≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504764757 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504764757 |
| Sonrisas canónicas | C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)N4C=C(N=C4)CC(C(=O)O)N |
| IUPAC Name | (2S)-2-amino-3-(1-tritylimidazol-4-yl)propanoic acid |
| InChIKey | BSZQZNOAYQCQFZ-QHCPKHFHSA-N |
| INCHI | 1S/C25H23N3O2/c26-23(24(29)30)16-22-17-28(18-27-22)25(19-10-4-1-5-11-19,20-12-6-2-7-13-20)21-14-8-3-9-15-21/h1-15,17-18,23H,16,26H2,(H,29,30)/t23-/m0/s1 |
| Isómeros SMILES | C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)N4C=C(N=C4)C[C@@H](C(=O)O)N |
| Peso molecular | 397.47 |
| Beilstein | 767244 |
| Reaxy-Rn | 10579692 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=10579692&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 | Benzenoids |
| Clase | Triphenyl compounds |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Triphenyl compounds |
| Alternative Parents | Histidine and derivatives L-alpha-amino acids Imidazolyl carboxylic acids and derivatives Aralkylamines Benzene and substituted derivatives N-substituted imidazoles Heteroaromatic compounds Quaternary ammonium salts Carboxylic acid salts Carboxylic acids Monocarboxylic acids and derivatives Azacyclic compounds Monoalkylamines Organic oxides Organic salts Hydrocarbon derivatives Organic zwitterions Carbonyl compounds |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Triphenyl compound - Histidine or derivatives - Alpha-amino acid - Alpha-amino acid or derivatives - L-alpha-amino acid - Imidazolyl carboxylic acid derivative - Aralkylamine - Monocyclic benzene moiety - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Quaternary ammonium salt - Carboxylic acid salt - Carboxylic acid derivative - Azacycle - Carboxylic acid - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic salt - Amine - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Primary aliphatic amine - Organic oxide - Organic zwitterion - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as triphenyl compounds. These are aromatic compounds containing a triphenyl moiety. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 F2609469 | Certificate of Analysis | May 12, 2026 | H133813 |
| F2609471 | Certificate of Analysis | May 12, 2026 | H133813 |
| F2618044 | Certificate of Analysis | May 12, 2026 | H133813 |
| F2618050 | Certificate of Analysis | May 12, 2026 | H133813 |
| C2623492 | Certificate of Analysis | Mar 24, 2026 | H133813 |
| B1928105 | Certificate of Analysis | Jan 19, 2026 | H133813 |
| J2327251 | Certificate of Analysis | Aug 11, 2025 | H133813 |
| C2520270 | Certificate of Analysis | Mar 21, 2025 | H133813 |
| K2102206 | Certificate of Analysis | Aug 04, 2023 | H133813 |
| K2102208 | Certificate of Analysis | Aug 04, 2023 | H133813 |
| K2102207 | Certificate of Analysis | Aug 04, 2023 | H133813 |
| K2102210 | Certificate of Analysis | Aug 04, 2023 | H133813 |
| Punto de fusión (°C) | 210°C |
|---|---|
| Peso molecular | 397.500 g/mol |
| XLogP3 | 1.500 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 7 |
| Exact Mass | 397.179 Da |
| Monoisotopic Mass | 397.179 Da |
| Topological Polar Surface Area | 81.100 Ų |
| Heavy Atom Count | 30 |
| Formal Charge | 0 |
| Complexity | 505.000 |
| 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. Zhanpeng Ren, Jianying Wang, Chenglong Xue, Minghua Deng, Haiyang Yu, Tianci Lin, Jiayuan Zheng, Rongxiang He, Xianbao Wang, Jinhua Li. (2023) Ultrahighly Sensitive and Selective Glutathione Sensor Based on Carbon Dot-Functionalized Solution-Gate Graphene Transistor. ANALYTICAL CHEMISTRY, [PMID:37971943] [10.1021/acs.analchem.3c03656] |
| 2. Zihao Wang, Jinxiang Yang, Wei Xiao, Tianyou Chen, Changfeng Yi, Zushun Xu. (2022) Engineering of polystyrene-supported artificial catalytic triad constructed by nanoprecipitation for efficient ester hydrolysis in water. COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, [PMID:] [10.1016/j.colsurfa.2022.128902] |
