DOCSLIB.ORG

Chemical Name CAS RN Molecular Formula Specific Sops (-)-2Β

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Chemical Name CAS RN Molecular Formula Specific Sops (-)-2Β Chemical Name CAS RN Molecular Formula Specific SOPs (-)-2β-Carbomethoxy-3β-(4-fluorophenyl)tropane 50370-56-4 C16H20FNO2 Acutely Toxic Materials, (1) (-)-alpha-Santonin 481-06-1 C15H18O3 Acutely Toxic Materials, (1) (-)-Bebeerine 436-05-5 C36H38N2O6 Acutely Toxic Materials, (1) (-)-Delta9-Tetrahydrocannabinol solution 1972-08-3 C21H30O2 (-)-Deoxyephedrine 33817-09-3 C10H15N (-)-DIP-Chloride(TM) solution 85116-37-6 C22H38BCl (-)-Epibatidine-L-tartrate 152378-30-8 C11H13ClN2 · C4H6O6 Acutely Toxic Materials, (1) (-)-Epinephrine 51-43-4 C9H13NO3 Acutely Toxic Materials, (1) (-)-Epinephrine (+)-bitartrate salt 51-42-3 C13H19NO9 Acutely Toxic Materials, (1) (-)-Huperzine A 102518-79-6 C15H18N2O Acutely Toxic Materials, (1) (-)-Nicotine 54-11-5 C10H14N2 Acutely Toxic Materials, (1) (-)-Nicotine hydrogen tartrate salt 65-31-6 C18H26N2O12 Acutely Toxic Materials, (1) (-)-Norepinephrine 51-41-2 C8H11NO3 Acutely Toxic Materials, (1) (-)-Norgestrel 797-63-7 C21H28O2 (-)-Scopolamine hydrobromide hydrate 114-49-8 C17H21NO4 · HBr · 3H2O Acutely Toxic Materials, (1) (-)-Scopolamine hydrobromide trihydrate 6533-68-2 C17H28BrNO7 Acutely Toxic Materials, (1) (-)-Scopolamine hydrochloride 55-16-3 C17H22ClNO4 Acutely Toxic Materials, (1) (-)Scopolamine methyl nitrate 6106-46-3 C18H24N2O7 Acutely Toxic Materials, (1) (-)-Thalidomide 841-67-8 C13H10N2O4 (-)-α-Methylphenethylamine sulfate 51-62-7 (C9H13N)2.H2SO4 Acutely Toxic Materials, (1) (+)-2,2'-Isopropylidenebis[(4R)-4-phenyl-2-oxazoline] 150529-93-4 C21H22N2O2 Acutely Toxic Materials, (1) (+)-2-Fluoro-4-(5,6,7,8-tetrahydro-imidazo[1,5-a]pyridin-8-yl)benzonitrile ? C14H12FN3 Acutely Toxic Materials, (1) (+)-4-(5,6,7,8-Tetrahydro-imidazo[1,5-a]pyridin-8-yl)benzonitrile ? C14H13N3 Acutely Toxic Materials, (1) (+)-Bicuculline 485-49-4 C20H17NO6 Acutely Toxic Materials, (1) (+)-Biotin 4-nitrophenyl ester 33755-53-2 (+)-Digitoxigenin 143-62-4 Acutely Toxic Materials, (1) (+)-Emetine dihydrochloride hydrate 313222-95-6 Acutely Toxic Materials, (1) (+)-Epibatidine dihydrochloride 166374-43-2 Acutely Toxic Materials, (1) (+)-Griseofulvin 126-07-8 (+)-Muscarine chloride 2303-35-7 Acutely Toxic Materials, (1) (+)-Thalidomide 2614-06-4 (+)-Valinomycin 2001-95-8 Acutely Toxic Materials, (1) (+/-)-(E)-4-Ethyl-2-[(E)-hydroxyimino]-5-nitro-3-hexenamide 138472-01-2 (+/-)-(E)-4-Ethyl-2-[(Z)-hydroxyimino]-5-nitro-3-hexen-1-yl-nicotinamide 162626-99-5 (+/-)-1-(2,5-Dimethoxyphenyl)-2-aminopropane hydrochloride 2801-68-5 Acutely Toxic Materials, (1) (+/-)-2,5-Dimethoxy-4-bromoamphetamine hydrobromide 53581-53-6 Acutely Toxic Materials, (1) (+/-)-2-Chloropropionic acid 598-78-7 Acutely Toxic Materials, (1) (+/-)-3-Chloro-1,2-propanediol 96-24-2 Acutely Toxic Materials, (1) (+/-)-5-Hydroxy-(6E,8Z,11Z,14Z)-eicosatetraenoic acid delta-lactone 73279-37-5 (+/-)-6-Hydroxy-3,4-methylenedioxymethamphetamine 138808-79-4 Acutely Toxic Materials, (1) (+/-)Amethopterin hydrate 60388-53-6 (+/-)-Anabasine 13078-04-1 Acutely Toxic Materials, (1) (+/-)-Baclofen 1134-47-0 (+/-)-Bay K8644 71145-03-4 (+/-)-Cloprostenol sodium salt hydrate 55028-72-3 (+/-)-Deoxyephedrine hydrochloride 300-42-5 Acutely Toxic Materials, (1) (+/-)deoxyephedrine, methanol