L-Tyrosine - Animal Free, Moligand™, ≥99%, Fermentation method , CAS No.60-18-4

CAS: 60-18-4 Cat. No.: T1521620 Formula: C₉H₁₁NO₃ Peso molecolare: 181.19 Beilstein Registry Number: 392441 Numero EC: 200-460-4

GRADE & PURITY Animal Free, Moligand™, ≥99%, Fermentation method

Synonyms

(2S)-2-amino-3-(4-hydroxyphenyl)propanoic acid | H-Tyr-OH | P-Tyrosine | L-p-Tyrosine | (S)-Tyrosine

Storage

Protected from light,Room temperature,Desiccated

Shipped In

Normal

Specifications

Sinonimi

(2S)-2-amino-3-(4-hydroxyphenyl)propanoic acid | H-Tyr-OH | P-Tyrosine | L-p-Tyrosine | (S)-Tyrosine

Specifiche e purezza

Animal Free, Moligand™, ≥99%, Fermentation method

Meccanismi biochimici e fisiologici

L-Tyrosine consists of a polar side chain and is a non-essential amino acid. It is utilized by cells to synthesize proteins that are involved in signal transduction. L-Tyrosine acts as a receiver of phosphate groups that are transferred by kinases.

Condizioni di conservazione di stoccaggio

Protected from light,Room temperature,Desiccated

Spedito in

Normal

Grado

Animal Free, Moligand™

Purezza

≥99%

Nomi e identificatori

Sorrisi canonici

C1=CC(=CC=C1CC(C(=O)O)N)O

IUPAC Name

(2S)-2-amino-3-(4-hydroxyphenyl)propanoic acid

InChIKey

OUYCCCASQSFEME-QMMMGPOBSA-N

INCHI

1S/C9H11NO3/c10-8(9(12)13)5-6-1-3-7(11)4-2-6/h1-4,8,11H,5,10H2,(H,12,13)/t8-/m0/s1

Isomeri SMILES

C1=CC(=CC=C1C[C@@H](C(=O)O)N)O

WGK Germania

1

RTECS

YP2275600

Peso molecolare

181.19

Beilstein

392441

Reaxy-Rn

515881

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=515881&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 Tyrosine 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: Tyrosine and derivatives
• Alternative Parents: Phenylalanine and derivatives Phenylpropanoic acids L-alpha-amino acids Amphetamines and derivatives Aralkylamines 1-hydroxy-2-unsubstituted benzenoids Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Tyrosine or derivatives - Phenylalanine or derivatives - 3-phenylpropanoic-acid - Alpha-amino acid - Amphetamine or derivatives - L-alpha-amino acid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxide - Organooxygen compound - Organonitrogen compound - Amine - Primary aliphatic amine - Organic nitrogen compound - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Primary amine - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as tyrosine and derivatives. These are compounds containing tyrosine or a derivative thereof resulting from reaction of tyrosine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
• External Descriptors: Common amino acids

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

• Sensibilità: Light sensitive.
• Rotazione specifica [α]: -12 ° (C=5, 1mol/L HCl)
• Punto di infiammabilità (°F): 348.8℉
• Punto di infiammabilità (°C): 176°C
• Punto di fusione (°C): >300°C
• Peso molecolare: 181.190 g/mol
• XLogP3: -2.300
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 181.074 Da
• Monoisotopic Mass: 181.074 Da
• Topological Polar Surface Area: 83.600 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 176.000
• 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: 1