CAS 99-05-8
:3-Aminobenzoic acid
Description:
3-Aminobenzoic acid, also known as meta-aminobenzoic acid, is an aromatic amine and a derivative of benzoic acid. It features an amino group (-NH2) attached to the meta position of the benzene ring relative to the carboxylic acid group (-COOH). This compound is a white crystalline solid that is soluble in water and organic solvents, such as ethanol and acetone. It has a melting point that typically falls within a specific range, indicating its solid state at room temperature. 3-Aminobenzoic acid is known for its role in various applications, including as a precursor in the synthesis of dyes, pharmaceuticals, and as a UV filter in sunscreens. Additionally, it can act as a pH indicator and is utilized in biochemical research. The compound exhibits both acidic and basic properties due to the presence of the carboxylic acid and amino groups, respectively, allowing it to participate in various chemical reactions. Safety data indicates that it should be handled with care, as it may cause irritation upon contact with skin or eyes.
Formula:C7H7NO2
InChI:InChI=1/C7H7NO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4H,8H2,(H,9,10)/p-1
InChI key:InChIKey=XFDUHJPVQKIXHO-UHFFFAOYSA-N
SMILES:C(O)(=O)C1=CC(N)=CC=C1
Synonyms:- 3-Aminobenzenecarboxylic acid
- 3-Aminobenzoate
- 3-Aminobenzoesaeure
- 3-Aminobenzoesaure
- 3-Carboxyaniline
- Acide 3-aminobenzoique
- Acido 3-Aminobenzoico
- Aminobenzoic acid, 3-
- Aniline-3-carboxylic acid
- Benzoic Acid, M-Amino-
- Benzoic acid, 3-amino-
- M-amino benzoic acid
- Nsc 15012
- m-Aminobenzoic acid
- m-Anthranilic acid
- m-Carboxyaniline
- m-Carboxyphenylamine
- 3-Aminobenzoic acid
- AKOS BBS-00004300
- 3-aminobenzoic
- AMINOBENZOIC-3 ACID
- RARECHEM AL BO 0235
- Maba
- 1-AMINO-3-CARBOXYBENZENE
- H-M-ABZ-OH
- H-3-ABZ-OH
- 3-amino-benzoicaci
- Benzoicacid,3-amino-
- aniline-3-carboxylicacid
- m-amino-benzoicaci
- See more synonyms
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Found 14 products.
3-Aminobenzoic acid, 98%
CAS:<p>It finds its application as crystalline Intermediate for azo dyes, pharmaceuticals, and X-ray contrast media. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original A</p>Formula:C7H7NO2Purity:98%Color and Shape:Pale cream to cream, PowderMolecular weight:137.143-Aminobenzoic acid
CAS:Formula:C7H7NO2Purity:≥ 98.0%Color and Shape:White to off-white crystalline powderMolecular weight:137.14Mesalazine (Mesalamine) EP Impurity D
CAS:Formula:C7H7NO2Color and Shape:Off-White SolidMolecular weight:137.143-Aminobenzoic-2,4,5,6-d4 Acid
CAS:Formula:H2NC6D4COOHPurity:99 atom % DColor and Shape:Off White To Brown SolidMolecular weight:141.072793-Aminobenzoic Acid
CAS:Formula:C7H7NO2Purity:>99.0%(T)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:137.143-Aminobenzoic Acid
CAS:Controlled Product<p>Impurity Mesalazine EP Impurity D<br>Applications 3-Aminobenzoic Acid, is a chemoattractants against Pseudomonas strains. A reactant used in the preparation of influenza neuraminidase inhibitors, inhibitors of transthyretin amyloid fibril formation and inhibitors of the protein chaperone Hsp90.<br>References Menzella, H. et al.: J. Med. Chem., 52, 1518 (2009); Johnson, S. et al.: J. Med. Chem., 48, 1576 (2005); Parales, R.: App. Environ. Microbiol., 70, 285 (2004);<br></p>Formula:C7H7NO2Color and Shape:White To BeigeMolecular weight:137.14m-Aminobenzoic Acid pure, 98%
CAS:Formula:C7H7NO2Purity:min 98%Color and Shape:White to Brown, Crystalline powder, Clear, Pale yellowMolecular weight:137.14m-Aminobenzoic Acid extrapure AR, 99%
CAS:Formula:C7H7NO2Purity:min. 99%Color and Shape:White to Brown, Crystalline powder, ClearMolecular weight:137.143-Aminobenzoic acid
CAS:Formula:C7H7NO2Purity:97%Color and Shape:Solid, Cream coloured powderMolecular weight:137.1383-Aminobenzoic acid
CAS:<p>3-Aminobenzoic acid is a cyclic peptide that has been shown to inhibit nitrite ion formation in the human body. Nitrite ions are produced from nitric oxide and bind to hemoglobin, forming methemoglobin. 3-Aminobenzoic acid does not have a direct effect on nitric oxide, but it inhibits the conversion of nitrite ions to nitrate ions by reacting with the hemoglobin in blood. This prevents methemoglobin from being formed and reduces the risk of oxygen deprivation. 3-Aminobenzoic acid is synthesized by humans in response to an infection or other injury and can be found in human serum. The crystal structures of 3-aminobenzoic acid were determined by x-ray crystallography methods, which showed that this molecule forms hydrogen bonds with water molecules. These interactions stabilize its structure and allow for intramolecular hydrogen bonding interactions between its amino acids. The reaction mechanism was determined by kinetic energy</p>Formula:C7H7NO2Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:137.14 g/mol













