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Merck
CN

111120

2-甲基-2-戊醇

99%

别名:

二甲基丙基甲醇

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线性分子式:
CH3CH2CH2C(CH3)2OH
化学文摘社编号:
分子量:
102.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-681-0
Beilstein/REAXYS Number:
1718951
MDL number:
Assay:
99%
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产品名称

2-甲基-2-戊醇, 99%

InChI key

WFRBDWRZVBPBDO-UHFFFAOYSA-N

InChI

1S/C6H14O/c1-4-5-6(2,3)7/h7H,4-5H2,1-3H3

SMILES string

CCCC(C)(C)O

assay

99%

refractive index

n20/D 1.411 (lit.)

bp

120-122 °C (lit.)

mp

−109-−107 °C (lit.)

density

0.835 g/mL at 25 °C (lit.)

functional group

hydroxyl

Quality Level

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Application

2-甲基-2-戊醇已被用于研究其拮抗剂活性。它可与第二个靶标位点反应以改变其疏水性激动剂结合位点和变构位点之间的空间关系

General description

2-甲基-2-戊醇是一种在暴露于甲基戊烷的大鼠尿液中发现的代谢物

pictograms

FlameExclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

86.0 °F - closed cup

flash_point_c

30 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品
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分析证书(COA)

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Michael F Wilkemeyer et al.
Molecular pharmacology, 62(5), 1053-1060 (2002-10-23)
1-Octanol antagonizes ethanol inhibition of L1-mediated cell adhesion and prevents ethanol teratogenesis in mouse whole embryo culture. Herein, we identify a new series of alcohol antagonists and study their mechanism of action. Cell aggregation assays were carried out in ethanol-sensitive
T Kawai et al.
Occupational and environmental medicine, 52(11), 757-763 (1995-11-01)
To investigate the possibilities of personal ambient monitoring and biological monitoring for methylpentane isomers. The performance of activated carbon cloth to absorb 2- and 3-methylpentane was studied by experimental vapour exposure followed by solvent extraction and gas chromatography (GC). Urine
Alfonso Pérez-Garrido et al.
Bioorganic & medicinal chemistry, 17(2), 896-904 (2008-12-06)
This paper reports a QSAR study for predicting the complexation of a large and heterogeneous variety of substances (233 organic compounds) with beta-cyclodextrins (beta-CDs). Several different theoretical molecular descriptors, calculated solely from the molecular structure of the compounds under investigation

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