143472
3,5-Di-tert-butyl-4-hydroxybenzoic acid
98%
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この商品について
化学式:
[(CH3)3C]2C6H2(OH)CO2H
CAS番号:
分子量:
250.33
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
215-823-2
Beilstein/REAXYS Number:
2216948
MDL number:
Assay:
98%
Form:
solid
InChI key
YEXOWHQZWLCHHD-UHFFFAOYSA-N
InChI
1S/C15H22O3/c1-14(2,3)10-7-9(13(17)18)8-11(12(10)16)15(4,5)6/h7-8,16H,1-6H3,(H,17,18)
SMILES string
CC(C)(C)c1cc(cc(c1O)C(C)(C)C)C(O)=O
assay
98%
form
solid
Quality Level
mp
206-209 °C (lit.)
functional group
carboxylic acid
General description
3,5-Di-tert-butyl-4-hydroxybenzoic acid is a metabolite of butylated hydroxytoluene.
Application
3,5-Di-tert-butyl-4-hydroxybenzoic acid was used in the synthesis of antistress agents.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
保管分類
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
143472-VAR: + 143472-10G: + 143472-100G: + 143472-BULK:
jan
K Yamamoto et al.
Chemical & pharmaceutical bulletin, 39(2), 512-514 (1991-02-01)
The metabolic pathway of butylated hydroxytoluene (BHT) to the ring-oxygenated metabolites 2,6-di-tert-butylhydroquinone (BHQ) and 2,6-di-tert-butyl-p-benzoquinone (BBQ) was examined in rats. After intraperitoneal administration of 3,5-di-tert-butyl-4-hydroxybenzoic acid (BHT-acid), which had been regarded as one of the major metabolic end-products of BHT
B Spinnewyn et al.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 19(2), 139-143 (1999-02-23)
Both nitric oxide synthase (NOS) inhibitors and free radical scavengers have been shown to protect brain tissue in ischemia-reperfusion injury. Nitric oxide and superoxide anion act via distinct mechanisms and react together to form the highly deleterious peroxynitrite. Therefore the
C Park et al.
Biochemistry, 35(36), 11895-11900 (1996-09-10)
Vitreoscilla cytochrome bo ubiquinol oxidase is similar in some properties to the Escherichia coli enzyme, but unlike the latter, the Vitreoscilla oxidase functions as a primary Na+ pump. When purified Vitreoscilla cytochrome bo is incorporated into liposomes made from Vitreoscilla
H Verhagen et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 27(12), 765-772 (1989-12-01)
The kinetics and metabolism of butylated hydroxytoluene (BHT) in man and rats have been compared. Single oral doses of 200, 63 or 20 mg BHT/kg body weight were administered to rats and a single oral dose of 0.5 mg/kg body
Rosario Rodil et al.
Journal of chromatography. A, 1217(41), 6428-6435 (2010-09-08)
The development and performance evaluation of an analytical method dedicated to the comprehensive determination of the most relevant antioxidants and their metabolites in aqueous environmental samples is presented. This was achieved by a miniaturised solid-phase extraction (SPE) with 10mg Oasis
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