solution 67-56-1 Potential Reproductive Hazard, (1) (+/-)-Deoxyephedrine-d5 hydrochloride 60124-81-4 (+/-)-Epibatidine dihydrochloride hydrate Lookup Failed C11H13ClN2 · 2HCl · xH2O Acutely Toxic Materials, (1) (+/-)-Epichlorohydrin 106-89-8 Carcinogens, (1) (+/-)-Indoline-2-carboxylic acid 78348-24-0 (+/-)-Lorazepam 846-49-1 (+/-)-Methadone hydrochloride 1095-90-5 Acutely Toxic Materials, (1) (+/-)-Nicotine 22083-74-5 Acutely Toxic Materials, (1) (+/-)-Norepinephrine (+)-bitartrate salt 3414-63-9 Acutely Toxic Materials, (1) (+/-)-Propylene oxide 75-56-9 Carcinogens, (1) (+/-)-Quinuclidinyl benzilate 6581062 C21H23NO3 Acutely Toxic Materials, (1) (+/-)-Thalidomide 50-35-1 (±)-1-(4-Bromo-2,5-dimethoxyphenyl)-2-ethanamine hydrochloride 66142-81-2 Acutely Toxic Materials, (1) (±)-2,5-Dimethoxy-4-bromoamphetamine hydrobromide 53581-53-6 Acutely Toxic Materials, (1) (±)-2-Chloropropionic acid 598-78-7 Acutely Toxic Materials, (1) (±)-2-Ethylhexanoic acid 149-57-5 (±)-Baclofen 1134-47-0 (±)-Epinephrine methyl ether hydrochloride 103213-56-5 (±)-Glycidol 556-52-5 (±)-Methamphetamine hydrochloride 300-42-5 Acutely Toxic Materials, (1) (±)-Nicotine-d3 salicylate salt 1173021-00-5 Acutely Toxic Materials, (1) (1-(5-Bromo-3-nitropyridin-2-yl)pyrrolidin-3-yl)methanol 1138444-02-6 (1,2-Bis[diphenylphosphino]ethane)dichloronickel(II) 14647-23-5 (1,3-Dioxan-2-ylethyl)magnesium bromide 480438-44-6 C6H11BrMgO2 Grignard Reagents, (1) (1,3-Dioxolan-2-ylmethyl)magnesium bromide 180675-22-3 C4H7BrMgO2 Grignard Reagents, (1) (1,3-Dioxolan-2-ylmethyl)zinc bromide 1135389-59-1 C4H7BrO2Zn Zinc Alkyl Reagents, (1) (11bR, 11'bR)-4,4'-(Oxydi-2,1-phenylene)bis-dinaphtho[2,1-d:, 1', 2'-f][1,3,2]dioxaphosphepi 391860-55-2 (11bS, 11'bS)-4,4'-(Oxydi-2,1-phenylene)bis-dinaphtho[2,1-d: 1', 2'-f][1,3,2]dioxaphosphepin 898830-89-2 (1-Boc-7-azaindol-3-methyl)trimethylammonium iodide 144866-90-0 Acutely Toxic Materials, (1) (1e)-N'-hydroxy-2-(1H-1,2,4-triazol-1-yl)ethanimidamide (1R)-Camphor oxime 2792-42-9 (1R,2R)-(-)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol 716-61-0 (1R,2R)-(-)-N-Boc-2-amino-1-(4-nitrophenyl)-1,3-propanediol 366487-74-3 (1R,3S,4S)-N-Boc-2-azabicyclo[2.2.1]heptane-3-carboxylic acid 291775-59-2 (1R,E)-(+)-Camphorquinone 3-oxime 31571-14-9 (1S, 2S)-1,2-Bis(4-nitrophenyl)ethylenediamine dihydrochloride 1052707-07-9 (1S,2S)-(+)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol 2964-48-9 (1S,2S)-N,N'-Dihydroxy-N,N'-bis(bis(3,5-dimethylphenyl)acetyl)-1,2-cyclohexanediamine 1217463-44-9 Acutely Toxic Materials, (1) (1S,2S)-N,N'-Dihydroxy-N,N'-bis(diphenylacetyl)-1,2-cyclohexanediamine 1217464-22-6 Acutely Toxic Materials, (1) (1S,E)-(-)-Camphorquinone 3-oxime 251645-83-7 (1Z)-2-(Diethylamino)-N'-hydroxyethanimidamide (1z)-2-(dimethylamino)-N'-hydroxyethanimidamide (1z)-3-(1H-benzimidazol-1-yl)-N'-hydroxypropanimidamide (1z)-3-(5,6-dimethyl-1H-benzimidazol-1-yl)-N'-hydroxypropanimidamide (1z)-3-[(4-chlorophenyl)sulfanyl]-N'-hydroxypropanimidamide (1Z)-N',3-Dihydroxypropanimidamide 53370-50-6 (1z)-N'-hydroxy-2-(1-methyl-1H-benzimidazol-2-yl)ethanimidamide (1Z)-N'-Hydroxy-2-methylbutanimidamide hydrochloride (2,2')-Furildioxime 522-27-0 (24R)-24,25-Dihydroxyvitamin D3 55721-11-4 Acutely Toxic Materials, (1) (24S)-24,25-Dihydroxyvitamin D3 55700-58-8 Acutely Toxic Materials, (1) (2-Chloro-5-pyridyl)methylzinc chloride 352530-36-0 