Ingredient Guide
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
(12) United States Patent (10) Patent No.: US 9,168,397 B2 Amalric Et Al
US009 168397B2 (12) United States Patent (10) Patent No.: US 9,168,397 B2 Amalric et al. (45) Date of Patent: Oct. 27, 2015 (54) POWDERY EMULSIFYING COMPOSITION A61Q 19/005; A61Q 1/02: A61K 8/92: OF ALKYL POLYGLYCOSIDES, USE A61K 8/34: A61K 8/602: A61K 8/022: THEREOF FOR PREPARING COSMETC A61K 8/60; A61K 8/062: A61K 8/604; EMULSIONS, AND METHOD FOR A61K 8/06; A61K 8/342: A61K 2800/412: PREPARING SAME BO1F17/0092 See application file for complete search history. (71) Applicant: SOCIETE DEXPLOITATION DE PRODUITS POUR LES INDUSTRIES CHIMIQUES SEPPIC, (56) References Cited Paris (FR) U.S. PATENT DOCUMENTS (72) Inventors: Chantal Amalric, Blan (FR); Alicia Roso, Saix (FR); Agnes Gorce, 5,670471 A 9, 1997 Amalric et al. 5,888,482 A 3, 1999 Amalric et al. Marseille (FR) 5,958,431 A 9/1999 Brancq et al. 6,245,821 B1 6/2001 Bulcourt et al. (73) Assignee: SOCIETE DEXPLOITATION DE 6,268.400 B1 7/2001 Amalric et al. PRODUITS POUR LES 6,353,034 B1 3/2002 Amalric et al. INDUSTRIES CHIMIQUES SEPPIC, 6,488,946 B1 12/2002 Milius et al. Paris (FR) 6,723,774 B2 4/2004 Guntherberg et al. 2003/0105169 A1 6/2003 Lennon (*) Notice: Subject to any disclaimer, the term of this patent is extended or adjusted under 35 FOREIGN PATENT DOCUMENTS U.S.C. 154(b) by 0 days. EP O992508 4/2000 FR 2756195 5, 1998 (21) Appl. No.: 14/278,908 FR 2784904 4/2000 FR 283O464 4/2003 (22) Filed: May 15, 2014 WO 92O6778 4f1992 WO 9513863 5, 1995 (65) Prior Publication Data WO 9637285 11 1996 WO 9637286 11, 1996 US 2014/O2554.57 A1 Sep. -
( 12 ) United States Patent ( 10 ) Patent No .: US 10,751,310 B2 Freeman Et Al
US010751310B2 ( 12 ) United States Patent ( 10 ) Patent No .: US 10,751,310 B2 Freeman et al . ( 45 ) Date of Patent : Aug. 25 , 2020 ( 54 ) PREVENTION , TREATMENT AND ( 56 ) References Cited REVERSAL OF DISEASE USING THERAPEUTICALLY EFFECTIVE U.S. PATENT DOCUMENTS AMOUNTS OF DICARBOXYLIC ACID 3,527,789 A 9/1970 Payne COMPOUNDS 4,166,913 A 9/1979 Kesling , Jr. et al . 6,528,499 B1 * 3/2003 Kozikowski C07C 59/347 ( 71 ) Applicant: UNIVERSITY OF 514/574 8,324,277 B2 12/2012 Freeman PITTSBURGH — OF THE 8,735,449 B2 5/2014 Freeman COMMONWEALTH SYSTEM OF 9,066,902 B2 6/2015 Freeman et al . HIGHER EDUCATION , Pittsburgh , 9,186,408 B2 11/2015 Freeman et al . PA (US ) 9,700,534 B2 7/2017 Freeman et al . 9,750,725 B2 9/2017 Freeman et al . 10,213,417 B2 2/2019 Freeman et al . ( 72 ) Inventors : Bruce A. Freeman , Pittsburgh , PA 10,258,589 B2 4/2019 Freeman et al . ( US ) ; Francisco J. Schopfer , 2015/0018417 Al 1/2015 Freeman et al . Pittsburgh , PA ( US ) FOREIGN PATENT DOCUMENTS ( 73 ) Assignee : University of Pittsburgh — of the CN 103705499 4/2014 Commonwealth System of Higher DE 102011118462 5/2013 Education , Pittsburgh , PA ( US ) GB 1153464 5/1969 WO WO 2002/022627 3/2002 WO WO 2009/017802 2/2009 ( * ) Notice : Subject to any disclaimer , the term of this WO WO 2009/112455 9/2009 patent is extended or adjusted under 35 WO WO 2010/005521 1/2010 U.S.C. 154 ( b ) by 0 days . WO WO 2010/014889 2/2010 WO WO 2011/014261 2/2011 WO WO 2013/116753 8/2013 ( 21 ) Appl. -
C3gc42589d1.Pdf
