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B97208

Sigma-Aldrich

2-tert-Butyl-4-methylphenol

99%

Synonym(s):

2-tert-Butyl-p-cresol

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About This Item

Linear Formula:
(CH3)3CC6H3(CH3)OH
CAS Number:
2409-55-4
Molecular Weight:
164.24
Beilstein:
1817645
EC Number:
219-314-6
MDL number:
MFCD00002381
UNSPSC Code:
12352100
PubChem Substance ID:
24892152
NACRES:
NA.22

Assay

99%

form

crystals

bp

244 °C (lit.)

mp

50-52 °C (lit.)

SMILES string

Cc1ccc(O)c(c1)C(C)(C)C

InChI

1S/C11H16O/c1-8-5-6-10(12)9(7-8)11(2,3)4/h5-7,12H,1-4H3

InChI key

IKEHOXWJQXIQAG-UHFFFAOYSA-N

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Pictograms

CorrosionEnvironment
GHS05,GHS09

Signal Word

Danger

Hazard Statements

H314,H411

Hazard Classifications

Aquatic Chronic 2 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 2

Flash Point(F)

212.0 °F - closed cup

Flash Point(C)

100 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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P Lambelet et al.
Skin pharmacology : the official journal of the Skin Pharmacology Society, 1(2), 115-121 (1988-01-01)
Radical reactions of anthralin and its metabolites with skin have been studied by ESR spectroscopy. The influence of compounds which are known to suppress inflammation are described. The ESR spectra recorded during the reaction of anthralin with skin were essentially
M Hirose et al.
Cancer research, 51(3), 824-827 (1991-02-01)
The combined effects of low doses of promoters or carcinogens on two-stage forestomach carcinogenesis were examined in rats pretreated with N-methyl-N'-nitro-N-nitrosoguanidine. Groups of 15 rats were given a single 150 mg/kg body weight intragastric dose of N-methyl-N'-nitro-N-nitrosoguanidine. Starting 1 week
Y Kurata et al.
Japanese journal of cancer research : Gann, 81(8), 754-759 (1990-08-01)
The urinary bladder tumor-promoting potentials of the phenolic antioxidants, 2-tert-butyl-4-methylphenol (TBMP), propylparaben, catechol, resorcinol and hydroquinone, which are structurally related to butylated hydroxyanisole (BHA), were investigated in 170 male F344 rats. The animals were initially given 0.05% N-butyl-N-(4-hydroxybutyl)nitrosamine (BBN) as
Shudong Zhang et al.
AAPS PharmSciTech, 20(2), 75-75 (2019-01-12)
Drugs with pH-dependent solubility that have poor water solubility can be identified in the drug discovery pipeline. Some of them have poor oral absorption, which can result in insufficient efficacy. Micro-environmental pH-modifying solid dispersion (micro pHm SD) is a promising
M A Shibata et al.
Carcinogenesis, 11(3), 425-429 (1990-03-01)
The effects of 8 weeks of oral administration of five different phenolic antioxidants, e.g. catechol (CC), resorcinol, hydroquinone (HQ), 2-tert-butyl-4-methylphenol (TBMP) and propylparabene (PP), on forestomach and glandular stomach epithelium of male F344 rats were evaluated using a combined immunohistochemical
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