C6H5Cl2NZn Zinc Alkyl Reagents, (1) (2-Ethylhexl)magnesium bromide 90224-21-8 C8H17BrMg Grignard Reagents, (1) (2-Naphthalenylmethyl)magnesium bromide 127543-80-0 C11H9BrMg Grignard Reagents, (1) (2-Naphthylmethyl)zinc bromide 152329-44-7 C11H9BrZn Zinc Alkyl Reagents, (1) (2-Nitrophenoxy)acetyl chloride (2R)-(-)-2-Methylglycidyl 4-nitrobenzoate 106268-96-6 (2R)-(-)-Glycidyl 4-nitrobenzoate 106268-95-5 (2R)-(-)-Glycidyl tosylate 113826-06-5 (2R)-(+)-3,3-Dimethylglycidyl 4-nitrobenzoate 141700-91-6 (2R,3R)-(+)-3-(4-Nitrophenyl)glycidol 37141-32-5 (2R,3S)-(+)-3-(Benzyloxymethyl)oxirane-2-methanol 4-nitrobenzoic acid ester 78469-86-0 (2S)-(+)-2-Methylglycidyl 4-nitrobenzoate 118200-96-7 (2S)-(+)-Glycidyl 3-nitrobenzenesulfonate 115314-14-2 (2S)-(+)-Glycidyl 4-nitrobenzoate 115459-65-9 (2S)-(+)-Glycidyl tosylate 70987-78-9 (2S,3R)-(-)-3-(Benzyloxymethyl)oxirane-2-methanol 4-nitrobenzoic acid ester 78513-08-3 (2S,3S)-(-)-3-(4-Nitrophenyl)glycidol 1885-07-0 (2S,3S)-trans-3-Methyloxirane-2-methyl 4-nitrobenzoate 106268-97-7 (2S,3S)-trans-3-Phenyl-2-oxiranylmethyl 4-nitrophenyl carbonate 147349-28-8 (2z)-2-amino-N-(4-chlorophenyl)-2-(hydroxyimino)ethanamide (3,5-Dimethyl-4-nitro-2-pyridyl)-1-methanol 149082-03-1 (3?5?)-3-[(O-?-D-Glucopyranosyl-(1?6)-O-?-D-glucopyranosyl-(1?4 )-2 ,6-dideoxy-3-O-methy 33279-57-1 Acutely Toxic Materials, (1) (3aR,7aR)-2-Dimethylamino-1,3-dimethyl-octahydro-1H-1,3,2-benzodiazaphosphole solution91633-80-6 (3-fluoro-4-nitro-phenyl)-methanol (3-Nitrobenzyl)mercaptan 77472-39-0 (3-Nitrophenyl)methanesulfonyl chloride (3'-Nitropropiophenone) 17408-16-1 (3R)-(+)-3-(1-Methyl-1H-indol-3-yl)butanenitrile 429689-23-6 Acutely Toxic Materials, (1) (3S)-(-)-3-(1-Methyl-1H-indol-3-yl)butanenitrile 429689-24-7 Acutely Toxic Materials, (1) (3z)-3-amino-N-(3,5-dichlorophenyl)-3-(hydroxyimino)propanamide (3z)-3-amino-N-(4-fluorophenyl)-3-(hydroxyimino)propanamide (3z)-7-methyl-1H-indole-2,3-dione 3-oxime (4-(1-Piperidinylmethyl)phenyl)magnesium bromide 480424-83-7 C12H16BrMgN Grignard Reagents, (1) (4,5,6,7-Tetrachloro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetic acid Lookup Failed C10H3Cl4NO4 Acutely Toxic Materials, (1) (4-Nitrobenzyl)mercaptan 26798-33-4 (4-Nitrobenzyl)trimethylammonium chloride 5350-96-9 (4-Nitrobenzyl)triphenylphosphonium bromide 2767-70-6 (4-Nitrophenyl)(2,4,6-trimethylphenyl)iodonium triflate 1146127-11-8 (4-nitrophenyl)methanesulfonyl chloride (4-Nitrophenyl)phenyliodonium triflate 905718-45-8 (5-nitro-pyridin-2-ylsulfanyl)-acetic acid (5α)-4,5-Epoxy-3,14-dihydroxy-17-methylmorphinan-6-one hydrochloride monohydrate 357-07-3 Acutely Toxic Materials, (1) (Acetylacetonato)dicarbonyliridium(I) 14023-80-4 (Chloromethylene)dimethyliminium chloride 3724-43-4 (Cyclohexylmethyl)magnesium bromide 35166-78-0 C7H13BrMg Grignard Reagents, (1) (Cyclohexylmethyl)zinc bromide 135579-86-1 C7H13BrZn Zinc Alkyl Reagents, (1) (Dimethylamino)acetonitrile 926-64-7 Acutely Toxic Materials, (1) (Dimethylamino)trimethyltin(IV) 993-50-0 Acutely Toxic Materials, (1) (E)-1,5-Naphthyridine-3-carbaldehyde
Load more

Recommended publications
  • Restricted Use Product Summary Report
