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3-Indolebutyric acid | CAS:133-32-4

3-Indolebutyric acid

名称：3-吲哚丁酸 | 3-Indolebutyric acid
CAS号：133-32-4
别名：4-(3-1H-Indolyl)butyric acid; 4-(3-Indolyl)butyric acid ; Indole-3-butyric acid; Hormodin; Seradix
分子式：C₁₂H₁₃NO₂
分子量：203.24
EINESC号：205-101-5

产品描述

物理化学性质

熔点	120-125 ºC

安全数据

危险品标志	T
危险类别码	R25;R36/37/38
安全说明书	S26;S28A;S36/37/39;S38;S45

SDS

来源	SDS样本
没有数据	没有数据

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Dietary supplementation with cocoa flavanols does not alter colon tissue profiles of native flavanols and their microbial metabolites established during habitual dietary exposure in C57BL/6J mice.Katheryn M Goodrich et al.Journal of agricultural and food chemistry, 62(46), 11190-11199 (2014-10-23) Intracellular degradation of two structurally different polyhydroxyalkanoic acids accumulated in Pseudomonas putida and Pseudomonas citronellolis from mixtures of octanoic acid and 5-phenylvaleric acid.D M Chung et al.International journal of biological macromolecules, 29(4-5), 243-250 (2001-11-24) Species Differences in the Binding of Sodium 4-Phenylbutyrate to Serum Albumin.Keishi Yamasaki et al.Journal of pharmaceutical sciences, 106(9), 2860-2867 (2017-05-01) Metabolism of dietary procyanidins in rats.Marie-Paule Gonthier et al.Free radical biology & medicine, 35(8), 837-844 (2003-10-15) Specificity of procaine and ester hydrolysis by human, minipig, and rat skin and liver.Christopher Jewell et al.Drug metabolism and disposition: the biological fate of chemicals, 35(11), 2015-2022 (2007-08-01) Structure and polymer form of poly-3-hydroxyalkanoates produced by Pseudomonas oleovorans grown with mixture of sodium octanoate/undecylenic acid and sodium octanoate/5-phenylvaleric acid.I-Ching Ho et al.International journal of biological macromolecules, 40(2), 112-118 (2006-08-22) Phenylvaleric acid and flavonoid glycosides from Polygonum salicifolium.I Calis et al.Journal of natural products, 62(8), 1101-1105 (1999-09-10)

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名称	CAS号

产品描述

物理化学性质

安全数据

SDS

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