≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Argon charged,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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Phthalamic acid can be synthesized from the reaction between ammonia and phthalic anhydride by a modified Auger′s method. Kinetic studies of the intramolecular carboxylic-group assisted hydrolysis of amide bond of phthalamic acid provided the value of pseudo-first order rate constant (kobs) as 5.1×10-5sec-1 at pH 1.3-1.8 and 35°C. It undergoes hydrolysis about 105 times faster than benzamide.
| Pubchem Sid | 488180222 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488180222 |
| Kanonisches Lächeln | C1=CC=C(C(=C1)C(=O)N)C(=O)O |
| IUPAC Name | 2-carbamoylbenzoic acid |
| InChIKey | CYMRPDYINXWJFU-UHFFFAOYSA-N |
| INCHI | 1S/C8H7NO3/c9-7(10)5-3-1-2-4-6(5)8(11)12/h1-4H,(H2,9,10)(H,11,12) |
| Isomere SMILES | C1=CC=C(C(=C1)C(=O)N)C(=O)O |
| WGK Deutschland | 3 |
| PubChem CID | 6957 |
| Molekulargewicht | 165.15 |
| Beilstein | 9(3)4191 |
| Reaxy-Rn | 1868205 |
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 |
| Klasse | Benzene and substituted derivatives |
| Subclass | Benzoic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzoic acids |
| Alternative Parents | Benzoyl derivatives Monocarboxylic acids and derivatives Carboxylic acids Carboximidic acids Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Benzoic acid - Benzoyl - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Carboximidic acid derivative - Carboximidic acid - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic homomonocyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as benzoic acids. These are organic Compounds containing a benzene ring which bears at least one carboxyl group. |
| External Descriptors | carbamoylbenzoic acid |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Datum | Artikel |
|---|---|---|---|
 E2308644 | Certificate of Analysis | Mar 08, 2023 | P160471 |
| E2308649 | Certificate of Analysis | Mar 08, 2023 | P160471 |
| E2308663 | Certificate of Analysis | Mar 08, 2023 | P160471 |
| E2308720 | Certificate of Analysis | Mar 08, 2023 | P160471 |
| E2308772 | Certificate of Analysis | Mar 08, 2023 | P160471 |
| E2308781 | Certificate of Analysis | Mar 08, 2023 | P160471 |
| E2308784 | Certificate of Analysis | Mar 08, 2023 | P160471 |
| E2308796 | Certificate of Analysis | Mar 08, 2023 | P160471 |
| Löslichkeit | Soluble in Methanol |
|---|---|
| Empfindlichkeit | Moisture sensitive |
| Schmelzpunkt (°C) | 149°C(lit.) |
| Molekulargewicht | 165.150 g/mol |
| XLogP3 | 0.100 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Exact Mass | 165.043 Da |
| Monoisotopic Mass | 165.043 Da |
| Topological Polar Surface Area | 80.400 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 202.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| 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 |
