Articles:
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dicaffeoyl-L-tartaric acid
Notes:
Constit. of leaves of chicory (Cichorium intybus) and endive Cichorium endivia
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BOC Sciences Best of Chemicals Supplier Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds. BOC Sciences provides a wide range of services to support the pharmaceutical industry through all stages of drug discovery including Custom Synthesis of those chemicals that are not in stock, Isotope Labeling Service, Chiral Synthesis and Resolution, Bioconjugation, PEGylation services, analytical services. BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies. Email: Marketing US Email: Marketing Email: Sales US Email: Sales Voice: 1-631-485-4226 Fax: 1-631-614-7828 US Voice: 1-631-485-4226 US Fax: 1-631-614-7828 Europe 44-203-286-1088 Facebook Twitter Linkedin Blog Get the App! Product(s): 6537-80-0 (-)-laevo-Chicoric acid >98% antiviral
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Glentham Life Sciences Ltd The Chemical, Biochemical & Research Essentials Supplier Glentham Life Sciences is a supplier of fine chemicals and raw materials with warehousing, laboratories and packaging facilities in the UK. With a Glentham Life Sciences account you can view more product details, request quotes and order products online. Email: Info Email: Sales Email: Tech Support Voice: +44 (0) 1225 667798 Fax: +44 (0) 2033 978909 Facebook Twitter Linkedin Google+ News Distribution Products List: View Product(s): GL0945 Chicoric acid
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| CAS Number: | 6537-80-0 |  3D/inchi
|
| FDA UNII: | S4YY3V8YHD | |
| Nikkaji Web: | J431.736J | |
| MDL: | MFCD22683653 | |
| XlogP3-AA: | 2.00 (est) | |
| Molecular Weight: | 474.37586000 | |
| Formula: | C22 H18 O12 | |
| BioActivity Summary: | listing | |
| NMR Predictor: | Predict (works with chrome or firefox) | |
Category: natural substances and extractives
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
| Google Scholar: | Search |
| Google Books: | Search |
| Google Scholar: with word "volatile" | Search |
| Google Scholar: with word "flavor" | Search |
| Google Scholar: with word "odor" | Search |
| Google Patents: | Search |
| US Patents: | Search |
| EU Patents: | Search |
| Pubchem Patents: | Search |
| PubMed: | Search |
| NCBI: | Search |
Physical Properties:
| Appearance: | colorless needles (est) |
| Assay: | 95.00 to 100.00 % |
| Food Chemicals Codex Listed: | No |
| Boiling Point: | 784.00 to 786.00 °C. @ 760.00 mm Hg |
| Flash Point: | 523.00 °F. TCC ( 272.78 °C. ) |
| logP (o/w): | 3.090 (est) |
| Soluble in: | |
| alcohol | |
| water, slightly | |
| water, 25.62 mg/L @ 25 °C (est) | |
| Insoluble in: | |
| water | |
Organoleptic Properties:
| Odor and/or flavor descriptions from others (if found). | |
Cosmetic Information:
| None found |
Suppliers:
| Alfa Biotechnology |
| For experimental / research use only. |
| Cichoric acid 98% |
| BOC Sciences |
| For experimental / research use only. |
| (-)-laevo-Chicoric acid >98%
Odor: characteristic Use: antiviral |
| Dalton Pharma Services |
| For experimental / research use only. |
| Chicoric acid 98% |
| Glentham Life Sciences |
| Chicoric acid |
| Santa Cruz Biotechnology |
| For experimental / research use only. |
| Chicoric Acid ≥95% |
| Sigma-Aldrich: Sigma |
| For experimental / research use only. |
| Chicoric Acid ≥95% (HPLC) |
Safety Information:
| Preferred SDS: View | |
| Hazards identification | |