    Page 1 of 17 Restricted Use Product Summary Report (January 19, 2016) Percent Active Registration # Name Company # Company Name Active Ingredient(s) Ingredient 4‐152 BONIDE ORCHARD MOUSE BAIT 4 BONIDE PRODUCTS, INC. 2 Zinc phosphide (Zn3P2) 70‐223 RIGO EXOTHERM TERMIL 70 VALUE GARDENS SUPPLY, LLC 20 Chlorothalonil 100‐497 AATREX 4L HERBICIDE 100 SYNGENTA CROP PROTECTION, LLC 42.6 Atrazine 100‐585 AATREX NINE‐O HERBICIDE 100 SYNGENTA CROP PROTECTION, LLC 88.2 Atrazine 100‐669 CURACRON 8E INSECTICIDE‐MITICIDE 100 SYNGENTA CROP PROTECTION, LLC 73 Profenofos 100‐817 BICEP II MAGNUM HERBICIDE 100 SYNGENTA CROP PROTECTION, LLC 33; 26.1 Atrazine; S‐Metolachlor 100‐827 BICEP LITE II MAGNUM HERBICIDE 100 SYNGENTA CROP PROTECTION, LLC 28.1; 35.8 Atrazine; S‐Metolachlor 100‐886 BICEP MAGNUM 100 SYNGENTA CROP PROTECTION, LLC 33.7; 26.1 Atrazine; S‐Metolachlor 100‐898 AGRI‐MEK 0.15 EC MITICIDE/INSECTICIDE 100 SYNGENTA CROP PROTECTION, LLC 2 Abamectin 100‐903 DENIM INSECTICIDE 100 SYNGENTA CROP PROTECTION, LLC 2.15 Emamectin benzoate 100‐904 PROCLAIM INSECTICIDE 100 SYNGENTA CROP PROTECTION, LLC 5 Emamectin benzoate 100‐998 KARATE 1EC 100 SYNGENTA CROP PROTECTION, LLC 13.1 lambda‐Cyhalothrin 100‐1075 FORCE 3G INSECTICIDE 100 SYNGENTA CROP PROTECTION, LLC 3 Tefluthrin Acetochlor; Carbamothioic acid, dipropyl‐ 100‐1083 DOUBLEPLAY SELECTIVE HERBICIDE 100 SYNGENTA CROP PROTECTION, LLC 16.9; 67.8 , S‐ethyl ester 100‐1086 KARATE EC‐W INSECTICIDE 100 SYNGENTA CROP PROTECTION, LLC 13.1 lambda‐Cyhalothrin 100‐1088 SCIMITAR GC INSECTICIDE 100 SYNGENTA CROP PROTECTION,
    [Show full text]
  • Cypermethrin
    International Environmental Health Criteria 82 Cypermethrin Published under the joint sponsorship of the United Nations Environment Programme, the International Labour Organisation, and the World Health Organization WORLD HEALTH ORGANIZATION GENEVA 1989 Other titles available in the ENVIRONMENTAL HEALTH CRITERIA series include: 1. Mercury 2. Polychlorinated Biphenyls and Terphenyls 3. Lead 4. Oxides of Nitrogen 5. Nitrates, Nitrites, and N-Nitroso Compounds 6. Principles and Methods for Evaluating the Toxicity of Chemicals, Part 1 7. Photochemical Oxidants 8. Sulfur Oxides and Suspended Particulate Matter 9. DDT and its Derivatives 10. Carbon Disulfide 11. Mycotoxins 12. Noise 13. Carbon Monoxide 14. Ultraviolet Radiation 15. Tin and Organotin Compounds 16. Radiofrequency and Microwaves 17. Manganese 18. Arsenic 19. Hydrogen Sulfide 20. Selected Petroleum Products 21. Chlorine and Hydrogen Chloride 22. Ultrasound 23. Lasers and Optical Radiation 24. Titanium 25. Selected Radionuclides 26. Styrene 27. Guidelines on Studies in Environmental Epidemiology 28. Acrylonitrile 29. 2,4-Dichlorophenoxyacetic Acid (2,4-D) 30. Principles for Evaluating Health Risks to Progeny Associated with Exposure to Chemicals during Pregnancy 31. Tetrachloroethylene 32. Methylene Chloride 33. Epichlorohydrin 34. Chlordane 35. Extremely Low Frequency (ELF) Fields 36. Fluorine and Fluorides 37. Aquatic (Marine and Freshwater) Biotoxins 38. Heptachlor 39. Paraquat and Diquat 40. Endosulfan 41. Quintozene 42. Tecnazene 43. Chlordecone 44. Mirex continued on p. 156
    [Show full text]
  • Insecticide Residue Analyses in Cucumbers Sampled from Çanakkale Open Markets1 Çanakkale Açık Pazarlarından Örneklenen Hıyarlarda Insektisit Kalıntı Analizleri
