Key Documents

View All Documentation

143472

3,5-Di-tert-butyl-4-hydroxybenzoic acid

Name: 3,5-Di-<I>tert</I>-butyl-4-hydroxybenzoic acid
Brand: ALDRICH

98%

Select a Size

Change View

About This Item

Linear Formula:

[(CH₃)₃C]₂C₆H₂(OH)CO₂H

CAS Number:

1421-49-4

Molecular Weight:

250.33

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24848587

EC Number:

215-823-2

Beilstein/REAXYS Number:

2216948

MDL number:

MFCD00008827

Assay:

98%

Form:

solid

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Quality Level

100

assay

98%

form

solid

mp

206-209 °C (lit.)

functional group

carboxylic acid

SMILES string

CC(C)(C)c1cc(cc(c1O)C(C)(C)C)C(O)=O

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)

InChI key

YEXOWHQZWLCHHD-UHFFFAOYSA-N

Description

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.

pictograms

GHS07

signalword

Warning

hcodes

H302,H315,H319,H335

pcodes

P261 - P264 - P270 - P301 + P312 - P302 + P352 - P305 + P351 + P338

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:

Certificates of Analysis (COA)

Lot/Batch Number

11422DJ

03312DY

11201KW

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Disposition of single oral doses of butylated hydroxytoluene in man and rat.

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

Determination of synthetic phenolic antioxidants and their metabolites in water samples by downscaled solid-phase extraction, silylation and gas chromatography-mass spectrometry.

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

Further metabolism of 3,5-di-tert-butyl-4-hydroxybenzoic acid, a major metabolite of butylated hydroxytoluene, in rats.

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

View All Related Papers

Global Trade Item Number

SKU	GTIN
143472-10G	04061838734860