290823
4-tert-Octylphenol
97%
Synonym(s):
4-(1,1,3,3-Tetramethylbutyl)phenol
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All Photos(3)
About This Item
Linear Formula:
(CH3)3CCH2C(CH3)2C6H4OH
CAS Number:
Molecular Weight:
206.32
Beilstein:
513992
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
bp
175 °C/30 mmHg (lit.)
mp
79-82 °C (lit.)
solubility
water: slightly soluble 0.007 g/L at 20 °C
SMILES string
CC(C)(C)CC(C)(C)c1ccc(O)cc1
InChI
1S/C14H22O/c1-13(2,3)10-14(4,5)11-6-8-12(15)9-7-11/h6-9,15H,10H2,1-5H3
InChI key
ISAVYTVYFVQUDY-UHFFFAOYSA-N
Gene Information
mouse ... Esr1(13982)
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General description
4-tert-Octylphenol is a potential environmental pollutant and it exhibits toxic and estrogenic effects on mammalian cells. It binds to estrogen receptors and exerts estrogenic actions in vitro. The transformation of the 4-tert-octylphenol upon irradiation at 253.7nm and by hydroxyl radicals generated by the photolysis (λexc = 253.7nm) of hydrogen peroxide in aqueous solution has been studied.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
296.6 °F
Flash Point(C)
147 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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C A Blake et al.
Biology of reproduction, 57(2), 255-266 (1997-08-01)
4-Tert-octylphenol (OP) is a prevalent environmental pollutant that has been shown to exert both toxic and estrogenic effects on mammalian cells. The effects of OP on the reproductive system of adult male vertebrates are virtually unknown. In the present study
Patrick Mazellier et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2(9), 946-953 (2003-10-17)
The transformation of the organic pollutant 4-(1,1,3,3-tetramethylbutyl)phenol (4-tert-octylphenol; OP) upon irradiation at 253.7 nm and by hydroxyl radicals generated by the photolysis (lambda(exc) = 253.7 nm) of hydrogen peroxide in aqueous solution has been studied. The quantum yield of direct
C A Blake et al.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.), 216(3), 446-451 (1997-12-24)
4-tert-Octylphenol (OP) is a prevalent environmental pollutant which binds to estrogen receptors and exerts estrogenic actions in vitro. The effects of OP in vivo on mammalian female reproduction are not known. We investigated whether (i) exposure of neonatal rats to
Wen-Ling Chen et al.
Talanta, 89, 237-245 (2012-01-31)
This study developed and validated a method of measuring the feminizing chemicals 4-tert-octylphenol, 4-nonylphenol, nonylphenol monoethoxycarboxylate (NP(1)EC), nonylphenol monoethoxylate (NP(1)EO), nonylphenol diethoxylate (NP(2)EO), estrone, 17β-estradiol, estriol, 17α-ethinyl estradiol and bisphenol A in river water, sediment, and tissue using ultra-high performance
Qingxiang Zhou et al.
Talanta, 85(3), 1598-1602 (2011-08-03)
Present study described a simple, sensitive, and viable method for the determination of bisphenol A, 4-n-nonylphenol and 4-tert-octylphenol in water samples using temperature-controlled ionic liquid dispersive liquid-phase microextraction coupled to high performance liquid chromatography-fluorescence detector. In this experiment, 1-octyl-3-methylimidazolium hexafluorophosphate
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