    Türk. entomol. derg., 2020, 44 (4): 449-460 ISSN 1010-6960 DOI: http://dx.doi.org/10.16970/entoted.767482 E-ISSN 2536-491X Original article (Orijinal araştırma) Insecticide residue analyses in cucumbers sampled from Çanakkale open markets1 Çanakkale açık pazarlarından örneklenen hıyarlarda insektisit kalıntı analizleri Hayriye ÇATAK2 Osman TİRYAKİ3* Abstract The aim of this study was to investigate four insecticide residues in cucumbers with the aid of QuEChERS 2007.1 method. For method verification assessment, pesticide-free cucumber matrix was spiked with 0.1, 1 and 10 times of MRL for each pesticide. The QuEChERS-LC-MS/MS analytical method revealed that the detection limits of the insecticides were below the MRLs and the overall recovery of method was 97.7%. These figures were within the SANTE recovery limits (60-140%) and the values specified for the repeatability (≤20%). Cucumbers were collected from six different stands (A-F) at Çanakkale open markets for 6 weeks between 23 November and 28 December 2018. Residues of each sampling time and each stand were assessed. Acetamiprid residue of 257g and 236 µg/kg were detected in week 5 from stand B and in week 2 from stand E, respectively. These values are close to MRL (300 µg/kg). Formetanate hydrochloride residue of the week 3 from stand F (36.3 µg/kg) was more than MRL of 10 µg/kg. Pirimiphos methyl and chlorpyrifos residues were not detected in cucumbers. Theoretical maximum daily intake assessment showed that there was no chronic exposure risk for these four pesticides through cucumber consumption. Keywords: Cucumber, insecticide residues, QuEChERS, risk assessment, toxicology Öz Bu çalışma hıyarlarda dört insektisit kalıntısını QuEChERS 2007.1 yöntemi ile belirlemek amacıyla yapılmıştır.
    [Show full text]
  • Monitoring of Pesticide Residues in Commonly Used Fruits and Vegetables in Kuwait
    International Journal of Environmental Research and Public Health Article Monitoring of Pesticide Residues in Commonly Used Fruits and Vegetables in Kuwait Mustapha F. A. Jallow *, Dawood G. Awadh, Mohammed S. Albaho, Vimala Y. Devi and Nisar Ahmad Environment and Life Sciences Research Center, Kuwait Institute for Scientific Research, P.O. Box 24885, Safat 13109, Kuwait; [email protected] (D.G.A.); [email protected] (M.S.A.); [email protected] (V.Y.D.); [email protected] (N.A.) * Correspondence: [email protected]; Tel.: +965-249-8984 Received: 1 May 2017; Accepted: 12 July 2017; Published: 25 July 2017 Abstract: The presence of pesticide residues in primary and derived agricultural products raises serious health concerns for consumers. The aim of this study was to assess the level of pesticide residues in commonly consumed fruits and vegetables in Kuwait. A total of 150 samples of different fresh vegetables and fruits were analyzed for the presence of 34 pesticides using the quick easy cheap effective rugged and safe (QuEChERS) multi-residue extraction, followed by gas chromatography-mass spectrometry (GC-MS) or liquid chromatography-tandem mass spectrometry (LC-MS/MS). Pesticide residues above the maximum residue limits (MRL) were detected in 21% of the samples and 79% of the samples had no residues of the pesticides surveyed or contained residues below the MRL. Multiple residues were present in 40% of the samples with two to four pesticides, and four samples were contaminated with more than four pesticide residues. Of the pesticides investigated, 16 were detected, of which imidacloprid, deltamethrin, cypermethrin, malathion, acetamiprid, monocrotophos, chlorpyrifos-methyl, and diazinon exceeded their MRLs.
