Skip to Content
Merck
All Photos(3)

Documents

A9878

Sigma-Aldrich

4-Aminobenzoic acid

≥99%, for peptide synthesis, ReagentPlus®

Synonym(s):

para-Aminobenzoic acid, PABA, Vitamin Bx, Vitamin H1

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
H2NC6H4CO2H
CAS Number:
Molecular Weight:
137.14
Beilstein:
471605
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22

product name

4-Aminobenzoic acid, ReagentPlus®, ≥99%

biological source

synthetic (organic)

Quality Level

product line

ReagentPlus®

Assay

≥99%

form

powder

reaction suitability

reaction type: solution phase peptide synthesis

mp

187-189 °C (lit.)

solubility

ethanol: 50 mg/mL, clear, colorless to faintly yellow

density

1.374 g/mL at 25 °C (lit.)

application(s)

peptide synthesis

storage temp.

2-8°C

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)

InChI key

ALYNCZNDIQEVRV-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

4-Aminobenzoic acid, also known as para-aminobenzoic acid (PABA), is utilized as a precursor in the synthesis of aromatic amines and azo dyes.

Application

4-Aminobenzoic acid is used:
  • As a building block in the synthesis of Polyamides
  • As a substrate in folic acid production
  • In the synthesis of Schiff base
  • As an organic ligand in metal-organic framework (MOFs) synthesis

Legal Information

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

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Chronic 3

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

339.8 °F - closed cup

Flash Point(C)

171 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Regioselective, photochemical bromination of aromatic compounds using N-bromosuccinimide.
Chhattise PK, et al.
Tetrahedron Letters, 49(1), 189-194 (2008)
Simple conversion of aromatic amines into azides
Q Liu
Organic Letters, 5, 2571-2572 (2003)
Unsaturated polyamides prepared from 3-amino-or 4-carboxycinnamic acid and their heat curing to thermally stable resins
CD Diakoumakos
Polymer, 36, 387-392 (1995)
Enhanced CO2 adsorption performance on amino-defective UiO-66 with 4-amino benzoic acid as the defective linker
TK Vo, et al.
Separation and Purification Technology, 274, 119079-119079 (2021)
Electropolymerized 4-aminobenzoic acid based voltammetric sensor for the simultaneous determination of food azo dyes
G Ziyatdinova
Polymers, 14, 5429-5429 (2022)

Articles

Explore folic acid importance in serum-free eukaryotic cell cultures, including CHO cells, and its role in media supplementation.

Explore folic acid importance in serum-free eukaryotic cell cultures, including CHO cells, and its role in media supplementation.

Explore folic acid importance in serum-free eukaryotic cell cultures, including CHO cells, and its role in media supplementation.

Explore folic acid importance in serum-free eukaryotic cell cultures, including CHO cells, and its role in media supplementation.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service