152463
2-Methyl-2-butanol
ReagentPlus®, 99%
동의어(들):
tert-Amyl alcohol, tert-Pentyl alcohol
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH3CH2C(CH3)2OH
CAS 번호:
Molecular Weight:
88.15
Beilstein:
1361351
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.21
Bp:
102 °C (lit.)
Vapor pressure:
12 mmHg ( 20 °C)
vapor density
3 (vs air)
Quality Level
vapor pressure
12 mmHg ( 20 °C)
제품 라인
ReagentPlus®
분석
99%
양식
liquid
autoignition temp.
819 °F
expl. lim.
9 %
dilution
(for general lab use)
refractive index
n20/D 1.405 (lit.)
pH
6.0 (20 °C, 118 g/L)
bp
102 °C (lit.)
mp
−12 °C (lit.)
density
0.805 g/mL at 25 °C (lit.)
SMILES string
CCC(C)(C)O
InChI
1S/C5H12O/c1-4-5(2,3)6/h6H,4H2,1-3H3
InChI key
MSXVEPNJUHWQHW-UHFFFAOYSA-N
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일반 설명
2-Methyl-2-butanol is an isomeric form of pentanol. Various physical properties (static dielectric constant, viscosity, density, ultrasonic and dielectric relaxation) of 2-methyl-2-butanol have been evaluated over a wide range of temperatures. Its ability as solvent in the extraction of furfural from aqueous solutions has been tested. Kinetic parameters of the three-phase reaction of MBY with hydrogen catalyzed by a commercial palladium-based catalyst in the absence of solvent have been described.
애플리케이션
2-Methyl-2-butanol (tert-amyl alcohol, t-AmylOH, MBY) has been used as solvent for the dissolution of avertin [2,2,2-tribromoethanol), which was employed as an anesthetic in immunohistochemical study. It has been used in the preparation of (E)-2-(2-(3-ethoxy-3-oxoprop-1-enyl)-6-fluorophenyl)acetic acid.
법적 정보
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Central nervous system, Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point (°F)
68.9 °F - closed cup
Flash Point (°C)
20.5 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
General kinetic modeling of the selective hydrogenation of 2-methyl-3-butyn-2-ol over a commercial palladium-based catalyst.
Vernuccio S, et al.
Industrial & Engineering Chemistry Research, 54(46), 11543-11551 (2015)
Astrid L Basse et al.
Molecular metabolism, 53, 101271-101271 (2021-06-14)
NAD+ is a co-factor and substrate for enzymes maintaining energy homeostasis. Nicotinamide phosphoribosyltransferase (NAMPT) controls NAD+ synthesis, and in skeletal muscle, NAD+ is essential for muscle integrity. However, the underlying molecular mechanisms by which NAD+ synthesis affects muscle health remain
Molecular association and dynamics in n-pentanol and 2-methyl-2-butanol: Ultrasonic, dielectric and viscosity studies at various temperatures.
D'Aprano A, et al.
Molecular Physics, 55(2), 475-488 (1985)
Ligand--Accelerated ortho--C-H Olefination of Phenylacetic Acids.
Engle KM, et al.
Organic Syntheses, 92, 58-75 (2015)
Liwen Zhang et al.
STAR protocols, 2(4), 100792-100792 (2021-10-12)
This protocol describes the generation of a mouse colorectal cancer (CRC) model to study the mechanism of CRC growth and metastasis. Compared to existing protocols, this protocol is mainly to improve the incidence of metastasis. The major advantage of this
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