    [Show full text]
  • (PAC) Rev 24 Based on Applicable Aegls, Erpgs, Or Teels (Chemicals Listed by CASRN) PAC Rev 24 – August 2008
    Table 3: Protective Action Criteria (PAC) Rev 24 based on applicable AEGLs, ERPGs, or TEELs (Chemicals listed By CASRN) PAC Rev 24 – August 2008 Table 3 presents a listing of chemicals and PAC data based on the Chemical Abstract Service Registry Numbers (CASRNs)1 of the chemicals. Chemicals without an identified CASRN number are issued an identification number, preceded by the letter “z,” for purposes of the PAC data set. The columns presented in Table 3 provide the following information: Heading Definition No. The ordered numbering of the chemicals as they appear in this listing by CASRN. Chemical Name The common name of the chemical. CASRN The Chemical Abstract Service Registry Number for this chemical. TEEL-0 This is the threshold concentration below which most people will experience no appreciable risk of health effects. This PAC is always based on TEEL-0 because AEGL-0 or ERPG-0 values do not exist. PAC-1 Based on the applicable AEGL-1, ERPG-1, or TEEL-1 value. PAC-2 Based on the applicable AEGL-2, ERPG-2, or TEEL-2 value. PAC-3 Based on the applicable AEGL-3, ERPG-3, or TEEL-3 value. Units The units for the PAC values (ppm or mg/m3). Additional information on the chemicals presented here is provided in PAC Tables 1, 2, and 4. Table 3, other PAC Tables, introductory/explanatory material (including a glossary of acronyms and abbreviations), definitions of PAC values, and alternative methods of displaying PAC information are available electronically at: http://www.hss.energy.gov/HealthSafety/WSHP/chem_safety/teel.html.
    [Show full text]
  • Transport of Dangerous Goods
    ST/SG/AC.10/1/Rev.16 (Vol.I) Recommendations on the TRANSPORT OF DANGEROUS GOODS Model Regulations Volume I Sixteenth revised edition UNITED NATIONS New York and Geneva, 2009 NOTE The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. ST/SG/AC.10/1/Rev.16 (Vol.I) Copyright © United Nations, 2009 All rights reserved. No part of this publication may, for sales purposes, be reproduced, stored in a retrieval system or transmitted in any form or by any means, electronic, electrostatic, magnetic tape, mechanical, photocopying or otherwise, without prior permission in writing from the United Nations. UNITED NATIONS Sales No. E.09.VIII.2 ISBN 978-92-1-139136-7 (complete set of two volumes) ISSN 1014-5753 Volumes I and II not to be sold separately FOREWORD The Recommendations on the Transport of Dangerous Goods are addressed to governments and to the international organizations concerned with safety in the transport of dangerous goods. The first version, prepared by the United Nations Economic and Social Council's Committee of Experts on the Transport of Dangerous Goods, was published in 1956 (ST/ECA/43-E/CN.2/170). In response to developments in technology and the changing needs of users, they have been regularly amended and updated at succeeding sessions of the Committee of Experts pursuant to Resolution 645 G (XXIII) of 26 April 1957 of the Economic and Social Council and subsequent resolutions.
    [Show full text]
  • Bufadienolides from the Skin Secretions of the Neotropical Toad Rhinella Alata (Anura: Bufonidae): Antiprotozoal Activity Against Trypanosoma Cruzi
    molecules Article Bufadienolides from the Skin Secretions of the Neotropical Toad Rhinella alata (Anura: Bufonidae): Antiprotozoal Activity against Trypanosoma cruzi Candelario Rodriguez 1,2,3 , Roberto Ibáñez 4 , Luis Mojica 5, Michelle Ng 6, Carmenza Spadafora 6 , Armando A. Durant-Archibold 1,3,* and Marcelino Gutiérrez 1,* 1 Centro de Biodiversidad y Descubrimiento de Drogas, Instituto de Investigaciones Científicas y Servicios de Alta Tecnología (INDICASAT AIP), Apartado 0843-01103, Panama; [email protected] 2 Department of Biotechnology, Acharya Nagarjuna University, Nagarjuna Nagar, Guntur 522510, India 3 Departamento de Bioquímica, Facultad de Ciencias Naturales, Exactas y Tecnología, Universidad de Panamá, Apartado 0824-03366, Panama 4 Smithsonian Tropical Research Institute (STRI), Balboa, Ancon P.O. Box 0843-03092, Panama; [email protected] 5 Centro Nacional de Metrología de Panamá (CENAMEP AIP), Apartado 0843-01353, Panama; [email protected] 6 Centro de Biología Celular y Molecular de Enfermedades, INDICASAT AIP, Apartado 0843-01103, Panama; [email protected] (M.N.); [email protected] (C.S.) * Correspondence: [email protected] (A.A.D.-A.); [email protected] (M.G.) Abstract: Toads in the family Bufonidae contain bufadienolides in their venom, which are charac- Citation: Rodriguez, C.; Ibáñez, R.; terized by their chemical diversity and high pharmacological potential. American trypanosomiasis Mojica, L.; Ng, M.; Spadafora, C.; is a neglected disease that affects an estimated 8 million people in tropical and subtropical coun- Durant-Archibold, A.A.; Gutiérrez, M. tries. In this research, we investigated the chemical composition and antitrypanosomal activity Bufadienolides from the Skin of toad venom from Rhinella alata collected in Panama.
