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2-methyl-2,4-pentanediol

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EntityQ2792203· pop 12· linked from 6 articles

2-methyl-2,4-pentanediol

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Also known as Hexylene glycol, 2,4-Dihydroxy-2-methylpentane, 4-Methyl-2,4-pentanediol, 2-Methylpentane-2,4-diol, 2-Methyl pentane-2,4-diol, 2-Methyl-2,4-pentandiol, 1,3,3-trimethyl-1,3-propanediol, 1,3-dimethyl-3-hydroxybutanol

2-Methyl-2,4-pentanediol (MPD) is an organic compound with the formula (CH3)2C(OH)CH2CH(OH)CH3. This colourless liquid is a chiral diol. It is produced industrially from diacetone alcohol by hydrogenation. Total European and USA production was 15000 tonnes in 2000.

Chemical data

Formula
C6H14O2
Molecular weight
118.17 g/mol
IUPAC name
2-methylpentane-2,4-diol
SMILES
CC(CC(C)(C)O)O
InChIKey
SVTBMSDMJJWYQN-UHFFFAOYSA-N
XLogP
0.3
Polar surface area
40.5 Ų
H-bond donors
2
H-bond acceptors
2
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Subclass of
fatty alcohol
Mass
118.099
Show 13 more facts
upper flammable limit
7.4
lower flammable limit
1.3
melting point
-50
density
0.92
canonical SMILES
CC(CC(C)(C)O)O
chemical formula
C₆H₁₄O₂
NIOSH Pocket Guide ID
0328
boiling point
197.1
vapor pressure
0.05
flash point
209
ceiling exposure limit
125
Commons category
2-Methyl-2,4-pentanediol
found in taxon
Nicotiana tabacum
Sources (3)

via Wikidata · CC0

~2 min read

Encyclopedic overview

3 sections
Contents
  • Uses
  • Laboratory uses
  • References

2-Methyl-2,4-pentanediol (MPD) is an organic compound with the formula (CH3)2C(OH)CH2CH(OH)CH3. This colourless liquid is a chiral diol. It is produced industrially from diacetone alcohol by hydrogenation. Total European and USA production was 15000 tonnes in 2000.

2-Methyl-2,4-pentanediol exists as two enantiomers, (4R)-(−) and (4S)-(+). In the Protein Data Bank, the 3-letter code "MPD" refers to the (S)-(−) enantiomer, while "MRD" is used to refer to the (R)-(+) version. Commercial products labeled "MPD" are usually the racemate, also sold as and referred to as "hexylene glycol".

Excerpted from Wikipedia’s “2-methyl-2,4-pentanediol” article, available under the CC BY-SA 4.0 licence.