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20021

3-叔丁基-4-羟基苯甲醚

Name: 3-<I>叔丁基</I>-4-羟基苯甲醚
Brand: ALDRICH

≥98% (sum of isomers, GC), ≤10% 2-BHA basis (GC)

别名:

2-叔丁基-4-甲氧基苯酚, 3-BHA, BHA

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关于此项目

经验公式（希尔记法）:

C₁₁H₁₆O₂

化学文摘社编号:

121-00-6

分子量:

180.24

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

57647769

EC Number:

204-442-7

Beilstein/REAXYS Number:

1867499

MDL number:

MFCD00040484

Assay:

≥98% (sum of isomers, GC)

Form:

solid

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属性

Quality Level

200

assay

≥98% (sum of isomers, GC)

form

solid

composition

2-BHA, ≤10% GC , 3-BHA, ≥90% GC

impurities

≤1% 4-hydroxyanisole

ign. residue

≤0.05%

mp

48-63 °C

solubility

ethanol: soluble 1 g/10 mL, clear, colorless to faint yellow or tan

SMILES string

COc1ccc(O)c(c1)C(C)(C)C

InChI

1S/C11H16O2/c1-11(2,3)9-7-8(13-4)5-6-10(9)12/h5-7,12H,1-4H3

InChI key

MRBKEAMVRSLQPH-UHFFFAOYSA-N

说明

General description

研究了 3--叔 -丁基-4-羟基苯甲醚在酞菁镍（作为电子媒介体）修饰的聚合物电极上的伏安行为。

Application

调节间充质干细胞中的Smad信号通路：3-叔丁基-4-羟基苯甲醚通过调节Smad信号通路干扰C3H10T1/2间充质干细胞向褐色脂肪细胞的分化，揭示它在肥胖症和代谢综合征研究中的潜在应用(Wang et al., 2023)。

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Hazard Classifications

Aquatic Chronic 2

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Voltammetric determination of the phenolic antioxidants 3-tert-butyl-4-hydroxyanisole and tert-butylhydroquinone at a polypyrrole electrode modified with a nickel phthalocyanine complex.

C de la Fuente et al.

Talanta, 49(2), 441-452 (2008-10-31)

The voltammetric behaviour of the antioxidants 3-tert-butyl-4-hydroxyanisole (BHA) and tert-butylhydroquinone (TBHQ), at a polymer electrode modified with nickel phthalocyanine as electron mediator, is described, and an electroanalytical method for the determination of these antioxidants based on their electrochemical oxidation on

Identification and structure characterization of S-containing metabolites of 3-tert-butyl-4-hydroxyanisole in rat urine and liver microsomes.

K Tajima et al.

Drug metabolism and disposition: the biological fate of chemicals, 19(6), 1028-1033 (1991-11-01)

After ip administration of 3-tert-butyl-4-hydroxyanisole (3-BHA) to rats, two previously undocumented metabolites 2-tert-butyl-5-methylthiohydroquinone (TBHQ-5-SMe) and 2-tert-butyl-6-methylthiohydroquinone (TBHQ-6-SMe) were identified in the urine by comparison with the authentic samples by GC/MS. In addition to these metabolites, 3-tert-butyl-4,5-dihydroxyanisole was also detected in

Induction of oxidative DNA damage and early lesions in rat gastro-intestinal epithelium in relation to prostaglandin H synthase-mediated metabolism of butylated hydroxyanisole.

P A Schilderman et al.

Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 33(2), 99-109 (1995-02-01)

The effect of metabolic activation of the food additive 3-tert-butyl-4-hydroxyanisole (BHA) by prostaglandin H synthase on the gastro-intestinal cell proliferation was determined by studies of the nature and the time dependency of early lesions in the forestomach, glandular stomach and

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20021-100G	04061835176823