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D168009

Sigma-Aldrich

Dimethylmalonic acid

98%

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About This Item

Linear Formula:
(CH3)2C(COOH)2
CAS Number:
595-46-0
Molecular Weight:
132.11
Beilstein:
774375
EC Number:
209-867-1
MDL number:
MFCD00004193
UNSPSC Code:
12352100
PubChem Substance ID:
24893513
NACRES:
NA.22

Quality Level

200

Assay

98%

form

crystals

mp

191-193 °C (lit.)

SMILES string

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

InChI

1S/C5H8O4/c1-5(2,3(6)7)4(8)9/h1-2H3,(H,6,7)(H,8,9)

InChI key

OREAFAJWWJHCOT-UHFFFAOYSA-N

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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL5143
BCCM1790
BCCK4039
BCCJ3498
BCCG6223

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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
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
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
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
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
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