D6796
meso-2,3-Diaminosuccinic acid
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About This Item
Empirical Formula (Hill Notation):
C4H8N2O4
CAS Number:
Molecular Weight:
148.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
245-500-1
MDL number:
InChI key
PGNYNCTUBKSHHL-XIXRPRMCSA-N
InChI
1S/C4H8N2O4/c5-1(3(7)8)2(6)4(9)10/h1-2H,5-6H2,(H,7,8)(H,9,10)/t1-,2+
SMILES string
NC(C(N)C(O)=O)C(O)=O
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
color
white
application(s)
peptide synthesis
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Kirsten Zeitler et al.
The Journal of organic chemistry, 69(18), 6134-6136 (2004-09-18)
Homogeneous, Rh-catalyzed hydrogenation of heteromeric olefinic glycine dimers presents an efficient route to diastereomerically pure, orthogonally protected diaminosuccinic acid derivatives depending on the double bond geometry of the starting material. The products were obtained as racemates.
A Rinaldi et al.
European journal of biochemistry, 117(3), 635-638 (1981-07-01)
meso-Diaminosuccinic acid, a natural antagonist of aspartic acid, is a good substrate for beef kidney D-aspartate oxidase. The oxygen consumption and the ammonia production are in good agreement with the stoichiometry of a typical oxidative deamination. The deamination involves only
C Riemer et al.
The journal of peptide research : official journal of the American Peptide Society, 63(3), 196-199 (2004-03-31)
The stereoselective synthesis of orthogonally protected 3-azido aspartic acid derivatives is described. The convenience of their application as 2,3-diaminosuccinic acid in peptide chemistry was demonstrated by the incorporation of the nonproteinogenic diamino diacid as a cystine-substitute into the core structure
J E Turner et al.
Basic life sciences, 63, 155-166 (1994-01-01)
Detailed Monte Carlo calculations provide a powerful tool for understanding mechanisms of radiation damage to biological molecules irradiated in aqueous solution. This paper describes the computer codes, OREC and RADLYS, which have been developed for this purpose over a number
Yoshito Kawasaki et al.
Journal of chromatography. A, 1160(1-2), 246-253 (2007-06-08)
The advanced Marfey's method consists of a chromatography technique for the separation of amino acids into each enantiomer by derivatization with 1-fluoro-2,4-dinitrophenyl-5-L-leucinamide (L-FDLA), and a detection method using liquid chromatography/mass spectrometry (LC/MS) which can determine the non-empirically the absolute configuration
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