112046
2-Methyl-2-propen-1-ol
98%
Synonym(s):
β-Methallyl alcohol
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About This Item
Linear Formula:
CH2=C(CH3)CH2OH
CAS Number:
Molecular Weight:
72.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-161-0
Beilstein/REAXYS Number:
969226
MDL number:
Assay:
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%
Quality Level
bp
113-115 °C (lit.)
density
0.857 g/mL at 25 °C (lit.)
functional group
hydroxyl
Related Categories
General description
The rate coefficient for gas-phase reaction of 2-Methyl-2-propen-1-ol (MePro) with OH radical can be determined by the relative rate method or by using the pulsed laser photolysis-laser induced fluorescence technique.
Application
2-Methyl-2-propen-1-ol (MePro) attaches to hemicellulose acetylated galactoglucomannan (AcGGM) backbone providing it with pendant sites that allow subsequent cross-linking and hydrogel formation.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
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
Regulatory Information
危险化学品
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Alkenyl-Functionalized Precursors for Renewable Hydrogels Design.
Journal of Polymer Science Part A: Polymer Chemistry, 47(17), 3595-3606 (2009)
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
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
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