≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice 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.
α-Hydroxyhippuric acid, nonpeptidic substrate, forms complex with peptidyl-α-hydroxyglycine α-amidating lyase catalytic core.
| Pubchem Sid | 488189865 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488189865 |
| Canonical Smiles | C1=CC=C(C=C1)C(=O)NC(C(=O)O)O |
| IUPAC Name | 2-benzamido-2-hydroxyacetic acid |
| InChIKey | GCWCVCCEIQXUQU-UHFFFAOYSA-N |
| INCHI | 1S/C9H9NO4/c11-7(10-8(12)9(13)14)6-4-2-1-3-5-6/h1-5,8,12H,(H,10,11)(H,13,14) |
| Isomeric SMILES | C1=CC=C(C=C1)C(=O)NC(C(=O)O)O |
| Molecular Weight | 195.17 |
| Reaxy-Rn | 2052165 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2052165&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 |
| Class | Benzene and substituted derivatives |
| Subclass | Benzoic acids and derivatives |
| Intermediate Tree Nodes | Benzamides - Hippuric acids and derivatives |
| Direct Parent | Hippuric acids |
| Alternative Parents | N-acyl-alpha amino acids Benzoyl derivatives Alpha hydroxy acids and derivatives Secondary carboxylic acid amides Monocarboxylic acids and derivatives Carboxylic acids Alkanolamines Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Hippuric acid - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - Benzoyl - Alpha-hydroxy acid - Hydroxy acid - Carboxamide group - Secondary carboxylic acid amide - Alkanolamine - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic nitrogen compound - Organic oxide - Carbonyl group - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as hippuric acids. These are compounds containing hippuric acid, which consists of a of a benzoyl group linked to the N-terminal of a glycine. |
| External Descriptors | N-acyl-amino acid |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 C2318311 | Certificate of Analysis | Feb 27, 2023 | B299981 |
| C2318312 | Certificate of Analysis | Feb 27, 2023 | B299981 |
| C2318313 | Certificate of Analysis | Feb 27, 2023 | B299981 |
| C2318314 | Certificate of Analysis | Feb 27, 2023 | B299981 |
| C2318315 | Certificate of Analysis | Feb 27, 2023 | B299981 |
| C2318317 | Certificate of Analysis | Feb 27, 2023 | B299981 |
| Melt Point(°C) | 211 °C (dec.) (lit.) |
|---|---|
| Molecular Weight | 195.170 g/mol |
| XLogP3 | 0.200 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 3 |
| Exact Mass | 195.053 Da |
| Monoisotopic Mass | 195.053 Da |
| Topological Polar Surface Area | 86.600 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 223.000 |
| 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 |
| 1. Quansheng Ge, Yiyuan Zhu, Chengao Li, Zhijie Ju, Renren Deng. (2023) Improving dispersibility of lanthanide-doped upconversion nanoparticles for luminescence applications in medium polarity solvents. JOURNAL OF LUMINESCENCE, [PMID:] [10.1016/j.jlumin.2023.120192] |
