M47604

3-Methylglutaric acid

Name: 3-Methylglutaric acid
Brand: ALDRICH
Price: 179 USD
Availability: InStock

99%

Synonym(s):

β-Methylglutaric acid, 3-Methylpentanedioic acid

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25 G

$179.00

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About This Item

Linear Formula:

CH₃CH(CH₂COOH)₂

CAS Number:

626-51-7

Molecular Weight:

146.14

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24896942

EC Number:

210-951-5

Beilstein/REAXYS Number:

1759502

MDL number:

MFCD00002727

Key Documents

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Product Name

3-Methylglutaric acid, 99%

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

assay

99%

mp

81-86 °C (lit.)

Quality Level

200

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Show Differences

1 of 4

This Item	129860	H49901	261793
Sigma-Aldrich M47604 3-Methylglutaric acid	Sigma-Aldrich 129860 2-Methylglutaric acid	Sigma-Aldrich H49901 3-Hydroxyphenylacetic acid	Sigma-Aldrich 261793 3-Benzoylbenzoic acid
assay 99%	assay 98%	assay ≥99%	assay 99%
Quality Level 200	Quality Level 100	Quality Level 100	Quality Level 100
mp 81-86 °C (lit.)	mp 80-82 °C (lit.)	mp 129-133 °C (lit.)	mp 164-166 °C (lit.)

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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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)

Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria.

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

Phenotypic heterogeneity in the syndromes of 3-methylglutaconic aciduria.

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

Urinary organic acid screening in children with developmental language delay.

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

3-Methylglutaconyl-coenzyme-A hydratase deficiency: a new case.

K M Gibson et al.

Journal of inherited metabolic disease, 15(3), 363-366 (1992-01-01)

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3-Methylglutaric acid