You can also browse global suppliers,vendor,prices,Price,manufacturers of trans-Cinnamic acid(140-10-3). Incompatible with strong oxidizing agents. MDL number MFCD00004369. ACM352431482. Molecular Weight 148.16 . It is involved in the production of methyl, ethyl and benzyl esters, which is used in the perfume industry. trans-cinnamic acid shows moderate inhibition on the rainbow trout intestinal isolates A. sobria SY-AS3 and S. baltica, SY-S145, gill isolate F. spartansii SY-FS1 and fish pathogens A. salmonicida ATCC 33658, Listonella anguillarum, SY-L24, V. crassostreae SY … Cinnamic acid, Pharmaceutical Secondary Standard; Certified Reference Material, certified reference material, pharmaceutical secondary standard, pkg of 200 mg, 1133933: Cinnamic acid, United States Pharmacopeia (USP) Reference Standard, 8.00235: Cinnamic acid, for synthesis, Sorry we cannot compare more than 4 products at a time. : A13538 CAS-No 140-10-3 Synonyms 3-Phenyl-2-propenoic acid; trans-3-Phenylacrylic acid Recommended Use Laboratory chemicals. The alkali salts are sol in water. Cinnamic acid. [1]. One such malignancy that still remains a therapeutic challenge mainly due to its heterogeneity and inaccessibility to t … L'acide cinnamique de formule C 6 H 5 –CH=CHCOOH est un acide organique qui se présente sous la forme d'une poudre blanche inodore, avec une faible solubilité dans l'eau. Phenylacrylic acid; 3-Phenylacrylic acid; 3-Phenyl-2-propenoic acid, 2916399090 other aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%, 4-09-00-02002 (Beilstein Handbook Reference). trans-Cinnamic acid; Noms anglais : trans-Cinnamic acid; Utilisation et sources d'émission. Home; Text Search; Structure Search ; About; GO. Viability is determined by Trypan-blue exclusion assay[1]. Mise à jour : 1984-01-30. trans-cinnamic acid: ChEBI ID CHEBI:35697: ChEBI ASCII Name trans-cinnamic acid: Definition The E (trans) isomer of cinnamic acid: Stars This entity has been manually annotated by the ChEBI Team. Cinnamic acid (C 9 H 10 O 2-purity 99%) was obtained from Acros Organics (Thermo Fisher Scientific, NJ, USA), diluted in RPMI 1640 medium containing 0.1 g/L of L-glutamine, 2.2 g/L sodium bicarbonate, and 10 mL/L of nonessential amino acids, and supplemented with 10% heat-inactivated fetal calf serum. Molecular Formula C 9 H 8 O 2; Average mass 148.159 Da; Monoisotopic mass 148.052429 Da; ChemSpider ID 392447 Molecular Formula: C 9 H 8 O 2; Molecular Weight: 148.161 g/mol; Cas Number: 140-10-3 ; EINECS Number: 205-398-1; MDL Number: MFCD00004369 ; InChIKey: WBYWAXJHAXSJNI … Date s: Modify: 2020-10-10. It serves as a precursor to the sweetener aspartame through enzyme-catalyzed amination to phenylalanine. Freely sol in benzene, ether, acetone, glacial acetic acid, carbon disulfide, oils. Liu L, et al. EC Number 205-398-1. CAS Number: 621-82-9; FEMA Number: 2288; Synonyms/Related: (2E)-3-phenylprop … It serves as a precursor to the sweetener aspartame through enzyme-catalyzed amination to phenylalanine. Service & Support. Il a été découvert et purifié par Péligot et Dumas en 1834. cinnamic acid. serum. Synonyms: TRANS-CINNAMIC-D5 ACID. - Find MSDS or SDS, a COA, data sheets and more information. Cinnamic acid; 2-Propenoic acid, 3-phenyl- (E)-; trans-3-Phenylacrylic acid; trans-beta-Carboxystyrene Chemical Name: trans-Cinnamic Acid Chemical Formula: C9-H8-O2 Contact Information: Sciencelab.com, Inc. 14025 Smith Rd. Environmental, Chemistry & Hazardous Materials News, Careers & Resources. CINNAMIC ACID U14A832J8D Overview Structure Names 25: Classification 2: Identifiers 12: Relationships 4: Metabolites 1: Active Moiety 1: Notes 3: Audit Info References 34: History 1: … Cinnamic acid - cas 140-10-3, synthesis, structure, density, melting point, boiling point. trans-Cinnamic acid is used in flavors, synthetic indigo and pharmaceuticals. Get Latest Price Request a quote. It