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Seleno-L-cystine - 90%, high purity , CAS No.29621-88-3
Basic Description
Synonyms
L-Selenocystine | 29621-88-3 | Selenocystine, L- | Seleno-L-cystine | L-3,3'-Diselenodialanine | Alanine, 3,3'-diselenodi-, L- | L-Selenocystine monohydrate | (2R,2'R)-3,3'-diselanediylbis(2-aminopropanoic acid) | 261B157KR8 | 3,3'-Diselenobis[L-alanine] | C6H12N2O4Se2 | 3,3'-
Specifications & Purity
≥90%
Storage Temp
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description
Seleno-L-cystine can be used for the synthesis of:
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organic acids and derivatives
Class
Carboxylic acids and derivatives
Subclass
Amino acids, peptides, and analogues
Intermediate Tree Nodes
Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids
Direct Parent
L-alpha-amino acids
Alternative Parents
Dicarboxylic acids and derivatives Diselenides Amino acids Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic acyclic compounds
Substituents
L-alpha-amino acid - Dicarboxylic acid or derivatives - Diselenide group - Amino acid - Carboxylic acid - Amine - Hydrocarbon derivative - Organic oxygen compound - Primary amine - Organoselenium compound - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic nitrogen compound - Carbonyl group - Organic oxide - Organopnictogen compound - Aliphatic acyclic compound
Description
This compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.
External Descriptors
Not available
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Names and Identifiers
IUPAC Name
(2R)-2-amino-3-[[(2R)-2-amino-2-carboxyethyl]diselanyl]propanoic acid
INCHI
InChI=1S/C6H12N2O4Se2/c7-3(5(9)10)1-13-14-2-4(8)6(11)12/h3-4H,1-2,7-8H2,(H,9,10)(H,11,12)/t3-,4-/m0/s1
InChIKey
JULROCUWKLNBSN-IMJSIDKUSA-N
Smiles
C(C(C(=O)O)N)[Se][Se]CC(C(=O)O)N
Isomeric SMILES
C([C@@H](C(=O)O)N)[Se][Se]C[C@@H](C(=O)O)N
WGK Germany
3
RTECS
AY6032000
PubChem CID
207306
Molecular Weight
334.09
Beilstein
1969560
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Sensitivity
Heat sensitive
Specific Rotation[α]
[α]20/D −28°, c = 1 in NaOH
Melt Point(°C)
224.5-229.5 °C (lit.)
Molecular Weight
334.110 g/mol
XLogP3
Hydrogen Bond Donor Count
4
Hydrogen Bond Acceptor Count
6
Rotatable Bond Count
7
Exact Mass
335.913 Da
Monoisotopic Mass
335.913 Da
Topological Polar Surface Area
127.000 Ų
Heavy Atom Count
14
Formal Charge
0
Complexity
192.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
2
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Jianming Zhao, Ziyuan Fang, Bingxuan Wang, Jinming Li, Abudureheman Bahatibieke, Haoye Meng, Yajie Xie, Jiang Peng, Yudong Zheng.
(2024)
Dual cross-linked polyurethane-alginate biomimetic hydrogel for elastic gradient simulation in osteochondral structures: Microenvironment modulation and tissue regeneration. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,
(136215).
2.
Xiao-Xia Zhou, Quanzhi Xiao, Kena Zhang, Yan Gao, Jie Zhang, Liping Fang, Bing Yan, Fangbai Li.
(2024)
Quantitatively Tracking the Speciation and Dynamics of Selenium Nanoparticles in Rice Plants. ANALYTICAL CHEMISTRY,
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2 Citations
B2428043