    [Show full text]
  • Hazardous Substance Fact Sheet
    Right to Know Hazardous Substance Fact Sheet Common Name: DIOXOLANE Synonyms: 1,3-Dioxolan; Formal Glycol; Glycol Methylene Ether CAS Number: 646-06-0 Chemical Name: 1,3-Dioxolane RTK Substance Number: 0791 Date: February 1999 Revision: April 2008 DOT Number: UN 1166 Description and Use EMERGENCY RESPONDERS >>>> SEE BACK PAGE Dioxolane is a clear, colorless liquid with an Ether-like odor. It Hazard Summary is used in lithium batteries and as a solvent for oils, fats, waxes Hazard Rating NJDOH NFPA and dyes. HEALTH - 1 FLAMMABILITY - 3 REACTIVITY - 2 FLAMMABLE AND REACTIVE POISONOUS GASES ARE PRODUCED IN FIRE CONTAINERS MAY EXPLODE IN FIRE Hazard Rating Key: 0=minimal; 1=slight; 2=moderate; 3=serious; Reasons for Citation 4=severe f Dioxolane is on the Right to Know Hazardous Substance List because it is cited by ACGIH, DOT, and NFPA. f Dioxolane can affect you by ingestion and may be absorbed f This chemical is on the Special Health Hazard Substance through the skin. List. f Contact can irritate and burn the skin and eyes with possible eye damage. f Inhaling Dioxolane can irritate the nose and throat causing coughing and wheezing. f Exposure to Dioxolane may damage the nervous system. f Dioxolane may damage the kidneys. f Dioxolane is FLAMMABLE and REACTIVE and a SEE GLOSSARY ON PAGE 5. DANGEROUS FIRE and EXPLOSION HAZARD. FIRST AID Eye Contact f Immediately flush with large amounts of cool water for at Workplace Exposure Limits least 15 minutes, lifting upper and lower lids. Remove ACGIH: The threshold limit value (TLV) is 20 ppm averaged contact lenses, if worn, while flushing.
    [Show full text]
  • Preventive and Therapeutic Effects of Chinese Herbal Compounds Against Hepatocellular Carcinoma
    molecules Review Preventive and Therapeutic Effects of Chinese Herbal Compounds against Hepatocellular Carcinoma Bing Hu 1,*, Hong-Mei An 2, Shuang-Shuang Wang 1, Jin-Jun Chen 3 and Ling Xu 1 1 Department of Oncology and Institute of Traditional Chinese Medicine in Oncology, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200032, China; [email protected] (S.-S.W.); [email protected] (L.X.) 2 Department of Science & Technology, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 202032, China; [email protected] 3 Department of Plastic & Reconstructive Surgery, Shanghai Key Laboratory of Tissue Engineering, The Ninth People’s Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai 200011, China; [email protected] * Correspondence: [email protected]; Tel.: +86-21-64385700 Academic Editor: Derek J. McPhee Received: 16 November 2015 ; Accepted: 20 January 2016 ; Published: 27 January 2016 Abstract: Traditional Chinese Medicines, unique biomedical and pharmaceutical resources, have been widely used for hepatocellular carcinoma (HCC) prevention and treatment. Accumulated Chinese herb-derived compounds with significant anti-cancer effects against HCC have been identified. Chinese herbal compounds are effective in preventing carcinogenesis, inhibiting cell proliferation, arresting cell cycle, inducing apoptosis, autophagy, cell senescence and anoikis, inhibiting epithelial-mesenchymal transition, metastasis and angiogenesis, regulating immune function, reversing drug
    [Show full text]
  • Questions in the Chemical Enzymology of MAO
    Review Questions in the Chemical Enzymology of MAO Rona R. Ramsay 1,* and Alen Albreht 2 1 Biomedical Sciences Research Complex, School of Biology, University of St Andrews, St Andrews KY16 9ST, UK 2 Laboratory for Food Chemistry, Department of Analytical Chemistry, National Institute of Chemistry, Hajdrihova 19, SI-1000 Ljubljana, Slovenia; [email protected] * Correspondence: [email protected]; Tel.: +44-(0)-1334-474740 Abstract: We have structure, a wealth of kinetic data, thousands of chemical ligands and clinical information for the effects of a range of drugs on monoamine oxidase activity in vivo. We have comparative information from various species and mutations on kinetics and effects of inhibition. Nevertheless, there are what seem like simple questions still to be answered. This article presents a brief summary of existing experimental evidence the background and poses questions that remain intriguing for chemists and biochemists researching the chemical enzymology of and drug design for monoamine oxidases (FAD-containing EC 4.1.3.4). Keywords: chemical mechanism; kinetic mechanism; oxidation; protein flexibility; cysteine modifica- tion; reversible/irreversible inhibition; molecular dynamics; simulation 1. Introduction Monoamine oxidase (E.C. 1.4.3.4) enzymes MAO A and MAO B are FAD-containing Citation: Ramsay, R.R.; Albreht, A. proteins located on the outer face of the mitochondrial inner membrane, retained there Questions in the Chemical Enzymology of MAO. Chemistry 2021, by hydrophobic interactions and a transmembrane helix. The redox co-factor (FAD) is 3, 959–978. https://doi.org/10.3390/ covalently attached to a cysteine and buried deep inside the protein [1].