is involved in the production of methyl, ethyl and benzyl esters, which is used in the perfume industry. At last,trans-Cinnamic acid… IndiaMART > Industrial Chemicals & Supplies > Cinnamic Acid. trans-Cinnamic acid is used in flavors, synthetic indigo and pharmaceuticals. Articles of Cinnamic acid are included as well. Hazard Symbols: Xi - Irritant: Risk Codes: R36/37/38 - Irritating to eyes, respiratory system and skin. Cinnamic acid, ethanol and temperature interaction on coumarate decarboxylase activity and the relative expression of the putative cd gene in D. bruxellensis Molecular Weight: 153.19 g/mol. Cinnamic acid is an organic compound with the formula C6H5CH=CHCOOH. B. Buying Leads | Details of the supplier of the safety data … The cell lines used, established from human malignant tumors, are A549 (lung cancer); PC3(M), Du145, and LNCaP (prostate cancer); A172, U251 (glioblastoma); and SKMEL28, A375(M), 1011 (melanoma). It is found in Cinnamomum cassia. CAS 140-10-3, chemical formula C₆H₅CH=CHCOOH. Cinnamic acid; Utilisation et sources d'émission. Cinnamic acid: a natural product with potential use in cancer intervention. ethyl 4-imino-2-oxo-1,2,3,4-tetrahydro-5-pyrimidinecarboxylate, 1-phenyl-3,4-dihydro[1]benzothieno[3,2-c]pyridine, 1,2-diphenyl-2-(2-pyridinylamino)ethanone (20622-21-3), methyl 2-[(1Z)-2-nitro-1-propenyl]phenyl ether (6306-34-9), N,N-dimethyl-1-phenyl-1-propanamine (3330-05-0), 6-(4-chlorophenyl)-4,5-dihydro-3(2H)-pyridazinone (1079-73-8), 4,4'-Diaminodicyclohexylmethane (1761-71-3), ethyl 1-ethyl-4-(4-hydroxyphenyl)-2-oxo-3-cyclohexene-1-carboxylate, diethyl 2-bromophenylphosphonate (77526-90-0), bis(4-chlorophenyl)(hydroxy)acetic acid (23851-46-9), Journal of the American Chemical Society, 75, p. 1068, 1953. Display Name: trans-cinnamic acid EC Number: 205-398-1 EC Name: trans-cinnamic acid CAS Number: 140-10-3 Molecular formula: C9H8O2 IUPAC Name: (2E)-3-phenylprop-2-enoic acid Stable. Cinnamic acid is an organic compound with the formula C6H5CH=CHCOOH. LD The alkali salts are sol in water. It is a white crystalline compound that is slightly soluble in water, and freely soluble in many organic solvents. Treatment with Cinnamic acid (CINN) of various tumor cells of epithelial and neuroectodermal origin result in dose-dependent growth inhibition following a 3-day exposure. It is a white crystalline compound that is slightly soluble in water, and freely soluble in many organic solvents. Treatment with 5 mM Cinnamic acid results in 75-95% loss of invasiveness[1]. Classified as an unsaturated carboxylic acid, it occurs naturally in a number of plants. Skip to page content; Skip to site menu on this page. cinnamic acid, (E)-Formula: C 9 H 8 O 2: Molar Mass: 148.161: Additional Names: trans-cinnamic acid (E)-cinnamic acid: 2-propenoic acid, 3-phenyl-, (E)-trans-3-phenylacrylic acid : trans-3-phenylpropenoic acid: Please be patient while the web interface loads... Property Availability . SAFETY DATA SHEET Creation Date 26-Sep-2009 Revision Date 14-Feb-2020 Revision Number 2 1. Disclaimer, Copyright © 2018 ChemSrc All Rights Reserved. Customer Support; Technical Service; … Uses advised against Food, drug, pesticide or biocidal product use. Get all suppliers and price by the below link: Reference only. Cinnamic acid CAS 140-10-3. EnvironmentalChemistry.com. Visit ChemicalBook To find more trans-Cinnamic acid(140-10-3) information like chemical properties,Structure,melting point,boiling point,density,molecular formula,molecular weight, physical properties,toxicity information,customs codes. Cinnamic acid is a monocarboxylic acid that consists of acrylic acid bearing a phenyl substituent at the 3-position. Chemsrc provides Cinnamic acid(CAS#:621-82-9) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Biologically Active Compounds | CAS Number : 621-82-9 : Molecular Formula : C9H8O2 : Molecular weight : 148.16 : EINECS : 205-398-1 : Melting point : 133 : Boiling Point : 300 : View Complete Details. PubChem Substance ID … trans-Cinnamic acid ≥99% Synonym: trans-3-Phenylacrylic acid, Cinnamic acid CAS Number 140-10-3. In addition to inhibiting tumor-cell proliferation, Cinnamic acid causes morphological changes consistent with melanocyte differentiation. Cinnamic acid and cinnamyl alcohol showed no irritation potential and no observed effect level (NOEL) for irritation caused by cinnamaldehyde was established at 1.25%. Fabrication de produits organiques Hygiène et sécurité Apparence . (E)-Cinnamic acid - chemical information, properties, structures, articles, patents and more chemical data. Solide cristallin, jaunâtre à odeur aromatique. Chemical Database Cinnamic Acid Identifications. Beilstein/REAXYS Number 1905952 . cinnamic acid per 100 ml. Identification Product Name trans-Cinnamic acid Cat No. 5 to 20 times more than for tumor cells. Liu L, et al. Properties of Cinnamic Acid: Name: Cinnamic Acid: Other Names: Cinnamylic acid, Isocinnamic acid, Benzenepropenoic acid, trans-Cinnamic acid, Phenylacrylic acid, 3-Phenylacrylic acid: Appearance: White monoclinic crystals: Molecular Formula: C 9 H 8 O 2: Melting Point: 133 °C: Boiling Point: 300 °C: Density: 1.2475 g/cm 3: Molar Mass: 148.161 g.mol –1: Solubility in Water cis-cinnamic acid: ChEBI ID CHEBI:35699: ChEBI ASCII Name cis-cinnamic acid: Definition The Z (cis) isomer of cinnamic acid: Stars This entity has been manually annotated by the ChEBI Team. Rs 850/ Kilogram Get Latest Price. About Us | Fabrication de produits organiques Hygiène et sécurité Apparence . Propriétés physiques . Mise à jour : 1986-11-10. It is also showed that 20 mM Cinnamic acid is needed to cause an IC50 in FS4 cells, i.e. The most plant phenolics are derived from trans-cinnamic acid, which is formed from l-phenylalanine by the action of l-phenylalanine ammonia-lyase (PAL), the branch point enzyme between primary (shikimate pathway) and secondary (phenyl propanoid pathway) metabolism (Fig. Solide cristallin, jaunâtre à odeur aromatique. Cells are grown for 3 days at 37°C in the presence or absence of the drug, then detached with trypsin/EDTA and counted in a Coulter counter. The change in the capacity of Cinnamic acid -treated melanoma 1011, A375(M) and SKMEL28 cells to degrade and cross tissue barriers is assessed by an in vitro invasion assay using modified Boyden chambers with matrigel-coated filters. NOEL for sensitization was determined at 2.5% and 0.5% for cinnamyl alcohol and cinnamal, respectively, while cinnamic acid is non‐sensitizing. Il est obtenu à partir de l'extrait de la cannelle, à laquelle son ester éthylique donne son odeur caractéristique, ou de certains arbustes balsamiques. Int J Cancer. Acide cinnamique Cinnamic acid for synthesis. It exists as both a cis and a trans isomer, although the latter is more common. Journals | 1995 Jul 28;62(3):345-50. It is a member of styrenes and a member of cinnamic acids. Briefly, 5 X104 cells are plated in each well of a 24-well plate, allowed to attach overnight, and treated with compounds (e.g., Cinnamic acid: 2.5, 5, 10, 20, 30 mM) the following day. Contact Seller Ask for best deal. Cinnamic acid (CA) and ferulic acid (FA) are naturally occurring phenolic acids claimed to exert beneficial effects against disorders related to oxidative stress, including cancer. Shanghai Jizhi Biochemical Technology Co., Ltd. Cinnamic acid has potential use in cancer intervention, with IC50s of 1-4.5 mM in glioblastoma, melanoma, prostate and lung carcinoma cells. MSDS/SDS Database Search | 3.3). Within 5 days of treatment with 5 mM Cinnamic acid, melanoma 1011 cells appear enlarged with a markedly increased cytoplasm-to-nuclear ratio and well organized cytoskeleton, developed long dendritic processes and became highly melanotic. Cinnamic acids play key roles in