모든 사진(3)
About This Item
Linear Formula:
(CH3)3CCH2C(CH3)2C6H4OH
CAS Number:
Molecular Weight:
206.32
Beilstein:
513992
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
분석
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
유전자 정보
mouse ... Esr1(13982)
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
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.
신호어
Danger
유해 및 위험 성명서
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
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
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
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
Yonglan Xu et al.
Chemosphere, 85(5), 790-796 (2011-07-13)
Direct and indirect (sensitized) photolysis of p-tert-octylphenol (OP), 4-octylphenoxy-acetic acid (OP1EC), and ibuprofen (IBU) were investigated in laboratory water and surface water under simulated and natural sunlight conditions. Photodegradation obeyed apparent-first order kinetics with rates increasing in the presence of
Tadashi Toyama et al.
Environmental science & technology, 45(15), 6524-6530 (2011-07-09)
We investigated biodegradation of technical nonylphenol (tNP) in Phragmites australis rhizosphere sediment by conducting degradation experiments using sediments spiked with tNP. Accelerated tNP removal was observed in P. australis rhizosphere sediment, whereas tNP persisted in unvegetated sediment without plants and
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