    [Show full text]
  • United Nations LAWS and REGULATIONS FRANCE
    E/NL.1950/9-16 1 March 1950 United Nations LAWS AND REGULATIONS PROMULGATED TO GIVE EFFECT TO THE PROVISIONS OF THE CONVENTION OF 13 JULY 1931 FOR LIMITING THE MANUFACTURE AND REGULATING THE DISTRIBUTION OF NARCOTIC DRUGS AS AMENDED BY THE PROTOCOL OF 11 DECEMBER 1946 FRANCE COMMUNICATED BY THE GOVERNMENT OF FRANCE Lake Success, New York, 1950 Note by the Secretary-General In accordance with Article 21 of the Convention of 13 July 1931 for Limiting the Manufacture and Regulating the Distribution of Narcotic Drugs, as amended by the Protocol of 11 December 1946, the Secretary-General has the honour to communicate here• after the texts of regulations. Ori gina1: English E/NL.1950/9 COMPOSITION OF PART II OF THE SCHEDULES OF POISONOUS SUBSTANCES* 1he Minister of Public Health and Population, •Considering the amended Act of 19 July 1845, Considering the Decree of 19 November 1943, and in particular Article 1 of the said Decree, Orders as follows: Article 1 The following substances shall be included in Schedule A, Part II: Arsenious oxide and arsenic acid Hydrocyanic acid Aconite (leaves, roots, extract and tincture) Aconitine and its salts Adrenaline Alkaloids of opium, their salts and their derivatives, other than those specifically mentioned in Schedule B Apomorphine and its salts Arecoline and its salts Arsenates and arsenites Metallic arsenic (cobalt) Atropine and its salts Belladonna (leaves, roots, powder and extract) Benzoate of mercury Dichloride of mercury Bi-iodide of mercury Bromo form Methyl bromide Brucine and its salts Cantharides (whole, powder and tincture) Cantharidin and its salts Chloroform Chloropicrin Hemlock (fruit, powder and extract) Codeine and its salts Colchicine and its salts Colchicum (seeds and extract) Conine and its salts Convalla toxin Indian berry The poisonous substances classified in the Codex without legal authority as "toxic" substances or as substances "to be kept separately" are not listed here.
    [Show full text]
  • Functional Evidence for Atypical Β-Adrenoceptors in Rat Isolated
    FUNCTIONAL EVIDENCE FOR ATYPICAL p-ADRENOCEPTORS IN RAT ISOLATED ARTERIES A thesis submitted by SONIA SOOCH for the degree of Doctor of Philosophy in the University of London. 1996 Department of Pharmacology University College London Gower Street London WCIE 6 BT ProQuest Number: 10055412 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a complete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. uest. ProQuest 10055412 Published by ProQuest LLC(2016). Copyright of the Dissertation is held by the Author. All rights reserved. This work is protected against unauthorized copying under Title 17, United States Code. Microform Edition © ProQuest LLC. ProQuest LLC 789 East Eisenhower Parkway P.O. Box 1346 Ann Arbor, Ml 48106-1346 Abstract Since the original classification by Lands et al (1967a), it has become evident that not all (3-adrenoceptor mediated responses can be classified as either (3i or P 2, with the existence of an additional p-adrenoceptor subtype, referred to as the atypical or p 3-adrenoceptor. This p-adrenoceptor subtype has been identified in adipose and gastrointestinal tissue, as well as skeletal muscle and airway smooth muscle. The work presented in this thesis demonstrates the presence of atypical p-adrenoceptors in rat vasculature. The present in vitro results show that relaxations to isoprenaline in the rat thoracic aorta, mesenteric and pulmonary artery, are antagonized by propranolol in a non-competitive manner.
    [Show full text]