the formation of other more complex phenolic compounds. It exists as both a cis and a trans isomer, although the latter is more common. Houston, Texas 77396 US Sales: 1-800-901-7247 International Sales: 1-281-441-4400 Order Online: ScienceLab.com CHEMTREC (24HR Emergency … check more Cinnamic acid price, Home | Mise à jour : 1984-01-30. It is a self-inhibitor produced by fungal spores to prevent germination. Classified as an unsaturated carboxylic acid, it occurs naturally in a number of plants. This factor (15.8) mayvary for different spectrophotom-eters and should be determined individually for any given instrument. Growth rates are determined by cell counting. Density: 1.185g/cm 3: Melting Point: 131-136℃ Boling Point: 264.999°C at 760 mmHg: Flash Point: 189.53°C: Solubility: 0.4 g/L (20℃) Vapor Presure: 0.005mmHg at 25°C: Refractive Index: 1.616: trans-Cinnamic acid - Risk and Safety. Mise à jour : 1986-11-10. Linear Formula C 6 H 5 CH=CHCOOH . Propriétés physiques . ChemSynthesis Chemical database. Combustible. Enterprises. Articles of Cinnamic acid are included as well. Product Classification | Chemsrc provides Cinnamic acid(CAS#:621-82-9) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. A straight line relationship is obtained, which for our Beckman Model DUUltraviolet Spectro-photometer followed the equation: (density unknown-density blank) X15.8=mg. This page contains information on the chemical Cinnamic Acid including: 56 synonyms/identifiers. Cinnamic acid: a natural product with potential use in cancer intervention. A. trans-Cinnamic acid is an antimicrobial activity, with minimal inhibitory concentration (MIC) of 250 μg/mL against fish pathogen A. sobria, SY-AS1. It is a self-inhibitor produced by fungal spores to prevent germination. After 3 days of continuous treatment with Cinnamic acid, a dose-dependent loss of invasive capacity in 3 tested tumor lines is observed. The inhibitory concentrations causing a 50% reduction in tumor-cell proliferation (IC50) are between 1.2 to 4.5 mM. It has a role as a plant metabolite. Service | Cinnamic acid. LD 50 (g/kg): 3.57 orally in … Selling Leads | Create: Int J Cancer. 1995 Jul 28;62(3):345-50. , with minimal inhibitory concentration ( MIC ) of 250 μg/mL against fish pathogen A. sobria,.... Changes consistent with melanocyte differentiation, manufacturers of trans-cinnamic acid ; Utilisation et sources d'émission an carboxylic... 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Or SDS, a dose-dependent loss of invasiveness [ 1 ] system and.... Été découvert et purifié par Péligot et Dumas en 1834 activity, minimal! Sds, a dose-dependent loss of invasiveness [ 1 ] concentrations causing 50... Can also browse global suppliers, vendor, prices, Price, manufacturers of trans-cinnamic acid ; Noms:... Relationship is obtained, which for our Beckman Model DUUltraviolet Spectro-photometer followed the equation: ( unknown-density! 5 to 20 times more than for tumor cells: A13538 CAS-No 140-10-3 Synonyms 3-Phenyl-2-propenoic acid Noms... Symbols: Xi - Irritant: Risk Codes: R36/37/38 - Irritating to eyes, respiratory system and.! Organic compound with the formula C6H5CH=CHCOOH ; structure Search ; About ; GO a 50 % in... 140-10-3, synthesis, structure, density, melting point, boiling point in many organic solvents ; GO enzyme-catalyzed... In a number of plants occurs naturally in a number of plants Model DUUltraviolet Spectro-photometer followed equation. Acid bearing a phenyl substituent at the 3-position découvert et purifié par et... More than for tumor cells through enzyme-catalyzed amination to phenylalanine benzene, ether, acetone, glacial acetic,... 5 to 20 times more than for tumor cells skip to page content ; to... For sensitization was determined at 2.5 % and 0.5 % for cinnamyl alcohol and cinnamal respectively...

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