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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
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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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C Chevanet et al.
Canadian journal of microbiology, 32(3), 254-258 (1986-03-01)
Bacillomycin L is produced by Bacillus subtilis NCIB 8872 in the stationary phase; it is excreted into the culture medium, without prior accumulation in the bacterial cells. The production of bacillomycin L is largely dependent on the composition of the
O Jáuregui et al.
Electrophoresis, 21(3), 611-618 (2000-03-22)
Optimum conditions for the separation of positional isomers of chlorophenols by capillary zone electrophoresis (CZE) were established. The behavior of five volatile electrolytes (L-cysteic acid, 3-amino-1-propanesulfonic acid, aminomethanesulfonic acid, diethylmalonic acid, and ammonium acetate) was compared. The best performance based
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
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
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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