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Merck

100536

Sigma-Aldrich

4-Aminobenzoesäure

99%, for peptide synthesis, ReagentPlus®

Synonym(e):

PABA, Vitamin H1, Vitamin Bx

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About This Item

Lineare Formel:
H2NC6H4CO2H
CAS-Nummer:
Molekulargewicht:
137.14
Beilstein:
471605
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352106
eCl@ss:
32160406
PubChem Substanz-ID:
NACRES:
NA.22

product name

4-Aminobenzoesäure, ReagentPlus®, 99%

Qualitätsniveau

Produktlinie

ReagentPlus®

Assay

99%

Form

solid

Eignung der Reaktion

reaction type: solution phase peptide synthesis

mp (Schmelzpunkt)

187-189 °C (lit.)

Löslichkeit

95% ethanol: soluble 5%, clear to slightly hazy, colorless to yellow

Dichte

1.374 g/mL at 25 °C (lit.)

Anwendung(en)

peptide synthesis

SMILES String

Nc1ccc(cc1)C(O)=O

InChI

1S/C7H7NO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,8H2,(H,9,10)

InChIKey

ALYNCZNDIQEVRV-UHFFFAOYSA-N

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Allgemeine Beschreibung

4-Aminobenzoic acid (4-ABA) acts as an bacterial cofactor and participates in the synthesis of folic acid. It is a versatile reagent for structure extension through linear hydrogen-bonding associations, involving both the carboxylic acid and amine functional groups. Formation of 4-ABA monolayer film on glassy carbon electrode (GCE) by amino cation radical method has been described. Molecular adducts of 4-ABA have been prepared and their characterization by infrared spectroscopy and X-ray diffration methods have been reported.

Anwendung

4-Aminobenzoic acid may be used in the following studies:
  • Covalent modification of glassy carbon electrode.
  • Synthesis of 1,4-(2-chlorobenzylidene)aminobenzoic acid (Schiff base).
  • Spectrophotometric determination of the trace amounts of dopamine, methyldopa and levodopa.
  • Synthesis of 1:1 proton-transfer compound with 5-sulfosalicylic acid.

Rechtliche Hinweise

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

H-Sätze

P-Sätze

Gefahreneinstufungen

Aquatic Chronic 3

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

339.8 °F - closed cup

Flammpunkt (°C)

171 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Die Dokumentenbibliothek aufrufen

Layer-by-layer assembly of multilayer films consisting of silicotungstate and a cationic redox polymer on 4-aminobenzoic acid modified glassy carbon electrode and their electrocatalytic effects.
Cheng L, et al.
Analytica Chimica Acta, 34(12), 1093-1100 (1999)
Gehad G Mohamed et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 62(4-5), 1140-1150 (2005-06-16)
Metal complexes of Schiff base derived from 2-thiophene carboxaldehyde and 2-aminobenzoic acid (HL) are reported and characterized based on elemental analyses, IR, 1H NMR, solid reflectance, magnetic moment, molar conductance and thermal analysis (TGA). The ligand dissociation as well as
The 1: 1 proton-transfer compound of 5-sulfosalicylic acid with 4-aminobenzoic acid.
Smith G, et al.
Acta Crystallographica Section E, Structure Reports Online, 61(2), 313-316 (2005)
Spectrophotometric determination of catecholamines based on their oxidation reaction followed by coupling with 4-aminobenzoic acid.
Madrakian T, et al.
Journal of the Brazilian Chemical Society, 17(7), 1259-1265 (2006)
Covalent modification of a glassy carbon surface by 4-aminobenzoic acid and its application in fabrication of a polyoxometalates-consisting monolayer and multilayer films.
Liu J, et al.
Langmuir, 16(19), 7471-7476 (2000)

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