M47604
3-甲基戊烯二酸
99%
别名:
β-Methylglutaric acid, 3-Methylpentanedioic acid
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关于此项目
线性分子式:
CH3CH(CH2COOH)2
化学文摘社编号:
分子量:
146.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-951-5
Beilstein/REAXYS Number:
1759502
MDL number:
Assay:
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%
Quality Level
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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
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
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
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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