66990
3-甲基戊烯二酸
purum, ≥98.0% (GC)
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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
EC Number:
210-951-5
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1759502
MDL number:
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)
存储类别
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
法规信息
新产品
此项目有
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)
3-Methylglutaconyl-CoA hydratase deficiency: a new patient with speech retardation as the leading sign.
R Ensenauer et al.
Journal of inherited metabolic disease, 23(4), 341-344 (2000-07-15)
B Hagberg et al.
Clinica chimica acta; international journal of clinical chemistry, 134(1-2), 59-67 (1983-10-31)
We studied two children who developed normally for the first 3-4 months of life and then displayed a failure-to-thrive syndrome, regression in psychomotor development, pronounced muscular hypotonia, and liver damage. At the age of about 1-2 years, optic atrophy and
What is the origin of 3-methylglutaconic acid?
R Walsh et al.
Journal of inherited metabolic disease, 22(3), 251-255 (1999-06-29)
R I Kelley et al.
The Journal of pediatrics, 119(5), 738-747 (1991-11-01)
Seven boys with an apparently X-linked syndrome of dilated cardiomyopathy, growth retardation, neutropenia, and persistently elevated urinary levels of 3-methylglutaconate, 3-methylglutarate, and 2-ethylhydracrylate were studied. The natural history of the disorder was characterized by severe or lethal cardiac disease and
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