| Classification of the substance or mixture | |
| GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) | |
| None found. | |
| GHS Label elements, including precautionary statements | |
| Pictogram | |
| Hazard statement(s) | |
| None found. | |
| Precautionary statement(s) | |
| None found. | |
| Oral/Parenteral Toxicity: | |
| Not determined | |
| Dermal Toxicity: | |
| Not determined | |
| Inhalation Toxicity: | |
| Not determined | |
Safety in Use Information:
| Category: | natural substances and extractives | ||
| Recommendation for (-)-laevo-chicoric acid usage levels up to: | |||
| not for fragrance use. | |||
| Recommendation for (-)-laevo-chicoric acid flavor usage levels up to: | |||
| not for flavor use. | |||
Safety References:
| EPI System: | View |
| Cancer Citations: | Search |
| Toxicology Citations: | Search |
| EPA ACToR: | Toxicology Data |
| EPA Substance Registry Services (SRS): | Registry |
| Laboratory Chemical Safety Summary : | 5281764 |
| National Institute of Allergy and Infectious Diseases: | Data |
| WGK Germany: | 3 |
| (2R,3R)-2,3-bis[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy]butanedioic acid | |
| Chemidplus: | 0006537800 |
References:
| (2R,3R)-2,3-bis[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy]butanedioic acid | |
| NIST Chemistry WebBook: | Search Inchi |
| Pubchem (cid): | 5281764 |
| Pubchem (sid): | 135194152 |
Other Information:
| (IUPAC): | Atomic Weights of the Elements 2011 (pdf) |
| Videos: | The Periodic Table of Videos |
| tgsc: | Atomic Weights use for this web site |
| (IUPAC): | Periodic Table of the Elements |
| CHEBI: | View |
| CHEMBL: | View |
| KEGG (GenomeNet): | C10437 |
| HMDB (The Human Metabolome Database): | HMDB02375 |
| FooDB: | FDB002580 |
| VCF-Online: | VCF Volatile Compounds in Food |
| ChemSpider: | View |
| Wikipedia: | View |
Potential Blenders and core components note
| None Found | ||
Potential Uses:
| None Found |
Occurrence (nature, food, other): note
| chicory leaf Search Trop Picture | |
| dandelion Search Trop Picture | |
| endive Search Trop Picture | |
| lettuce Search Trop Picture |
Synonyms:
| butanedioic acid, 2,3-bis(((2E)-3-(3,4-dihydroxphenyl)-1-oxo-2-propenyl)oxy)-, (2R,3R)- | |
| butanedioic acid, 2,3-bis((3-(3,4-dihydroxphenyl)-1-oxo-2-propenyl)oxy)-, (R-(R*,R*-(E,E)))- | |
| butanedioic acid, 2,3-bis((3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl)oxy)-, (R-(R*,R*))- | |
| butanedioic acid, 2,3-bis[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-, (2R,3R)- | |
| butanedioic acid, 2,3-bis[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-, (2R,3R)- | |
| butanedioic acid, 2,3-bis[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-, (2R,3R)- (9CI) | |
| butanedioic acid, 2,3-bis[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-, [R-[R*,R*-(E,E)]]- | |
| (-)- | chicoric acid |
| (-)-L- | chicoric acid |
| L- | chicoric acid |
| chicoric acid, (-)- | |
| dicaffeoyl-L-tartaric acid | |
| dicaffeoyl-laevo-tartaric acid | |
| (R-(R*,R*-(E,E)))-2,3-bis((3-(3,4- | dihydroxphenyl)-1-oxo-2-propenyl)oxy)butanedioic acid |
| (2R,3R)-2,3-bis-[(E)-3-(3,4- | dihydroxy-phenyl)-acryloyloxy]-succinic acid |
| 2,3-bis((3-(3,4- | dihydroxyphenyl)-1-oxo-2-propenyl)oxy)butanedioic acid |
| (2R,3R)-2,3-bis[[(E)-3-(3,4- | dihydroxyphenyl)prop-2-enoyl]oxy]butanedioic acid |
| (2R,3R)-2,3-bis{[(2E)-3-(3,4- | dihydroxyphenyl)prop-2-enoyl]oxy}butanedioic acid |
| (2R,3R)-2,3-bis{[(2E)-3-(3,4- | dihydroxyphenyl)prop-2-enoyl]oxy}succinic acid |