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Merck
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Principaux documents

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155322

Sigma-Aldrich

trans-Styrylacetic acid

greener alternative

96%

Synonyme(s) :

4-Phenyl-3-butenoic acid

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About This Item

Formule linéaire :
C6H5CH=CHCH2CO2H
Numéro CAS:
1914-58-5
Poids moléculaire :
162.19
Numéro MDL:
MFCD00002783
Code UNSPSC :
12352100
ID de substance PubChem :
24849516
Nomenclature NACRES :
NA.22
Essai:
96%

Niveau de qualité

100

Essai

96%

Score du produit alternatif plus écologique

old score: 22
new score: 3
Find out more about DOZN™ Scoring

Caractéristiques du produit alternatif plus écologique

Atom Economy
Design for Energy Efficiency
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

Pf

84-86 °C (lit.)

Groupe fonctionnel

carboxylic acid
phenyl

Autre catégorie plus écologique

, Re-engineered

Chaîne SMILES 

OC(=O)C\C=C\c1ccccc1

InChI

1S/C10H10O2/c11-10(12)8-4-7-9-5-2-1-3-6-9/h1-7H,8H2,(H,11,12)/b7-4+

Clé InChI

PSCXFXNEYIHJST-QPJJXVBHSA-N

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Catégories apparentées

Description générale

The polarized IR spectra of the hydrogen bond system in trans-styrylacetic acid has been studied.
We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product belongs to category of Re-engineered products, showing key improvements in Green Chemistry Principles “Atom Economy”, “Design for Energy Efficiency” and “Use of Renewable Feedstock”. Click here to view its DOZN scorecard.

Application

trans-Styrylacetic acid (4-Phenyl-3-butenoic acid) was used as mechanism-based inhibitor of Peptidylglycine α-hydroxylating monooxygenase.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H315,H319,H335

Classification des risques

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number
MKCL5502
MKCK3988
MKCH9877
MKCH3033
MKCH4550

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Henryk T Flakus et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 65(2), 481-489 (2006-03-11)
We have investigated the polarized IR spectra of the hydrogen bond system in crystals of trans-styrylacetic acid C(6)H(5)CHCHCH(2)COOH, and also in crystals of the following three deuterium isotopomers of the compound: C(6)H(5)CHCHCH(2)COOD, C(6)H(5)CHCHCD(2)COOH and C(6)H(5)CHCHCD(2)COOD. The spectra were measured at
J Scognamiglio et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 50 Suppl 2, S120-S123 (2011-10-29)
A toxicologic and dermatologic review of 4-phenyl-3-buten-2-ol when used as a fragrance ingredient is presented. 4-Phenyl-3-buten-2-ol is a member of the fragrance structural group Aryl Alkyl Alcohols and is a secondary alcohol. The AAAs are a structurally diverse class of
Yuan-Ning Cao et al.
Regulatory peptides, 113(1-3), 109-114 (2003-04-11)
Human adrenomedullin (hAM) is an endogenous peptide that has potent vasodilator activity. Mature AM is biosynthesized from its intermediate form, glycine-extended AM (AM-gly), by carboxy-terminal amidation. AM-gly is generally considered to be biologically inactive but is a major molecular form
David J Merkler et al.
Biochemistry, 43(39), 12667-12674 (2004-09-29)
Oleamide is an endogenous sleep-inducing lipid that has been isolated from the cerebrospinal fluid of sleep-deprived mammals. Oleamide is the best-understood member of the primary fatty acid amide family. One key unanswered question regarding oleamide and all other primary acid
W J Driscoll et al.
Biochemistry, 39(27), 8007-8016 (2000-07-13)
The bifunctional enzyme peptidylglycine-alpha-amidating monooxygenase mediates the conversion of C-terminal glycine-extended peptides to their active alpha-amidated products. Peptidylglycine-alpha-hydroxylating monooxygenase (PHM, EC 1.14.17. 3) catalyzes the first reaction in this two-step process. The olefinic compound 4-phenyl-3-butenoic acid (PBA) is the most
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