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Key Documents

246549

Sigma-Aldrich

Diethylmalonic acid

98%

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About This Item

Linear Formula:
(C2H5)2C(COOH)2
CAS Number:
Molecular Weight:
160.17
Beilstein:
1768554
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

Quality Level

Assay

98%

form

powder

mp

129-131 °C (lit.)

SMILES string

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

InChI

1S/C7H12O4/c1-3-7(4-2,5(8)9)6(10)11/h3-4H2,1-2H3,(H,8,9)(H,10,11)

InChI key

LTMRRSWNXVJMBA-UHFFFAOYSA-N

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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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Earle Stellwagen et al.
Biophysical journal, 84(3), 1855-1866 (2003-03-01)
The free solution mobility of a 20-bp double-stranded DNA oligomer has been measured in diethylmalonate (DM) and Tris-acetate buffers, with and without added NaCl or TrisCl. DM buffers have the advantage that the buffering ion is anionic, so the cation
W G Reifenrath et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 4(2 Pt 2), S224-S230 (1984-04-01)
The human skin grafted athymic nude mouse, pig skin grafted athymic nude mouse, hairless dog, and weanling Yorkshire pig were evaluated as models for predicting skin penetration in man. Nine radiolabeled compounds previously tested on man were applied topically (4
Roger Peró-Gascón et al.
Journal of chromatography. A, 1508, 148-157 (2017-06-18)
In this paper we describe a strategy to estimate by CE the acidity constants (pK
W G Reifenrath et al.
Journal of pharmaceutical sciences, 73(10), 1388-1392 (1984-10-01)
A shower decontamination bench model has been used to assess quantitatively the importance of several variables (water pressure and temperature, surfactant concentration in the decontamination fluid, nozzle type, and shower time) on decontamination of nontoxic chemical warfare-agent simulants diethyl malonate
D Matosiuk et al.
Acta poloniae pharmaceutica, 53(3), 209-212 (1996-05-01)
Cyclocondensation of 1,5-disubstituted 2-aminoimidazolines with diethyl malonate in the presence of sodium methanolate leading to imidazol[1,2-alpyrimidine-5,7-dion system is presented. Prevailing of 7-hydroxy-5(1H)oxo form between three possible tautomers is discussed based on spectral data. CNS activity of nine compounds is evaluated.

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