≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504753962 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504753962 |
| Sonrisas canónicas | C1=CC(=C(C=C1CC(C(=O)O)N)[N+](=O)[O-])O |
| IUPAC Name | (2S)-2-amino-3-(4-hydroxy-3-nitrophenyl)propanoic acid |
| InChIKey | FBTSQILOGYXGMD-LURJTMIESA-N |
| INCHI | 1S/C9H10N2O5/c10-6(9(13)14)3-5-1-2-8(12)7(4-5)11(15)16/h1-2,4,6,12H,3,10H2,(H,13,14)/t6-/m0/s1 |
| Isómeros SMILES | C1=CC(=C(C=C1C[C@@H](C(=O)O)N)[N+](=O)[O-])O |
| WGK Alemania | 3 |
| Peso molecular | 226.19 |
| Beilstein | 2813157 |
| Reaxy-Rn | 2219127 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2219127&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Clase | 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 L-alpha-amino acids Nitrophenols Nitrobenzenes Nitroaromatic compounds 1-hydroxy-2-unsubstituted benzenoids Aralkylamines Amino acids Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Carboxylic acids Monocarboxylic acids and derivatives Organic zwitterions Carbonyl compounds Hydrocarbon derivatives Organic oxides Monoalkylamines Organopnictogen compounds |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Tyrosine or derivatives - Phenylalanine or derivatives - 3-phenylpropanoic-acid - Alpha-amino acid - Amphetamine or derivatives - Nitrophenol - L-alpha-amino acid - Nitrobenzene - Nitroaromatic compound - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Monocyclic benzene moiety - Benzenoid - C-nitro compound - Amino acid - Organic nitro compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxoazanium - Organic zwitterion - Organonitrogen compound - Amine - Organic oxide - Organic nitrogen compound - Organooxygen compound - Primary aliphatic amine - Hydrocarbon derivative - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Primary amine - Aromatic homomonocyclic compound |
| Descripción | 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 | non-proteinogenic L-alpha-amino acid - L-tyrosine derivative - 3-nitrotyrosine |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 L2518080 | Certificate of Analysis | Dec 24, 2025 | N111009 |
| A2622011 | Certificate of Analysis | Feb 10, 2025 | N111009 |
| B2506102 | Certificate of Analysis | Feb 10, 2025 | N111009 |
| B2506103 | Certificate of Analysis | Dec 09, 2024 | N111009 |
| C2116211 | Certificate of Analysis | Dec 09, 2024 | N111009 |
| C2116212 | Certificate of Analysis | Dec 09, 2024 | N111009 |
| C2116214 | Certificate of Analysis | Dec 09, 2024 | N111009 |
| C2116215 | Certificate of Analysis | Dec 09, 2024 | N111009 |
| Solubilidad | Soluble in water (partly miscible), 1N hydrochloric acid (50 mg/ml), acidic aqueous solution , ethanol, DMSO, DMF and PBS (pH 7.2) (~2 mg/ml). |
|---|---|
| Rotación específica [α] | 3° (C=1,1mol/L HCl) |
| Punto de fusión (°C) | 233-235°C |
| Peso molecular | 226.190 g/mol |
| XLogP3 | -2.000 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 3 |
| Exact Mass | 226.059 Da |
| Monoisotopic Mass | 226.059 Da |
| Topological Polar Surface Area | 129.000 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 278.000 |
| 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 |
| 1. Huifang Wu, Qiqi Wang, Lingfeng Zhu, Xinyue Liu, Lizhong Liu, Changlun Tong. (2025) Time-Resolved Phosphorescence and Colorimetric Assays of Diabetes Biomarkers: Simultaneous Detection of 3-Nitro-l-Tyrosine and Total Antioxidant Capacity via Zeolite-Confined Carbon Dots. ANALYTICAL CHEMISTRY, [PMID:41163475] [10.1021/acs.analchem.5c05306] |
