143472
3,5-Di-tert-butyl-4-hydroxybenzoic acid
98%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
[(CH3)3C]2C6H2(OH)CO2H
CAS Number:
Molecular Weight:
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
mp
206-209 °C (lit.)
functional group
carboxylic acid
Quality Level
Looking for similar products? Visit Product Comparison Guide
Related Categories
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
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
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
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
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
Wei Wang et al.
Environment international, 128, 24-29 (2019-04-29)
Synthetic phenolic antioxidants (SPAs) such as 2,6-di-tert-butyl-4-hydroxytoluene (butylated hydroxytoluene, BHT), are used in a wide variety of consumer products, including certain foodstuffs (e.g. fats and oils) and cosmetics. Although BHT is considered generally safe as a food preservative when used
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service