ChemicalBook--->CAS DataBase List--->1732-08-7

1732-08-7

1732-08-7 Structure

1732-08-7 Structure
IdentificationMore
[Name]

DIMETHYL PIMELATE
[CAS]

1732-08-7
[Synonyms]

DIMETHYL 1,7-HEPTANEDIOATE
DIMETHYL HEPTANEDIOATE
DIMETHYL HEPTANE DIONATE
DIMETHYL PIMELATE
HEPTANEDIOIC ACID,BIS-METHYL ESTER
HEPTANEDIOIC ACID DIMETHYL ESTER
PIMELIC ACID,BIS-METHYL ESTER
PIMELIC ACID DIMETHYL ESTER
Dimethyl ester of heptanedioic acid
Heptanedioic acid dimethyl
Pentane-1,5-dicarboxylic acid dimethyl ester
Pimelic acid dimethyl
[EINECS(EC#)]

217-057-4
[Molecular Formula]

C9H16O4
[MDL Number]

MFCD00008470
[Molecular Weight]

188.22
[MOL File]

1732-08-7.mol
Chemical PropertiesBack Directory
[Appearance]

Clear colorless to slightly yellow liquid
[Melting point ]

-21°C
[Boiling point ]

121-122 °C/11 mmHg (lit.)
[density ]

1.041 g/mL at 25 °C(lit.)
[vapor pressure ]

6.13Pa at 25℃
[refractive index ]

n20/D 1.431(lit.)
[Fp ]

>230 °F
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

Liquid
[color ]

Colorless to Almost colorless
[Specific Gravity]

1.041
[Water Solubility ]

Soluble in ethanol, benzene, ether. Slightly soluble in water.
[BRN ]

1777309
[LogP]

1.4 at 25℃
[CAS DataBase Reference]

1732-08-7(CAS DataBase Reference)
[EPA Substance Registry System]

Heptanedioic acid, dimethyl ester (1732-08-7)
Safety DataBack Directory
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[TSCA ]

Yes
[HS Code ]

2917.19.7050
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Methanol-->Dichloromethane-->Sodium bicarbonate-->Pimelic acid-->Cycloheptanone, 2-iodo--->Cycloheptanone, 2-nitro--->Cycloheptanone, 2-bromo-, (-)--->2-CHLOROCYCLOHEPTANONE-->1,2-PENTADIENE-->5-HEXENOIC ACID METHYL ESTER-->carbon monoxide
[Preparation Products]

Pyridine-2,6-dicarboxylic acid-->METHYL VALERATE-->Dimethyl adipate
Hazard InformationBack Directory
[Description]

Dimethyl pimelate (DMP) is valued as an important intermediate in pharmaceuticals, perfumes, lubricants, and other organic compounds. It was usually obtained by esterification from pimelic acid with alcohols[1].
[Chemical Properties]

Clear colorless to slightly yellow liquid
[Uses]

Dimethyl pimelate was used as the internal standard in the analysis of phthalates, sebacates, epoxidized soybean oil (ESBO) and polyadipates after transesterification to the ethyl esters.
[Flammability and Explosibility]

Notclassified
[References]

[1] Dudu Wu*, &Zhi Chen. “Synthesis of Dimethyl Pimelate from Cyclohexanone and Dimethyl Carbonate over Solid Base Catalysts.” Industrial & Engineering Chemistry Research 48 13 (2009): 6287–6290.
Spectrum DetailBack Directory
[Spectrum Detail]

DIMETHYL PIMELATE(1732-08-7)MS
DIMETHYL PIMELATE(1732-08-7)1HNMR
DIMETHYL PIMELATE(1732-08-7)13CNMR
DIMETHYL PIMELATE(1732-08-7)IR1
DIMETHYL PIMELATE(1732-08-7)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Dimethyl pimelate, 97%(1732-08-7)
[Alfa Aesar]

Dimethyl pimelate, 99%(1732-08-7)
[Sigma Aldrich]

1732-08-7(sigmaaldrich)
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