3-Aminobenzoic acid

3-Aminobenzoic acid[1][2]
Skeletal formula
Skeletal formula
Ball-and-stick model
Ball-and-stick model
Names
Preferred IUPAC name
3-Aminobenzoic acid
Other names
meta-Aminobenzoic acid
m-Aminobenzoic acid
MABA
3-Carboxyaniline
m-Carboxyaniline
Identifiers
CAS Number
  • 99-05-8 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:42682 checkY
ChEMBL
  • ChEMBL307782 checkY
ChemSpider
  • 7141 checkY
DrugBank
  • DB02054 checkY
ECHA InfoCard 100.002.477 Edit this at Wikidata
EC Number
  • 202-724-4
PubChem CID
  • 7419
UNII
  • G2X3B3O37U
CompTox Dashboard (EPA)
  • DTXSID3059183 Edit this at Wikidata
InChI
  • InChI=1S/C7H7NO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4H,8H2,(H,9,10) checkY
    Key: XFDUHJPVQKIXHO-UHFFFAOYSA-N checkY
  • InChI=1/C7H7NO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4H,8H2,(H,9,10)
    Key: XFDUHJPVQKIXHO-UHFFFAOYAM
  • O=C(O)c1cc(N)ccc1
Properties
Chemical formula
C7H7NO2
Molar mass 137.13598
Appearance White solid
Density 1.51 g/cm3
Melting point 178 to 180 °C (352 to 356 °F; 451 to 453 K)
Acidity (pKa)
  • 3.07 (carboxyl; H2O)
  • 4.79 (amino; H2O)[3]
Hazards
GHS labelling:
Pictograms
GHS07: Exclamation mark
Warning
Hazard statements
H302, H315, H319, H335
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Chemical compound

3-Aminobenzoic acid (also known as meta-aminobenzoic acid or MABA) is an organic compound with the molecular formula H2NC6H4CO2H. MABA is a white solid, although commercial samples are often colored. It is only slightly soluble in water. It is soluble in acetone, boiling water, hot alcohol, hot chloroform and ether. It consists of a benzene ring substituted with an amino group and a carboxylic acid.

See also

References

  1. ^ m-Carboxyaniline - Compound Summary, PubChem.
  2. ^ 3-aminobenzoic acid, Medical Subject Headings database.
  3. ^ Haynes, William M., ed. (2016). CRC Handbook of Chemistry and Physics (97th ed.). CRC Press. p. 5–89. ISBN 978-1498754286.