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Merck
CN

112046

2-甲基-2-丙烯-1-醇

98%

别名:

β-甲基烯丙醇, “异丁烯醇"

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关于此项目

线性分子式:
CH2=C(CH3)CH2OH
化学文摘社编号:
分子量:
72.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-161-0
Beilstein/REAXYS Number:
969226
MDL number:
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产品名称

2-甲基-2-丙烯-1-醇, 98%

InChI key

BYDRTKVGBRTTIT-UHFFFAOYSA-N

InChI

1S/C4H8O/c1-4(2)3-5/h5H,1,3H2,2H3

SMILES string

CC(=C)CO

assay

98%

refractive index

n20/D 1.426 (lit.)

bp

113-115 °C (lit.)

density

0.857 g/mL at 25 °C (lit.)

functional group

hydroxyl

Quality Level

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Application

2-甲基-2-丙烯-1-醇 (MePro) 附着在半纤维素乙酰化半乳葡萄糖甘露聚糖 (AcGGM) 主链上,为其提供侧链位点,允许随后的交联和水凝胶形成

General description

2-甲基-2-丙烯-1-醇 (MePro) 与 OH 自由基气相反应的速率系数可采用相对速率法或脉冲激光光解-激光诱导荧光技术

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

89.6 °F - closed cup

flash_point_c

32 °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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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Alkenyl-Functionalized Precursors for Renewable Hydrogels Design.
Journal of Polymer Science Part A: Polymer Chemistry, 47(17), 3595-3606 (2009)
Pablo M Cometto et al.
The journal of physical chemistry. A, 112(19), 4444-4450 (2008-04-25)
Rate coefficients for the gas-phase reactions of OH radicals with four unsaturated alcohols, 3-methyl-3-buten-1-ol (k1), 2-buten-1-ol (k2), 2-methyl-2-propen-1-ol (k3) and 3-buten-1-ol (k4), were measured using two different techniques, a conventional relative rate method and the pulsed laser photolysis-laser induced fluorescence
R Bittman et al.
Chemistry and physics of lipids, 50(2), 99-103 (1989-05-01)
The synthesis of C2-methyl-1,2-di-O-hexadecylglycerophosphocholine from methylallyl alcohol is described and the 13C-NMR assignments of all glycerol backbone and headgroup resonances are provided. Bond rotations in the glycerol backbone of this diether phospholipid derivative are impeded by steric hindrance exerted by

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