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Merck
모든 사진(1)

주요 문서

375721

Sigma-Aldrich

2-Methyl-1,3-propanediol

99%

동의어(들):

1,3-Dihydroxy-2-methylpropane, 2-Methylpropan-1,3-diol, Methylpropanediol

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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

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)


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문서 라이브러리 방문

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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