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Merck
CN
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安全信息

137561

Sigma-Aldrich

3-甲基-1-戊炔-3-醇

98%

别名:

催眠醇, 甲基乙基乙炔基甲醇

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About This Item

线性分子式:
CH≡CC(OH)(CH3)CH2CH3
CAS号:
77-75-8
分子量:
98.14
Beilstein:
969340
EC 号:
201-055-5
MDL编号:
MFCD00004479
UNSPSC代码:
12352100
PubChem化学物质编号:
24848336
NACRES:
NA.22

蒸汽密度

3 (vs air)

质量水平

100

蒸汽压

6.5 mmHg ( 20 °C)

方案

98%

表单

liquid

折射率

n20/D 1.431 (lit.)

沸点

121-122 °C (lit.)

溶解性

Cellosolve: miscible
Stoddard solvent: miscible
acetone: miscible
benzene: miscible
carbon tetrachloride: miscible
cyclohexanone: miscible
diethyl ether: soluble
diethylene glycol: miscible
ethanolamine: miscible
ethyl acetate: miscible
kerosene: miscible
mineral spirits: miscible
neatsfoot oil: miscible
petroleum ether: miscible
soybean oil: miscible

密度

0.866 g/mL at 25 °C (lit.)

官能团

hydroxyl

SMILES字符串

CCC(C)(O)C#C

InChI

1S/C6H10O/c1-4-6(3,7)5-2/h1,7H,5H2,2-3H3

InChI key

QXLPXWSKPNOQLE-UHFFFAOYSA-N

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相关类别

一般描述

3-Methyl-1-pentyn-3-ol acts as initiator during the synthesis of propargyl-terminated polylactide by bulk ring-opening polymerization.

应用

3-Methyl-1-pentyn-3-ol is propargyl alcohol that can be used as:
  • A reactant to synthesize α-methylene cyclic carbonates by reacting with carbon dioxide.
  • A reactant in the synthesis of 2,6,9-trisubstituted purine based CDK inhibitors.
  • An initiator in the synthesis of polylactide bearing terminal propargyl group via ring-opening polymerization of L-lactide.

生化/生理作用

3-Methyl-1-pentyn-3-ol is a sedative and induces hepatic P4503A in mouse.

警示用语：

Danger

危险分类

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 3

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

82.4 °F - closed cup

闪点(°C)

28 °C - closed cup

个人防护装备

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

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCX1253
MKCV9890
MKCP1836
MKCH7830
MKCD3994

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Cyclin-dependent kinase (CDK) inhibitors: development of a general strategy for the construction of 2, 6, 9-trisubstituted purine libraries. Part 3
Brun V, et al.
Tetrahedron Letters, 42(46), 8169-8171 (2001)
Preparation of propargyl-terminated polylactide by the bulk ring-opening polymerization.
Liu X, et al.
Journal of Macromolecular Science, Part A: Pure and Applied Chemistry, 46(10), 937-942 (2009)
H Teräväinen et al.
Journal of neurology, neurosurgery, and psychiatry, 49(2), 198-199 (1986-02-01)
Six patients with essential tremor tested in the therapeutic effectiveness of a 6-carbon alcohol, methylpentynol, 200 mg/day, against placebo in a randomised double-blind clinical cross-over trial. The effect of methylpentynol on postural tremor amplitude was not different from that of
M I Walash et al.
Journal - Association of Official Analytical Chemists, 68(6), 1209-1212 (1985-11-01)
Titrimetric and spectrophotometric titration methods are described for the quantitative determination of acetylenic hypnotics ethchlorvynol, ethinamate, and meparfynol carbamate as pure substances and in dosage forms. The methods involve the use of different brominating agents. A known excess of the
Yanlong Gu et al.
The Journal of organic chemistry, 69(2), 391-394 (2004-01-17)
Reactions of propargylic alcohols with CO(2) in a [BMIm][PhSO(3)]/CuCl catalytic system to produce the corresponding alpha-methylene cyclic carbonates were conducted with high yields. Mild reaction conditions, enhanced rates, improved yields, and recyclable ionic liquid catalyst systems are the remarkable features
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