Articles:
| None found yet. Try the PubMed Search. |
2-propenoic acid, 3-(3-hydroxyphenyl)-, (E)-
Notes:
Present in roots of Citrus sinensis (orange), Citrus limon (lemon) and Citrus paradisi (grapefruit)
Coumaric acid is a hydroxycinnamic acid, an organic compound that is a hydroxy derivative of cinnamic acid. There are three isomers, o-coumaric acid, m-coumaric acid, and p-coumaric acid, that differ by the position of the hydroxy substitution of the phenyl group. p-Coumaric acid is the most abundant isomer of the three in nature. (Wikipedia)
-
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): 14755-02-3 3-Hydroxycinnamic acid >95% 3-Hydroxycinnamic acid is found in the barks of Cinnamomum cassia Presl, it has antioxidant activity.
-
-
TCI AMERICA Moving Your Chemistry Forward We continuously strive to advance our technology. With East & West Coast distribution centers, count on TCI to deliver products quickly and reliably. Over 30,000 Reagents available today in benchtop to bulk quantities. We also offer custom synthesis solutions. Sign up for a TCI account today for fast and free shipping! Tokyo Chemical Industry Co., Ltd. (TCI) is a leading worldwide manufacturer of specialty organic chemicals founded in 1946. TCI provides organic laboratory chemicals as well as pharmaceutical, cosmetic and functional materials. More than 70 years of synthesis experience and multi-purpose plants enable TCI to offer more than 30,000 products as well as custom synthesis. US Email: Sales Email: Technical Support Voice: 1-800-423-8616 Fax: 1- 888-520-1075 Facebook Twitter Instagram Linkedin Product(s): C0655 trans-m-Coumaric Acid >99.0%(GC)(T)
-
| CAS Number: | 14755-02-3 |  3D/inchi
|
| Nikkaji Web: | J136.385I | |
| Beilstein Number: | 2084229 | |
| MDL: | MFCD00004390 | |
| XlogP3: | 1.80 (est) | |
| Molecular Weight: | 164.16036000 | |
| Formula: | C9 H8 O3 | |
| 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:
| Assay: | 95.00 to 100.00 % |
| Food Chemicals Codex Listed: | No |
| Boiling Point: | 373.00 to 374.00 °C. @ 760.00 mm Hg (est) |
| Vapor Pressure: | 0.000003 mmHg @ 25.00 °C. (est) |
| Flash Point: | 381.00 °F. TCC ( 193.70 °C. ) (est) |
| logP (o/w): | 1.826 (est) |
| Soluble in: | |
| alcohol | |
| water, 2.709e+004 mg/L @ 25 °C (est) | |
Organoleptic Properties:
| Odor and/or flavor descriptions from others (if found). | |
Cosmetic Information:
| None found |
Suppliers:
| Alfa Biotechnology |
| For experimental / research use only. |
| 3-Hydroxycinnamic acid 98% |
| BOC Sciences |
| For experimental / research use only. |
| 3-Hydroxycinnamic acid >95%
Odor: characteristic Use: 3-Hydroxycinnamic acid is found in the barks of Cinnamomum cassia Presl, it has antioxidant activity. |
| EMD Millipore |
| For experimental / research use only. |
| 3-Hydroxycinnamic acid |
| ExtraSynthese |
| For experimental / research use only. |
| 3-Coumaric acid (HPLC) ≥90% |
| Matrix Scientific |
| For experimental / research use only. |
| (2E)-3-(3-Hydroxyphenyl)acrylic acid |
| Santa Cruz Biotechnology |
| For experimental / research use only. |
| trans-3-Hydroxycinnamic acid 98% |
| Sigma-Aldrich: Aldrich |
| For experimental / research use only. |
| trans-3-Hydroxycinnamic acid 99% |
| TCI AMERICA |
| For experimental / research use only. |
| trans-m-Coumaric Acid >99.0%(GC)(T) |
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 (E)-meta-hydroxycinnamic acid usage levels up to: | |||
| not for fragrance use. | |||
| Recommendation for (E)-meta-hydroxycinnamic acid flavor usage levels up to: | |||
| not for flavor use. | |||
Safety References:
| EPI System: | View |
| AIDS Citations: | Search |
| Cancer Citations: | Search |
| Toxicology Citations: | Search |
| EPA ACToR: | Toxicology Data |
| EPA Substance Registry Services (SRS): | Registry |
| Laboratory Chemical Safety Summary : | 637541 |
| National Institute of Allergy and Infectious Diseases: | Data |
| WGK Germany: | 3 |
| (E)-3-(3-hydroxyphenyl)prop-2-enoic acid | |
| Chemidplus: | 0014755023 |
References:
| (E)-3-(3-hydroxyphenyl)prop-2-enoic acid | |
| NIST Chemistry WebBook: | Search Inchi |
| Pubchem (cid): | 637541 |
| Pubchem (sid): | 134976365 |
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 |
| Golm Metabolome Database: | Search |
| Metabolomics Database: | Search |
| KEGG (GenomeNet): | C12621 |
| HMDB (The Human Metabolome Database): | HMDB01713 |
| FooDB: | FDB002591 |
| Export Tariff Code: | 2918.29.2000 |
| VCF-Online: | VCF Volatile Compounds in Food |
| ChemSpider: | View |
Potential Blenders and core components note
| None Found | ||
Potential Uses:
| None Found |
Occurrence (nature, food, other): note
| cinnamon Search PMC Picture | |
| grapefruit root Search Trop Picture | |
| lemon root Search Trop Picture | |
| orange root Search Trop Picture |
Synonyms:
| (E)-3- | coumaric acid |
| (E)-m- | coumaric acid |
| (E)-meta- | coumaric acid |
| trans-3- | coumaric acid |
| trans-m- | coumaric acid |
| trans-meta- | coumaric acid |
| (E)-3- | hydroxycinnamic acid |
| (E)-m- | hydroxycinnamic acid |
| trans-3- | hydroxycinnamic acid |
| trans-m- | hydroxycinnamic acid |
| trans-meta- | hydroxycinnamic acid |
| 3- | hydroxycinnamic acid (predominantly trans) |
| (2E)-3-(3- | hydroxyphenyl)-2-propenoic acid |
| (E)-3-(3- | hydroxyphenyl)-2-propenoic acid |
| (2E)-3-(3- | hydroxyphenyl)acrylic acid |
| (E)-3-(3- | hydroxyphenyl)acrylic acid |
| (2E)-3-(3- | hydroxyphenyl)prop-2-enoic acid |
| (E)-3-(3- | hydroxyphenyl)prop-2-enoic acid |
| trans-3-(3- | hydroxyphenyl)prop-2-enoic acid |
| 2- | propenoic acid, 3-(3-hydroxyphenyl)-, (2E)- |
| 2- | propenoic acid, 3-(3-hydroxyphenyl)-, (E)- |