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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque DL-Tyrosine - ≥98% , CAS No.556-03-6
Disponível para encomenda
Synonyms
(DL)-Tyrosine | 2-amino-3-(4-hydroxyphenyl)propanoic acid | 2-amino-3-(4-hydroxyphenyl)-propanoic acid | AI3-18479 | (2s)-tyrosine | Pharmakon1600-01300046 | SY014304 | DL-Tyrozine | DTXSID50859040 | (.+-.)-Tyrosine | DL-Tyrosine, puriss., >=99.0% (NT) |
Storage
Protected from light,Room temperature
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Protected from light,Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 10 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
(DL)-Tyrosine | 2-amino-3-(4-hydroxyphenyl)propanoic acid | 2-amino-3-(4-hydroxyphenyl)-propanoic acid | AI3-18479 | (2s)-tyrosine | Pharmakon1600-01300046 | SY014304 | DL-Tyrozine | DTXSID50859040 | (.+-.)-Tyrosine | DL-Tyrosine, puriss., >=99.0% (NT) |
Especificações e pureza
≥98%
Condições de armazenamento de armazenamento
Protected from light,Room temperature
Nomes e identificadores Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488179604
Sorrisos canónicos
C1=CC(=CC=C1CC(C(=O)O)N)O
IUPAC Name
2-amino-3-(4-hydroxyphenyl)propanoic acid
InChIKey
OUYCCCASQSFEME-UHFFFAOYSA-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)
SMILES isoméricas
C1=CC(=CC=C1CC(C(=O)O)N)O
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=515881&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification 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 Amphetamines and derivatives Alpha amino acids 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 - Amphetamine or derivatives - Alpha-amino acid - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Phenol - Monocyclic benzene moiety - Benzenoid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxygen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Primary aliphatic amine - Organic nitrogen compound - Carbonyl group - Organic oxide - Organopnictogen compound - Amine - Aromatic homomonocyclic compound Descrição 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 alpha-amino acid - aromatic amino acid 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.
Estrutura 3D Alvos associados (não humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Sensibilidade Light sensitive. Ponto de fusão (°C) ≥300°C Peso molecular 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 0 Undefined Atom Stereocenter Count 1 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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