D168009
二甲基丙二酸
98%
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关于此项目
线性分子式:
(CH3)2C(COOH)2
化学文摘社编号:
分子量:
132.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-867-1
Beilstein/REAXYS Number:
774375
MDL number:
产品名称
二甲基丙二酸, 98%
InChI key
OREAFAJWWJHCOT-UHFFFAOYSA-N
InChI
1S/C5H8O4/c1-5(2,3(6)7)4(8)9/h1-2H3,(H,6,7)(H,8,9)
SMILES string
CC(C)(C(O)=O)C(O)=O
assay
98%
form
crystals
mp
191-193 °C (lit.)
Quality Level
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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
O Kniemeyer et al.
Applied and environmental microbiology, 65(8), 3319-3324 (1999-07-31)
The microbial capacity to degrade simple organic compounds with quaternary carbon atoms was demonstrated by enrichment and isolation of five denitrifying strains on dimethylmalonate as the sole electron donor and carbon source. Quantitative growth experiments showed a complete mineralization of
M Phillips et al.
Clinical chemistry, 38(1), 60-65 (1992-01-01)
We describe a method for the collection and microanalysis of the volatile organic compounds in human breath. A transportable apparatus supplies subjects with purified air and samples their alveolar breath; the volatile organic compounds are captured in an adsorptive trap
James R Harbridge et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 159(2), 195-206 (2002-12-17)
The effects of methyl rotation on electron spin-lattice relaxation times were examined by pulsed electron paramagnetic resonance for the major radicals in gamma-irradiated polycrystalline alpha-amino isobutyric acid, dimethyl-malonic acid, and L-valine. The dominant radical is the same in irradiated dimethyl-malonic
Elisabet Pires et al.
Physical chemistry chemical physics : PCCP, 22(42), 24351-24358 (2020-10-22)
The variation of the 31P chemical shift of triethylphosphine oxide in CDCl3 solution with a series of Brønsted acids at different molar ratios allows the determination of the value for the 1 : 1 species (δ1 : 1), which is much lower than the
P A Frey et al.
Science (New York, N.Y.), 264(5167), 1927-1930 (1994-06-24)
Spectroscopic properties of chymotrypsin and model compounds indicate that a low-barrier hydrogen bond participates in the mechanism of serine protease action. A low-barrier hydrogen bond between N delta 1 of His57 and the beta-carboxyl group of Asp102 in chymotrypsin can
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