L-Phenylalanine-d5 - ≥98 atom% D,≥98% , CAS No.56253-90-8

CAS: 56253-90-8 Cat. No.: L354493 Formula: C₉D₅H₆NO₂ Peso molecolare: 170.22

GRADE & PURITY ≥98 atom% D,≥98%

Synonyms

(2S)-2-amino-3-(2,3,4,5,6-pentadeuteriophenyl)propanoic acid | (2,3,4,5,6-2H5)-L-PHENYLALANINE | L-Phenylalanine-d5 | 2,3,4,5,6-Pentadeutero-L-phenylalanine | HY-N0215S12 | D98700 | CHEBI:192084 | DTXSID101315572 | L-(2,3,4,5,6-2H5)Phenylalanine | (2S)-2-

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice

Panoramica

Application：

Labeled L-Phenylalanine is an essential amino acid. L-Phenylalanine is biologically converted into L-tyrosine, another one of the DNA-encoded amino acids, which in turn is converted to L-DOPA and further converted into dopamine, norepinephrine, and epinephrine. L-Phenylalanine is produced for medical, feed, and nutritional applications such as in the preparation of Aspartame.

Specifications

Sinonimi

(2S)-2-amino-3-(2,3,4,5,6-pentadeuteriophenyl)propanoic acid | (2,3,4,5,6-2H5)-L-PHENYLALANINE | L-Phenylalanine-d5 | 2,3,4,5,6-Pentadeutero-L-phenylalanine | HY-N0215S12 | D98700 | CHEBI:192084 | DTXSID101315572 | L-(2,3,4,5,6-2H5)Phenylalanine | (2S)-2-

Specifiche e purezza

≥98 atom% D,≥98%

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Protected from light

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Tipo di azione

ANTAGONIST

Purezza

≥98 atom% D,≥98%

Nomi e identificatori

Pubchem Sid

504767306

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504767306

Sorrisi canonici

C1=CC=C(C=C1)CC(C(=O)O)N

IUPAC Name

(2S)-2-amino-3-(2,3,4,5,6-pentadeuteriophenyl)propanoic acid

InChIKey

COLNVLDHVKWLRT-HRVDQBBZSA-N

INCHI

1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)/t8-/m0/s1/i1D,2D,3D,4D,5D

Isomeri SMILES

[2H]C1=C(C(=C(C(=C1[2H])[2H])C[C@@H](C(=O)O)N)[2H])[2H]

CAS alternativo

63-91-2（unlabelled）

Peso molecolare

170.22

Reaxy-Rn

1910407

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1910407&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives
• Direct Parent: Phenylalanine and derivatives
• Alternative Parents: Phenylpropanoic acids L-alpha-amino acids Amphetamines and derivatives Aralkylamines Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenylalanine or derivatives - 3-phenylpropanoic-acid - Alpha-amino acid - Amphetamine or derivatives - L-alpha-amino acid - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Primary amine - Primary aliphatic amine - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Amine - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as phenylalanine and derivatives. These are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine 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

Proprietà chimiche e fisiche

• Solubilità: DMSO (Slightly), Water (Slightly)
• Sensibilità: Moisture sensitive；Light sensitive
• Punto di fusione (°C): 243-246° C
• Peso molecolare: 170.220 g/mol
• XLogP3: -1.500
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 170.11 Da
• Monoisotopic Mass: 170.11 Da
• Topological Polar Surface Area: 63.300 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 153.000
• Isotope Atom Count: 5
• 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: 1

Domande frequenti

What is the purity of this product?

This product is isotopically enriched to ≥98 atom% deuterium. Isotopic enrichment is a separate specification from chemical purity — a labelled compound has both. This product is supplied at ≥98% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at 2–8 °C, protected from light. The material is light-sensitive — keep it in its original opaque or amber container.

How is this product shipped?

This product ships chilled on wet ice. Unpack on arrival and transfer it to the storage condition stated above.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 56253-90-8, the molecular formula is C9D5H6NO2, and the molecular weight is 170.22 g/mol. InChIKey COLNVLDHVKWLRT-HRVDQBBZSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.