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Key Documents

W284300

Sigma-Aldrich

4-Pentenoic acid

≥98%, stabilized, FG

동의어(들):

3-Vinylpropionic acid, Allylacetic acid

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About This Item

Linear Formula:
CH2=CHCH2CH2COOH
CAS Number:
Molecular Weight:
100.12
FEMA Number:
2843
Beilstein:
1633696
EC Number:
유럽평의회 번호:
2004
MDL number:
UNSPSC 코드:
12164502
PubChem Substance ID:
플래비스(Flavis) 번호:
8.048
NACRES:
NA.21

생물학적 소스

synthetic

Quality Level

Grade

FG
Halal
Kosher

Agency

meets purity specifications of JECFA

규정 준수

EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 172.515

vapor density

>1 (vs air)

분석

≥98%

포함

α-tocopherol, synthetic as stabilizer

refractive index

n20/D 1.428 (lit.)

bp

83-84 °C/12 mmHg (lit.)

mp

−22.5 °C (lit.)

density

0.981 g/mL at 25 °C (lit.)

응용 분야

flavors and fragrances

문건

see Safety & Documentation for available documents

식품 알레르기항원

no known allergens

감각 수용성의

cheese

SMILES string

OC(=O)CCC=C

InChI

1S/C5H8O2/c1-2-3-4-5(6)7/h2H,1,3-4H2,(H,6,7)

InChI key

HVAMZGADVCBITI-UHFFFAOYSA-N

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일반 설명

4-Pentenoic acid is a volatile acid reported to be found in tobacco.

픽토그램

CorrosionExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point (°F)

192.2 °F - closed cup

Flash Point (°C)

89 °C - closed cup

개인 보호 장비

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

Steam volatile acids of Latakia tobacco leaf.
Creasy PJ & Saxby MJ.
Phytochemistry, 8(12), 2427-2429 (1969)
Effects of flue-curing and ageing on the volatile, neutral and acidic constituents of Virginia tobacco.
Wahlberg I, et al.
Phytochemistry, 16(8), 1217-1231 (1977)
J F Pouliot et al.
Canadian journal of physiology and pharmacology, 70(9), 1247-1253 (1992-09-01)
Fanconi's syndrome was investigated using brush border membrane (BBM) vesicles isolated from dog kidney. Sodium-dependent uptake of glucose, phosphate, and amino acids and protein phosphorylation were studied in BBM isolated from normal and from 4-pentenoate- and maleate-treated animals. The time
Y Boulanger et al.
Magnetic resonance in medicine, 28(1), 137-144 (1992-11-01)
The metabolism of 4-pentenoate in isolated kidney tubules has been investigated by 1H and 13C NMR. The 4-pentenoate metabolite, 3-keto-4-pentenoyl-CoA, accumulated in proximal tubules only and its formation could be competitively inhibited by octanoate. 4-Pentenoate was metabolized in thick ascending
K Kassahun et al.
Drug metabolism and disposition: the biological fate of chemicals, 21(6), 1098-1106 (1993-11-01)
The terminal olefin metabolite of valproic acid (VPA), 4-ene VPA, is an analog of the experimental hepatotoxin 4-pentenoic acid and is believed to play a role in the hepatotoxicity of VPA. The formation of glutathione and N-acetylcysteine conjugates of the

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