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Merck
CN

V001467

甲醇

p.a., 99.9%

别名:

木酒精

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线性分子式:
CH3OH
化学文摘社编号:
分子量:
32.04
EC Number:
200-659-6
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1098229
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vapor density

1.11 (vs air)

vapor pressure

410 mmHg ( 50 °C), 97.68 mmHg ( 20 °C)

grade

p.a.

assay

99.9%

autoignition temp.

725 °F

mp

−98 °C (lit.)

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General description

Methanol (carbinol or methyl alcohol or wood alcohol) is a primary aliphatic alcohol miscible in water. It′s a polar solvent used in many organic synthesis reactions. Recently, it has been used in direct methanol fuel cell (DMFC) technology and in the production of gasoline, olefins, and hydrocarbons.

Application

Methanol can be used:
  • In combination with magnesium as a reagent for the reduction of ozonides and peroxides chemoselectively.
  • In combination with NaNO2 and HCl as a reagent in the diazotization of arylamines.
  • As a solvent in many organic reactions like C-C bond cleavage, reduction, cycloaddition, and amination.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

target_organs

Eyes,Central nervous system

存储类别

3 - Flammable liquids

wgk

WGK 2

flash_point_f

49.5 °F - closed cup

flash_point_c

9.7 °C - closed cup

法规信息

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分析证书(COA)

Lot/Batch Number

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Magnesium/methanol: An effective reducing agent for peroxides
Dai P, et al.
The Journal of Organic Chemistry, 69(8), 2851-2852 (2004)
One-pot sequential 1, 4-and 1, 2-reductions of α,β-unsaturated δ-lactones to the corresponding δ-lactols with CuCl and NaBH4 in methanol
Matsumoto Y and Yonaga M
Synlett, 25(12), 1764-1768 (2014)
A new simplified protocol for copper (I) alkyne-azide cycloaddition reactions using low substoichiometric amounts of copper (II) precatalysts in methanol
Buckley B, et al.
Synlett, 27(01), 51-56 (2016)
A reductive amination of carbonyls with amines using decaborane in methanol
Bae J, et al.
Journal of the Chemical Society, Part 1, 27(2), 145-146 (2000)
Methanol-promoted Borylation of Arylamines: A simple and green synthetic method to Arylboronic acids and Arylboronates
Zhao C, et al.
Synlett, 25(11), 1577-1584 (2014)

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