375721
2-Methyl-1,3-propanediol
99%
동의어(들):
1,3-Dihydroxy-2-methylpropane, 2-Methylpropan-1,3-diol, Methylpropanediol
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모든 사진(1)
About This Item
Linear Formula:
CH3CH(CH2OH)2
CAS Number:
Molecular Weight:
90.12
Beilstein:
1731422
EC Number:
MDL number:
UNSPSC 코드:
12162002
PubChem Substance ID:
NACRES:
NA.23
추천 제품
vapor density
3.2 (vs air)
분석
99%
양식
liquid
refractive index
n20/D 1.445 (lit.)
bp
123-125 °C/20 mmHg (lit.)
mp
−91 °C (lit.)
density
1.015 g/mL at 25 °C (lit.)
SMILES string
CC(CO)CO
InChI
1S/C4H10O2/c1-4(2-5)3-6/h4-6H,2-3H2,1H3
InChI key
QWGRWMMWNDWRQN-UHFFFAOYSA-N
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일반 설명
2-Methyl-1,3-propanediol is a biodegradable, colorless glycol. This low molecular weight compound has no significant hazard potential and is widely used in polymer and coating applications.
애플리케이션
2-Methyl-1,3-propanediol is used:
- In the preparation of solid polymer electrolytes for lithium metal batteries.
- To obtain methyl methacrylate (precursor for polymethyl methacrylate glass) via a partial oxidation process.
- In the synthesis of biodegradable thermoplastic elastomer by condensation reaction.
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point (°F)
260.6 °F - closed cup
Flash Point (°C)
127 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
이미 열람한 고객
J Fowles et al.
Regulatory toxicology and pharmacology : RTP, 91, 240-248 (2017-11-04)
2-methyl 1,3-propandiol (MPD) is a low molecular weight, colorless glycol used in polymer and coating applications. The log Kow of -0.6 suggests partitioning to aqueous phases with a low concern for possible bioaccumulation. MPD was found to be inherently biodegradable.
Zhi-Yu Yang et al.
Soft matter, 16(2), 402-410 (2019-12-04)
A series of bio-based poly(propylene-co-2-methyl-1,3-propanediol 2,5-furandicarboxylate) (PPMF) copolyesters, with various compositions from poly(propylene 2,5-furandicarboxylate) (PPF) to poly(2-methyl-1,3-propylene 2,5-furandicarboxylate) (PMePF), were synthesized by conventional melt polymerization. The effects of the substituent group to PPF on the thermal properties, mechanical properties, and
Juri Maeda et al.
Biochimica et biophysica acta, 1861(8), 2112-2118 (2017-04-30)
Due to the strict enantioselectivity of firefly luciferase, only d-luciferin can be used as a substrate for bioluminescence reactions. Unfortunately, luciferin racemizes easily and accumulation of nonluminous l-luciferin has negative influences on the light emitting reaction. Thus, maintaining the enantiopurity
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