Electronic Supplementary Material (ESI) for Green Chemistry. This journal is © The Royal Society of Chemistry 2014 Supporting Information Highly Efficient, NiAu-catalyzed Hydrogenolysis of Lignin into Phenolic Chemicals Jiaguang Zhang, Hiroyuki Asakura, Jeaphianne van Rijn, Jun Yang, Paul Duchesne, Bin Zhang, Xi Chen, Peng Zhang, Mark Saeys* and Ning Yan* Contents 1 Materials ............................................................................................................................................. 3 2 Synthesis of substrates ....................................................................................................................... 3 2.1 Organosolv Lignin ......................................................................................................................... 3 2.2 2‐phenoxy‐1‐phenethanol ........................................................................................................... 3 2.3 2‐(2‐methoxyphenyl)oxy‐1‐phenethanol ..................................................................................... 4 2.4 2‐(2,6‐dimethoxyphenyl)oxy‐1‐phenethanol ............................................................................... 4 2.5 1‐benzyloxy‐2‐methoxybenzene .................................................................................................. 4 3 Catalyst preparation and reaction ...................................................................................................... 4 3.1 Catalyst preparation .................................................................................................................... -
US Patent 4956170
United States Patent (19) 11 Patent Number: 4,956,170 Lee 45) Date of Patent: Sep. 11, 1990 (54. SKIN MOISTURIZING/CONDITIONING ter-Soluble Resins', B. F. Goodrich, Cleveland, Ohio, ANTMCROBAL. ALCOHOLC GELS pp. 15-16, 22-24, 27-28. Ultracol TM, A 70% Ethyl Alcohol Gel with Emol 75) Inventor: Andrew S. Lee, Racine, Wis. lients, Dexide, Inc., Ft. Worth, Tex., Package Label, 2 73 Assignee: S. C. Johnson & Son, Inc., Racine, pages. Wis. Advertisement, "Alpha 9 Instant Hand Sanitizer”, JDS 21 Appl. No.: 372,723 Mfg. Co., Hollywood, Calif., from Modern Salon, Aug. 1989, 1 page. 22 Filed: Jun. 28, 1989 51 int. Cl’................................................ A61K 7/06 Primary Examiner-Merrell C. Cashion, Jr. 52 U.S. C. ...................................... 424/81: 514/873; Assistant Examiner-E. J. Webman 514/944; 252/315.4 58 Field of Search .................. 424/81; 514/873,944; 57 ABSTRACT 523/105; 252/315.4 This invention relates to a high alcohol content antimi 56) References Cited crobial gel composition for frequent use in disinfecting the hands which possesses moisturizing and condition U.S. PATENT DOCUMENTS ing agents to counter the drying effects of the alcohol 2,054,989 9/1936 Moore................................... 167/58 on the skin in manner similar to that provides by hand 3,215,603 11/1965 Gross et al. ........................... 424/71 and body lotions. The gel compositions comprises from 3,427,382 2/1969 Haefele ................................. 424/7 3,485,915 12/1969 Gerstein et al. ...................... 424/81 about 60-75% ethanol; about 0.42% of a thickening 3,609,102 9/1971 Schlossman ........................ -
Redalyc.Degradation of Citronellol, Citronellal and Citronellyl Acetate By
