N-Glycyl-L-tyrosine dihydrate - ≥98% , CAS No.39630-46-1

CAS: 39630-46-1 Cat. No.: N303646 Molecular Weight: 274.27 PubChem CID: 57349699

GRADE & PURITY ≥98%

Synonyms

L-Tyrosine, N-glycyl-, dihydrate | AKOS030573951 | CHEBI:177941 | GLYCYL-L-TYROSINE DIHYDRATE | (S)-2-(2-Aminoacetamido)-3-(4-hydroxyphenyl)propanoic acid dihydrate | L-Tyrosine, glycyl-, dihydrate | HY-W009592A | SCHEMBL7103036 | 269373P3AW | glycyl-l-ty

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice

Overview

Product Application:

Glycyl-L-Tyrosine Dihydrate is used in process for producing N-Glycyltyrosine. Glycyl-L-Tyrosine Dihydrate is the anhydrous form of Glycyl-L-tyrosine(G720108); which is used in preparation method of high quality Aspartame and Aspartame crystallization-inducing agen

Specifications

Synonyms

L-Tyrosine, N-glycyl-, dihydrate | AKOS030573951 | CHEBI:177941 | GLYCYL-L-TYROSINE DIHYDRATE | (S)-2-(2-Aminoacetamido)-3-(4-hydroxyphenyl)propanoic acid dihydrate | L-Tyrosine, glycyl-, dihydrate | HY-W009592A | SCHEMBL7103036 | 269373P3AW | glycyl-l-ty

Specifications & Purity

≥98%

Storage

Store at 2-8°C, Protected from light

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 504771572
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504771572
• Canonical Smiles: C1=CC(=CC=C1CC(C(=O)O)NC(=O)CN)O.O.O
• IUPAC Name: (2S)-2-[(2-aminoacetyl)amino]-3-(4-hydroxyphenyl)propanoic acid;dihydrate
• InChIKey: VELZBUAWAUZDLF-WWPIYYJJSA-N
• INCHI: 1S/C11H14N2O4.2H2O/c12-6-10(15)13-9(11(16)17)5-7-1-3-8(14)4-2-7;;/h1-4,9,14H,5-6,12H2,(H,13,15)(H,16,17);2*1H2/t9-;;/m0../s1
• Isomeric SMILES: C1=CC(=CC=C1C[C@@H](C(=O)O)NC(=O)CN)O.O.O
• PubChem CID: 57349699
• Molecular Weight: 274.27

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Peptides
          • Level6 Dipeptides

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Peptides
• Direct Parent: Dipeptides
• Alternative Parents: Tyrosine and derivatives Phenylalanine and derivatives N-acyl-L-alpha-amino acids Alpha amino acid amides Phenylpropanoic acids Amphetamines and derivatives 1-hydroxy-2-unsubstituted benzenoids Secondary carboxylic acid amides Amino acids Monocarboxylic acids and derivatives Carboxylic acids Carbonyl compounds Monoalkylamines Organopnictogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Alpha-dipeptide - Tyrosine or derivatives - Phenylalanine or derivatives - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - N-acyl-l-alpha-amino acid - Alpha-amino acid amide - 3-phenylpropanoic-acid - Alpha-amino acid or derivatives - Amphetamine or derivatives - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Benzenoid - Monocyclic benzene moiety - Secondary carboxylic acid amide - Amino acid - Amino acid or derivatives - Carboxamide group - Carboxylic acid - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organopnictogen compound - Primary aliphatic amine - Organic oxide - Organonitrogen compound - Carbonyl group - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Primary amine - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond.
• 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: DMSO (Slightly), Water (Slightly)
• Sensitivity: light sensitive
• Flash Point(°C): 387.5℃
• Molecular Weight: 274.270 g/mol
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 5
• Exact Mass: 274.116 Da
• Monoisotopic Mass: 274.116 Da
• Topological Polar Surface Area: 115.000 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 275.000
• 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: 3

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