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Merck
모든 사진(4)

주요 문서

B99901

Sigma-Aldrich

4-tert-Butylphenol

99%

동의어(들):

4-(1,1-Dimethylethyl)phenol, Butylphen, PTBP, p-tert-Butylphenol

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크기 선택

5 G
₩57,652
100 G
₩67,092
1 KG
₩160,776

₩57,652


재고 있음세부사항


벌크 견적 요청

크기 선택

보기 변경
5 G
₩57,652
100 G
₩67,092
1 KG
₩160,776

About This Item

Linear Formula:
(CH3)3CC6H4OH
CAS Number:
Molecular Weight:
150.22
Beilstein:
1817334
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
양식:
powder
분석:
99%

₩57,652


재고 있음세부사항


벌크 견적 요청

vapor pressure

1 mmHg ( 70 °C)

Quality Level

분석

99%

양식

powder

bp

236-238 °C (lit.)

mp

96-101 °C (lit.)

density

0.908 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)c1ccc(O)cc1

InChI

1S/C10H14O/c1-10(2,3)8-4-6-9(11)7-5-8/h4-7,11H,1-3H3

InChI key

QHPQWRBYOIRBIT-UHFFFAOYSA-N

유전자 정보

mouse ... Esr1(13982)
rat ... Ar(24208)

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일반 설명

4-tert-Butylphenol is a phenol derivative. Its contact with skin may lead to leukoderma. It is widely used in the polymer industry.[1] Reaction of 4-tert-Butylphenol with mushroom tyrosinase has been reported to afford 4-t-butyl-o-benzoquinone and kinetics of this enzymatic reaction has been investigated.[2]

애플리케이션

4-tert-Butylphenol is suitable reagent used in kinetic study of hydroxylation of 4-tert-butylphenol by mushroom tyrosinase.[2] It may be used in the synthesis of calix[7]arene.[3]
4-tert-Butylphenol may be employed as carbon and energy supplement in the culture medium of Sphingobium fuliginis strains.[4]

픽토그램

Health hazardCorrosionEnvironment

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Aquatic Chronic 1 - Eye Dam. 1 - Repr. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

235.4 °F - closed cup

Flash Point (°C)

113 °C - closed cup

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리 방문

이미 열람한 고객

K Thörneby-Andersson et al.
Pigment cell research, 13(1), 33-38 (2000-04-13)
Exposure of the skin to certain phenols or catechols such as 4-tert-butylphenol (TBP) and 4-tert-butylcatechol (TBC) may cause leukoderma. These substances are used in the polymer industry and numerous cases have been reported. Several theories of the mechanism for chemical
J R Ros et al.
European journal of biochemistry, 222(2), 449-452 (1994-06-01)
The reaction between 4-tert-butylphenol (BuPhOH) and mushroom tyrosinase was investigated by following 4-tert-butyl-ortho-benzoquinone, whose high stability permits the reaction to be used as a model for the study of the monophenolase activity of tyrosinase. The system evolves to a pseudo-steady
Calix [7] arene from 4-tert-butylphenol and formaldehyde.
Nakamoto Y and Ishida S-I.
Makromol. Chem., Rapid Commun., 3(10), 705-707 (1982)
J Pablo Lamas et al.
Analytical and bioanalytical chemistry, 394(8), 2231-2239 (2009-07-07)
A method for the determination of dimethyl fumarate (DMF), benzothiazole (BT) and tert-butylphenol (TBP) in desiccant and antimould agents employed for protecting consumer products from humidity and mould has been developed. The method is based on ultrasound-assisted extraction (UAE) followed
Yuka Ogata et al.
Biodegradation, 24(2), 191-202 (2012-07-11)
Although 4-tert-butylphenol (4-t-BP) is a serious aquatic pollutant, its biodegradation in aquatic environments has not been well documented. In this study, 4-t-BP was obviously and repeatedly removed from water from four different environments in the presence of Spirodela polyrrhiza, giant

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