Electronic Journal of Biotechnology E-ISSN: 0717-3458 [email protected] Pontificia Universidad Católica de Valparaíso Chile Tozoni, Daniela; Zacaria, Jucimar; Vanderlinde, Regina; Longaray Delamare, Ana Paula; Echeverrigaray, Sergio Degradation of citronellol, citronellal and citronellyl acetate by Pseudomonas mendocina IBPse 105 Electronic Journal of Biotechnology, vol. 13, núm. 2, marzo, 2010, pp. 1-7 Pontificia Universidad Católica de Valparaíso Valparaíso, Chile Available in: http://www.redalyc.org/articulo.oa?id=173313806002 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Electronic Journal of Biotechnology ISSN: 0717-3458 Vol.13 No.2, Issue of March 15, 2010 © 2010 by Pontificia Universidad Católica de Valparaíso -- Chile Received April 24, 2009 / Accepted November 6, 2009 DOI: 10.2225/vol13-issue2-fulltext-8 RESEARCH ARTICLE Degradation of citronellol, citronellal and citronellyl acetate by Pseudomonas mendocina IBPse 105 Daniela Tozoni Instituto de Biotecnologia Universidade de Caxias do Sul R. Francisco G. Vargas 1130 Caxias do Sul, RS, Brazil Jucimar Zacaria Instituto de Biotecnologia Universidade de Caxias do Sul R. Francisco G. Vargas 1130 Caxias do Sul, RS, Brazil Regina Vanderlinde Instituto de Biotecnologia Universidade de Caxias do Sul R. Francisco G. Vargas 1130 Caxias do Sul, RS, Brazil Ana Paula Longaray Delamare Universidade de Caxias do Sul R. Francisco G. Vargas 1130 Caxias do Sul, RS, Brazil Sergio Echeverrigaray* Universidade de Caxias do Sul R. Francisco G. Vargas 1130 Caxias do Sul, RS, Brazil E-mail: [email protected] Financial support: COREDES/FAPERGS, and D. -
ISOLATION of GERANIOL from RHODINOL by USING PDC REAGENT Nahso3 and Nabh4
The 2nd International Conference on Chemical Sciences Proceeding ISSN NO. 1410-8313 Yogyakarta, October 14-16th, 2010 ISOLATION OF GERANIOL FROM RHODINOL BY USING PDC REAGENT NaHSO3 AND NaBH4 Zaina Mukhia Bintan, Priatmoko1,*), and Hardono Sastrohamidjojo*) 1 Department of Chemistry, Universitas Gadjah Mada, Yogyakarta, Indonesia * Corresponding author, tel/fax : +62274545188 ABSTRACT Isolation geraniol from the rhodinol have been coducted by using PDC (pyridinium dichromate) reagent, NaHSO3 and NaBH4. The prosses consits of four steps : first step was rhodinol to get the high grade (it are compare between citronella oil from sample A, sample B and sample C, second step was the oxidation of rhodinol by using PDC, third step was separation of citral from citronellol by using sodium bisulfit, and the last step was reduction of citral to geraiol by using NaBH4 in etanol. The higher grade rhodinol was isolated from citronella oil of sample with purity 29.03%. The rhodinol wich used in this research was product of the third fraction redistillation of distillate the second fraction citronella oil, with grade of rhodinol was 90.55%. The oxidation of rhodinol by using PDC, could selectively oxidize geraniol become citral, whereas nothing change with citronellol. The product of oxidation was mixture of citral and citronellol, yellow liquid with fragnance odor, weight : 0.8 g. The geraniol can be obtained from reduction geraniol by using NaBH4 in ethanol. Product of reduction was colourless liquid, with fragnance odor, weight : 0.4 g. The product was analyzed by using GC and infrared spectrometer. Keywords: geraniol, citral, pyridinium dichromate INTRODUCTION Schmidts (1979 have also made the reagent to oxidase alcohol (primary, secondary and so he essential oil is a natural product that on) become the carbonyl compound. -
Organic Synthesis Using Clay and Clay-Supported Catalysts.Pdf
