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Merck
CN

66990

3-Methylglutaric acid

purum, ≥98.0% (GC)

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About This Item

Linear Formula:
CH3CH(CH2COOH)2
CAS Number:
Molecular Weight:
146.14
EC Number:
210-951-5
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1759502
MDL number:
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InChI key

XJMMNTGIMDZPMU-UHFFFAOYSA-N

InChI

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

SMILES string

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

grade

purum

assay

≥98.0% (GC)

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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W Lehnert et al.
European journal of pediatrics, 143(4), 301-303 (1985-03-01)
A girl suffering from marked muscular hypotonia, severe statomotor and mental retardation, bilateral optic atrophy with chorioretinal degeneration, convulsions and a moderate compensated metabolic acidosis is described. Screening for metabolic disorders revealed massive 3-methylglutaconic with 3-methylglutaric aciduria leading to the
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)
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
Behr syndrome.
T Lerman-Sagie
Pediatric neurology, 12(1), 90-90 (1995-01-01)
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

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