L-Asparagine Monohydrate - Animal Free, for cell culture, ≥99% , CAS No.5794-13-8

CAS: 5794-13-8 Cat. No.: A119452 Molecular Weight: 150.13 Beilstein Registry Number: 1723527 EC Number: 611-593-6

GRADE & PURITY Animal Free, for Cell culture, ≥99%

Synonyms

L-Asparagine monohydrate, suitable for cell culture, BioReagent | L-Asparagine monohydrate, p.a., 98.5% | L-Asparagine, monohydrate | (2S)-2,4-diamino-4-oxobutanoic acid;hydrate | Thomaeamin | Asparagine monohydrate, European Pharmacopoeia (EP) Reference

Storage

Protected from light,Room temperature

Shipped In

Normal

Specifications

Synonyms

L-Asparagine monohydrate, suitable for cell culture, BioReagent | L-Asparagine monohydrate, p.a., 98.5% | L-Asparagine, monohydrate | (2S)-2, 4-diamino-4-oxobutanoic acid;hydrate | Thomaeamin | Asparagine monohydrate, European Pharmacopoeia (EP) Reference

Specifications & Purity

Animal Free, for cell culture, ≥99%

Biochemical and Physiological Mechanisms

L-Asparagine, a proteinogenic amino acid, is used in biomanufacturing cell culture systems for the production of therapeutic recombinant proteins and monoclonal antibodies and in cell culture based research.

Storage

Protected from light, Room temperature

Shipped In

Normal

Grade

Animal Free, for Cell culture

Purity

≥99%

Names and Identifiers

• Pubchem Sid: 504757650
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504757650
• Canonical Smiles: C(C(C(=O)O)N)C(=O)N.O
• IUPAC Name: (2S)-2,4-diamino-4-oxobutanoic acid;hydrate
• InChIKey: RBMGJIZCEWRQES-DKWTVANSSA-N
• INCHI: 1S/C4H8N2O3.H2O/c5-2(4(8)9)1-3(6)7;/h2H,1,5H2,(H2,6,7)(H,8,9);1H2/t2-;/m0./s1
• Isomeric SMILES: C([C@@H](C(=O)O)N)C(=O)N.O
• WGK Germany: 1
• Molecular Weight: 150.13
• Beilstein: 1723527
• Reaxy-Rn: 6234992
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6234992&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 Asparagine and derivatives

• 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
• Direct Parent: Asparagine and derivatives
• Alternative Parents: L-alpha-amino acids Fatty amides Fatty acids and conjugates Primary carboxylic acid amides Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Asparagine or derivatives - L-alpha-amino acid - Alpha-amino acid - Fatty acyl - Fatty acid - Fatty amide - Amino acid - Primary carboxylic acid amide - Carboxamide group - Monocarboxylic acid or derivatives - Carboxylic acid - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Carbonyl group - Amine - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as asparagine and derivatives. These are compounds containing asparagine or a derivative thereof resulting from reaction of asparagine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
• 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.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: Soluble in water.
• Specific Rotation[α]: 31 ° (C=10, HCl)
• Melt Point(°C): 233-235°C
• Molecular Weight: 150.130 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 3
• Exact Mass: 150.064 Da
• Monoisotopic Mass: 150.064 Da
• Topological Polar Surface Area: 107.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 134.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• 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: 2

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