Applied Clay Science 53 (2011) 106–138 Contents lists available at ScienceDirect Applied Clay Science journal homepage: www.elsevier.com/locate/clay Review Article Organic synthesis using clay and clay-supported catalysts Gopalpur Nagendrappa ⁎,1 Department of Chemistry, Bangalore University, Bangalore 560 001, India article info abstract Article history: Clays and modified clays are used to catalyze various types of organic reactions such as addition, Michael Received 20 May 2010 addition, carbene addition and insertion, hydrogenation, allylation, alkylation, acylation, pericyclic reactions, Received in revised form 17 October 2010 condensation reactions, aldol formation, imine synthesis, diazotization reactions, synthesis of heterocycles, Accepted 19 October 2010 esterification reactions, rearrangement/isomerization reactions, cyclization reactions, oxidation of alcohols, Available online 6 October 2010 dehydrogenation, epoxidation and several more. Clays function as Brønsted and/or Lewis acids, or as bases. Clays with combined acidic and basic properties have been developed by simple procedures of modification. Keywords: Clay mineral Such clays are employed to catalyze a sequence of acid and base-catalyzed reactions in one pot. Good Activated bentonite enantioselectivity and stereoselectivity are achieved using chiral organic compounds and chiral complexes Montmorillonite intercalated between clay layers. Examples from recent literature are described here. Saponite © 2010 Elsevier B.V. All rights reserved. Organic synthesis Heterogeneous catalyst 1. Introduction compatibility and cheapness, much effort is expended in discovering newer methods of using clays in their native and modified forms as Clays are widespread, easily available and low-cost chemical catalysts for diverse organic reactions. substances. Both in their native state and in numerous modified Clays have a long history of use as catalysts and as supports in organic forms, clays are versatile materials that catalyze a variety of chemical reactions (Vogels et al., 2005). -
European Patent Office of Opposition to That Patent, in Accordance with the Implementing Regulations
(19) TZZ __T (11) EP 2 416 766 B1 (12) EUROPEAN PATENT SPECIFICATION (45) Date of publication and mention (51) Int Cl.: of the grant of the patent: A61K 31/045 (2006.01) A61K 45/06 (2006.01) 09.04.2014 Bulletin 2014/15 A61K 8/34 (2006.01) A61P 17/00 (2006.01) A61P 17/16 (2006.01) A61Q 19/00 (2006.01) (2006.01) (2006.01) (21) Application number: 09701247.0 A23L 1/30 A23L 2/02 A23L 2/39 (2006.01) A23C 9/13 (2006.01) A23C 11/10 (2006.01) A61Q 5/02 (2006.01) (22) Date of filing: 09.04.2009 A61Q 11/00 (2006.01) A61Q 15/00 (2006.01) A61Q 17/04 (2006.01) A61Q 19/02 (2006.01) A61K 8/02 (2006.01) A61Q 19/04 (2006.01) (86) International application number: PCT/EP2009/054336 (87) International publication number: WO 2009/087242 (16.07.2009 Gazette 2009/29) (54) COMPOSITIONS COMPRISING TRANS-TERT-BUTYL CYCLOHEXANOL AS SKIN IRRITATION- REDUCING AGENT ZUSAMMENSETZUNGEN MIT TRANS-TERT-BUTYL-CYCLOHEXANOL ALS MITTEL ZUR REDUZIERUNG VON HAUTREIZUNGEN COMPOSITIONS COMPRENANT DU TRANS-TERT-BUTYL CYCLOHEXANOL EN TANT QU’AGENT RÉDUISANT L’IRRITATION CUTANÉE (84) Designated Contracting States: • KROHN, Michael AT BE BG CH CY CZ DE DK EE ES FI FR GB GR 64653 Lorsch (DE) HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL • ZINKE, Holger PT RO SE SI SK TR 64646 Heppenheim (DE) (43) Date of publication of application: (74) Representative: Eisenführ Speiser 15.02.2012 Bulletin 2012/07 Patentanwälte Rechtsanwälte PartGmbB Postfach 10 60 78 (73) Proprietor: Symrise AG 28060 Bremen (DE) 37603 Holzminden (DE) (56) References cited: (72) Inventors: EP-A2- 0 755 910 WO-A1-97/22332 • VIELHABER, Gabriele WO-A1-2008/117254 US-A- 2 927 127 75008 Paris (FR) • OERTLING, Heiko • SYMRISE GMBH & CO KG ET AL: "Trans-tert- 1012 Lausanne (CH) butyl cyclohexanol as skin irritation-reducing • GÖMANN, Claudia agent" RESEARCH DISCLOSURE, MASON 37640 Warbsen (DE) PUBLICATIONS, HAMPSHIRE, GB, vol. -
