol-3-glucoside, Art. 3242.RS

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Analytical Report to the Certificate of Analysis (CA) CA-No.: 1051/1 Analytical Report to the Certificate of Analysis (CA) CA-No.: 1051/1 Date: 31.07.2001 Date: 31.07.2001 Kaempferol-3-glucoside Page: 12 of 15 Kaempferol-3-glucoside Page: 13 of 15 Batch No.: 0107202 Batch No.: 0107202 9. UV-VIS-Spectrum 10. FAB+-MASS Spectrum Solvent: Methanol (UVASOL, Merck) Conc.: 6.7x10-5 mol/l

Result

Maxima: max [nm] log max Minima: min [nm] log min

349.38 4.21 282.17 3.99 Result 265.52 4.31 240.55 4.10 The measurement technic of the FAB+-MS mode leads to the molecule ions [M+H]+ and [M+Na]+. The peaks at m/z 449 (448+1) and m/z 471 (448+23) show the expected molecular mass (448) of Kaempferol-3- [1] Data given in Ref. : max [nm] log : 348.7 (4.20), 265.5 (4.35). glucosid. Most other detected peaks derived from the NBA-matrix.

 PHYTOPLAN Diehm & Neuberger GmbH  PHYTOPLAN Diehm & Neuberger GmbH Im Neuenheimer Feld 519 Im Neuenheimer Feld 519 D-69120 Heidelberg D-69120 Heidelberg Tel.: 0 62 21/40 13 47 Tel.: 0 62 21/40 13 47 Pflanzliche Wirkstoffe und Analytik Fax: 0 62 21/43 76 64 Pflanzliche Wirkstoffe und Analytik Fax: 0 62 21/43 76 64

Analytical Report to the Certificate of Analysis (CA) CA-No.: 1051/1 Analytical Report to the Certificate of Analysis (CA) CA-No.: 1051/1 Date: 31.07.2001 Date: 31.07.2001 Kaempferol-3-glucoside Page: 14 of 15 Kaempferol-3-glucoside Page: 15 of 15 Batch No.: 0107202 Batch No.: 0107202

11. Instrumentation 12. References

[1] T. Sekine et al., Chem. Pharm. Bull., 1993, 41(6), 1185-87. Determination Apparatus [2] K. R. Markham, T. J. Marbry, Carbon-13 NMR Studies of -III, Melting Point MEL-TEMP II apparatus, Laboratory Devices, USA Tetrahedron, 1978, 34, 1389-97.

HPLC-Analysis Pump: Shimadzu LC-10ADvp Detector (DAD): Shimadzu SPD-M10Avp Injector: Rheodyne 7725i, 10 µL loop

1H-NMR-Spectrum Bruker AM 300

13C-NMR-Spectrum Bruker AM 300 UV-VIS-Spectrum Varian CARY 2300 Spectralphotometer FT-IR-Spektrum FT-IR-Spectrometer 1760X Perkin-Elmer FAB+-MASS Spectrum JEOL JMS-700

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