Identification | More | [Name]
METHYL HYDROGEN GLUTARATE | [CAS]
1501-27-5 | [Synonyms]
GLUTARIC ACID MONOMETHYL ESTER METHYL HYDROGEN GLUTARATE METHYL HYDROGEN PENTANE-1,5-DIOATE MONO-METHYL GLUTARATE MONOMETHYL PENTANE-1,5-DIOATE TIMTEC-BB SBB007943 5-Methoxy-5-oxopentanoic acid Methyl glutarate,mono Monomethyl ester of glutaric acid pentanedioicacid,monomethylester pentanedioicacidmonomethylester Glutaric acid monomethyl ester~Monomethyl glutarate~Pentanedioic acid monomethyl ester Glutamic Acid Monomethyl Ester Monomethyl glutaric acid Methyl hydrogen glutrate Glutaric acid 1-methyl ester Glutaric acid hydrogen methyl ester Pentanedioic acid 1-methyl ester Pentanedioic acid hydrogen 1-methyl ester 4-(Methoxycarbonyl)butanoic acid | [EINECS(EC#)]
216-116-1 | [Molecular Formula]
C6H10O4 | [MDL Number]
MFCD00004409 | [Molecular Weight]
146.14 | [MOL File]
1501-27-5.mol |
Safety Data | Back Directory | [Risk Statements ]
R36/38:Irritating to eyes and skin . | [Safety Statements ]
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) . S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [TSCA ]
Yes | [HS Code ]
29171900 |
Hazard Information | Back Directory | [Chemical Properties]
Clear light yellow liquid | [Uses]
It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff. | [Definition]
ChEBI: A dicarboxylic acid monoester that the monomethyl ester of glutaric acid. | [Synthesis Reference(s)]
Journal of the American Chemical Society, 107, p. 1365, 1985 DOI: 10.1021/ja00291a042 Tetrahedron, 49, p. 8465, 1993 DOI: 10.1016/S0040-4020(01)81929-3 | [Synthesis]
GENERAL METHOD: A methanol (MeOH, 150 mL) solution of potassium hydroxide (KOH, 5.87 g, 104.65 mmol) was added to dimethyl glutarate (13.15 g, 90 mmol) and the reaction mixture was stirred for 4 hours at room temperature. After completion of the reaction, the solvent was removed under reduced pressure and extracted by adding ether (Et2O, 100 mL) and water (H2O, 200 mL). The organic layer was separated, washed with saturated brine, dried over anhydrous magnesium sulfate (MgSO4) and concentrated under reduced pressure to give compound 3a as a yellow oil (4.61 g, 32% yield). The aqueous layer was acidified to pH 3 with concentrated hydrochloric acid and subsequently extracted with ether (3 x 100 mL). The organic phases were combined, washed with saturated brine (3 x 100 mL) and dried over anhydrous magnesium sulfate (MgSO4). The solvent was removed under reduced pressure to give a mixture of white solid and oil. After filtration and vacuum concentration, the compound was purified by silica gel column chromatography to give compound 4a as a colorless oil (5.79 g, 44% yield). | [IC 50]
Human Endogenous Metabolite | [References]
[1] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 12, p. 3865 - 3872 [2] Chemistry Letters, 1995, # 7, p. 539 - 540 |
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