Literature Digest, March 2018
Joseph Samec Research Group Digest Digest March 2018 Joseph Samec Research Group Digest Silver(I)‐Catalyzed Widely Applicable Aerobic 1,2‐Diol Oxidative Cleavage Dr. Zhong‐zhen Zhou Dr. Mingxin Liu Dr. Leiyang Lv Prof. Dr. Chao‐Jun Li Angew. Chem. Int. Ed. 2018, 57(10), 2616-2620 Abstract The oxidative cleavage of 1,2‐diols is a fundamental organic transformation. The stoichiometric oxidants that are still predominantly used for such oxidative cleavage, such as H5IO6 , Pb(OAc)4 , and KMnO4 , generate stoichiometric hazardous waste. Herein, we describe a widely applicable and highly selective silver(I)‐catalyzed oxidative cleavage of 1,2‐diols that consumes atmospheric oxygen as the sole oxidant, thus serving as a potentially greener alternative to the classical transformations. Solvent‐Free Enzyme Activity: Quick, High‐Yielding Mechanoenzymatic Hydrolysis of Cellulose into Glucose Dr. Fabien Hammerer Dr. Leigh Loots Jean‐Louis Do J. P. Daniel Therien Christopher W. Nickels Prof. Tomislav Friščić Prof. Dr. Karine Auclair Angew. Chem. Int. Ed. 2018, 57(10), 2621-2624 Abstract Mechanochemistry enables enzymatic cleavage of cellulose into glucose without bulk solvents, acids, other aggressive reagents, or substrate pre‐treatment. This clean mechanoenzymatic process (coined RAging) is also directly applicable to biomass, avoids many limitations associated with the use of cellulases, and produces glucose concentrations greater than three times that obtained by conventional methods. Joseph Samec Research Group Digest Synergistic N‐Heterocyclic Carbene/Palladium‐Catalyzed Reactions of Aldehyde Acyl Anions with either Diarylmethyl or Allylic Carbonates Dr. Shigeo Yasuda Takuya Ishii Shunsuke Takemoto Hiroki Haruki Prof. Dr. Hirohisa Ohmiya Angew. Chem. Int. Ed. -
UNITED STATES PATENT OFFICE 2,509,174 PROCESS of WATERPROOF NG TEXT LE Fabrics Milton J
Patented May 23, 1950 2,509,174 UNITED STATES PATENT OFFICE 2,509,174 PROCESS OF WATERPROOF NG TEXT LE FABRICs Milton J. Scott and Stuart H. Rider, Springfield, Mass, assignors to Monsanto Chemical Com pany, St. Louis, Mo., a corporation of Dela No Drawing. Application May 22, 1947, Serial No. 49,880 10 Claims. (C. 117-161) This invention relates to waterproofing con melamine containing about 2 mols of stearyl al positions and to materials treated therewith. cohol per mol of hexamethylol melamine. More particularly, the invention relates to cer tain aminotriazine-aldehyde-alcohol reaction Ecample I products and to cellulosic and proteinaceous ma 314 parts of spray dried crystalline hexa terials treated therewith. methylol melamine of Example I were mixed An object of this invention is to prepare water with 320 parts (10 mols) of anhydrous methanol proofing compositions. and 0.5 part of ethyl phosphoric acid. The mix A further object is to prepare aqueous emul ture was refluxed for 30 minutes at atmospheric sions of aminotriazine-aldehyde-alcohol reaction O pressure and then 404 (1.5 mols) parts of stearyl products. alcohol were added and refluxing continued for Another object is to provide waterproof coat 30 minutes. The solution was concentrated by S. vacuum distillation at about 25 inches of mercury Still another object is to provide Waterproof until the temperature rose to about 130 C. The textiles. S resulting material was a methyl stearyl ether of These and other objects are attained by pre hexamethylol melamine containing about 1.5 paring a liquid reaction product of an amino mols of stearyl alcohol per mol of hexamethylol triazine, an aldehyde, and two alcohols one of melamine. -
