B97208
2-tert-Butyl-4-methylphenol
99%
Synonym(s):
2-tert-Butyl-p-cresol
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100 G
$68.00
500 G
$224.77
About This Item
Linear Formula:
(CH3)3CC6H3(CH3)OH
CAS Number:
Molecular Weight:
164.24
Beilstein/REAXYS Number:
1817645
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
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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signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk_germany
WGK 2
flash_point_f
212.0 °F - closed cup
flash_point_c
100 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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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
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
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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