137731
2,4-Di-tert-butylphenol
99%
동의어(들):
2,4-Bis(1,1-dimethylethyl)phenol, 2,4-Bis(tert-butyl)phenol, 2,4-Di-tert-butylhydroxybenzene, 2,4-Ditert-butylphenol
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
Linear Formula:
[(CH3)3C]2C6H3OH
CAS Number:
Molecular Weight:
206.32
Beilstein:
1910383
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
vapor pressure
1 mmHg ( 84.5 °C)
Quality Level
분석
99%
양식
solid
bp
265 °C (lit.)
mp
53-56 °C (lit.)
solubility
water: soluble 0.033 g/L at 25 °C
SMILES string
CC(C)(C)c1ccc(O)c(c1)C(C)(C)C
InChI
1S/C14H22O/c1-13(2,3)10-7-8-12(15)11(9-10)14(4,5)6/h7-9,15H,1-6H3
InChI key
ICKWICRCANNIBI-UHFFFAOYSA-N
유전자 정보
human ... GABRA1(2554)
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
2,4-Di-tert-butylphenol is isolated from the dried body of Scolopendra and possess antioxidative activity.
애플리케이션
2,4-Di-tert-butylphenol was used to study its alkylation reaction with cinnamyl alcohol in the presence of Al-substituted disordered hexagonal molecular silica catalysts.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 2
Flash Point (°F)
239.0 °F - closed cup
Flash Point (°C)
115 °C - closed cup
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
The influence of storage time and temperature on propofol concentrations in canine blood and plasma.
Sherry Cox et al.
PeerJ, 5, e3476-e3476 (2017-07-05)
Propofol is an intravenous anesthetic commonly used due to its favorable pharmacokinetic and pharmacodynamic profile. There are discrepancies in the literature about the most appropriate sample for determining propofol concentrations. Although plasma has been used for determining propofol concentrations, whole
Textural mesoporosity and the catalytic activity of mesoporous molecular sieves with wormhole framework structures.
Pauly TR, et al.
Journal of the American Chemical Society, 121(38), 8835-8842 (1999)
Jae Kwak et al.
PloS one, 11(3), e0151474-e0151474 (2016-03-12)
Male house mice produce large quantities of major urinary proteins (MUPs), which function to bind and transport volatile pheromones, though they may also function as scavengers that bind and excrete toxic compounds ('toxic waste hypothesis'). In this study, we demonstrate
Mee Kyung Sang et al.
Phytopathology, 101(6), 666-678 (2011-03-17)
We previously selected rhizobacterial strains CCR04, CCR80, GSE09, ISE13, and ISE14, which were antagonistic to Phytophthora blight of pepper. In this study, we investigated the effects of root treatment of rhizobacteria on anthracnose occurrence, ripening, and yield of pepper fruit
S Kalaichelvan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 85(1), 198-209 (2011-10-25)
In the present work, we reported a combined experimental and theoretical study on conformational stability, molecular structure and vibrational spectra of 2,4-di-tert-butylphenol (2,4-DTBP). The FT-IR (400-4000cm(-1)) and FT-Raman spectra (50-3500cm(-1)) of 2,4-DTBP were recorded. The molecular geometry, harmonic vibrational frequencies
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