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M47604

Sigma-Aldrich

3-Methylglutaric acid

99%

Synonym(s):

β-Methylglutaric acid, 3-Methylpentanedioic acid

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About This Item

Linear Formula:
CH3CH(CH2COOH)2
CAS Number:
Molecular Weight:
146.14
Beilstein:
1759502
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

mp

81-86 °C (lit.)

SMILES string

CC(CC(O)=O)CC(O)=O

InChI

1S/C6H10O4/c1-4(2-5(7)8)3-6(9)10/h4H,2-3H2,1H3,(H,7,8)(H,9,10)

InChI key

XJMMNTGIMDZPMU-UHFFFAOYSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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3-hydroxy-3-methylglutaric, 3-methylglutaconic and 3-methylglutaric acids can be non-specific indicators of metabolic disease.
J Hammond et al.
Journal of inherited metabolic disease, 7 Suppl 2, 117-118 (1984-01-01)
K M Gibson et al.
The Journal of pediatrics, 118(6), 885-890 (1991-06-01)
Combined 3-methylglutaconic and 3-methylglutaric aciduria, one of the more common urinary organic acid abnormalities, has been observed in at least three clinical syndromes. We studied an additional seven patients with 3-methylglutaconic aciduria, four of whom were best categorized as having
M Michelson et al.
Journal of inherited metabolic disease, 22(7), 815-820 (1999-10-13)
The prevalence of 3-methylglutaconic aciduria was evaluated among children with developmental language disorders. A urine specimen was obtained from 40 children referred for developmental language delay to the Tel-Aviv Child Development Center during 12/96-6/97 and from 50 age-matched controls. Urine
H Ibel et al.
European journal of pediatrics, 152(8), 665-670 (1993-08-01)
In a 4.5-month-old boy presenting with marked muscular hypotonia in the neonatal period, hepatomegaly, cardiac hypertrophy, recurrent hypoglycemia, metabolic acidosis, and secondary carnitine deficiency, there was a considerable urinary excretion of 3-methylglutaconic and 3-methylglutaric acid. Estimation of 3-methylglutaconyl-CoA hydratase, 3-hydroxy-3-methylglutaryl-CoA
What is the origin of 3-methylglutaconic acid?
R Walsh et al.
Journal of inherited metabolic disease, 22(3), 251-255 (1999-06-29)

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