EDTA, Tetrasodium Tetrahydrate Salt
EDTA, Tetrasodium Tetrahydrate Salt sc-204735 Material Safety Data Sheet Hazard Alert Code Key: EXTREME HIGH MODERATE LOW Section 1 - CHEMICAL PRODUCT AND COMPANY IDENTIFICATION PRODUCT NAME EDTA, Tetrasodium Tetrahydrate Salt STATEMENT OF HAZARDOUS NATURE CONSIDERED A HAZARDOUS SUBSTANCE ACCORDING TO OSHA 29 CFR 1910.1200. NFPA FLAMMABILITY1 HEALTH3 HAZARD INSTABILITY0 SUPPLIER Company: Santa Cruz Biotechnology, Inc. Address: 2145 Delaware Ave Santa Cruz, CA 95060 Telephone: 800.457.3801 or 831.457.3800 Emergency Tel: CHEMWATCH: From within the US and Canada: 877-715-9305 Emergency Tel: From outside the US and Canada: +800 2436 2255 (1-800-CHEMCALL) or call +613 9573 3112 PRODUCT USE Chelating/sequestering agent for the clarification of liquids, pharmaceuticals, detergents, shampoos, agent for metal poisoning, decontamination of radioactive liquids and in analytical chemistry. Used in agricultural chemical sprays; metal cleaning and plating; to remove insoluble deposits of magnesium and calcium salts; in textiles to improve dying; scouring and detergent operations; decreasing blood cholesterol. SYNONYMS C10-H12-N2-Na4-O8, (OOCCH2)2NCH2CH2CH2N(CH2COO).Na4, "Tetracemate tetrasodium", "Versene 220", Aquamollin, "Edathanil tetrasodium", Tetracemin, Sequestrene, Complexon, Tyclarosol, "Endrate tetrasodium", Tetrine, Irrgalon, "Nervanaid B", Questex, Kalex, Calsol, Warkeelate, "edate terasodium", "Trilon B", Nervanoid, Aquamoline, "tetrasodium EDTA", Komplexon, "Syntes 12a", "tetrasodium edetate", Nullapon, Chemcolox, Conigon, ethylenebis(imminodiacetate), -
7 EDTA, Tetraso
REPORT Safety Assessment of EDTA, Calcium Disodium EDTA. Diammonium EDTA, Dipotassium EDTA. 7 Disodium EDTA, TEA- EDTA, Tetrasod=um EDTA, Tripotassium EDTA, Trisodium EDTA, HEDTA and Trisodium HEDTA ABSTRACT EDTA (ethylenediamine tetraacetic acid) and its salts are substituted diamines. HEDTA (hydroxyethyl ethylenediamine triacetic acid) and its trisodium salt are substituted amines. These ingredients function as chelating agents in cosmetic formulations. The typical concentration of use of EDTA is less than 2%, with the other salts in current use at even lower concentrations. The lowest dose reported to cause a toxic effect in animals was 750 mg/kg/day. These chelating agents are cytotoxic and weakly genotoxic, but not carcinogenic. Oral exposures to EDTA produced adverse reproductive and developmental effects in animals. Clinical tests reported no absorption of an EDTA salt through the skin. These ingredients, are likely, however, to affect the passage of other chemicals into the skin because they will chelate calcium. Exposure to ED TA in most cosmetic formulations, therefore, would produce systemic exposure levels well below those seen to be toxic in oral dosing studies. Exposure to EDTA in cosmetic formulations that may be inhaled, however, was a concern. An exposure assessment done using conservative assumptions predicted that the maximum EDTA dose via inhalation of an aerosolized cosmetic formulation is below that which has been shown to produce reproductive or developmental toxicity. Because of the potential to increase the penetration of other chemicals, formulators should continue to be aware of this when combining these ingredients with ingredients that previously have been determined to be safe primarily because they were not significanUy absorbed.