Skip to Content
Merck
All Photos(4)

Documents

127671

Sigma-Aldrich

3-Aminobenzoic acid

98%

Synonym(s):

3-Aminobenzenecarboxylic acid, 3-Carboxyaniline, m-Aminobenzoic acid, Aniline-3-carboxylic acid

Sign Into View Organizational & Contract Pricing
All Photos(4)

About This Item

Linear Formula:
H2NC6H4CO2H
CAS Number:
99-05-8
Molecular Weight:
137.14
Beilstein:
471603
EC Number:
202-724-4
MDL number:
MFCD00007795
UNSPSC Code:
12352106
PubChem Substance ID:
24847793
NACRES:
NA.22

Quality Level

100

Assay

98%

reaction suitability

reaction type: solution phase peptide synthesis

mp

178-180 °C (lit.)

application(s)

peptide synthesis

SMILES string

Nc1cccc(c1)C(O)=O

InChI

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

InChI key

XFDUHJPVQKIXHO-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

302.0 °F

Flash Point(C)

150 °C

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

Customers Also Viewed

Slide 1 of 7

1 of 7

3-Aminosalicylic acid 97%

Sigma-Aldrich

255300

3-Aminosalicylic acid

3-Aminobenzyl alcohol 97%

Sigma-Aldrich

191396

3-Aminobenzyl alcohol

2,5-Dihydroxybenzoic acid 98%

Sigma-Aldrich

149357

2,5-Dihydroxybenzoic acid

Potassium chlorate anhydrous, free-flowing, Redi-Dri™, ACS reagent, ≥99%

Sigma-Aldrich

799386

Potassium chlorate

3,5-Dimethylbenzoic acid 99%

Sigma-Aldrich

D149608

3,5-Dimethylbenzoic acid

3-(Dimethylamino)benzoic acid ≥97% (HPLC)

Sigma-Aldrich

D0787

3-(Dimethylamino)benzoic acid

3,6,9-Trioxaundecanedioic acid technical, ≥70% (T)

Sigma-Aldrich

92893

3,6,9-Trioxaundecanedioic acid

Lari Lehtiö et al.
Journal of medicinal chemistry, 52(9), 3108-3111 (2009-04-10)
Poly(ADP-ribose) polymerases (PARPs) activate DNA repair mechanisms upon stress- and cytotoxin-induced DNA damage, and inhibition of PARP activity is a lead in cancer drug therapy. We present a structural and functional analysis of the PARP domain of human PARP-3 in
Mark Eisenberg et al.
Science (New York, N.Y.), 301(5636), 1102-1104 (2003-08-23)
In memory consolidation, the memory trace stabilizes and becomes resistant to certain amnesic agents. The textbook account is that for any memorized item, consolidation starts and ends just once. However, evidence has accumulated that upon activation in retrieval, the trace
M Nagao et al.
Environmental health perspectives, 93, 169-174 (1991-06-01)
A poly(ADP-ribose) polymerase inhibitor, benzamide (BA), was found to induce flat revertants of NIH 3T3 cells that had been transformed by human Ha-ras, rat Ki-ras, rat c-raf, and human ret-II. These genes had been amplified in original transformants, but they
Satoru Kamoda et al.
Journal of chromatography. A, 1050(2), 211-216 (2004-10-29)
Carbohydrate chains in glycoprotein pharmaceuticals have important roles for the expression of their biological activities. Therefore, development of an assessment method for the carbohydrate chains is an important parameter for quality control of glycoprotein pharmaceuticals such as newly developed therapeutic
Seok Min Yoon et al.
Langmuir : the ACS journal of surfaces and colloids, 23(23), 11875-11882 (2007-10-09)
One-dimensional (1D) helical organic nanostructures were synthesized by a modified vapor-solid (VS) process, called the vaporization-condensation-recrystallization (VCR) process. The conventional solution-phase synthetic methods generally mediate self-assemblies of repeating unit molecules. To provide enough intermolecular interaction forces among the unit molecules
View All Related Papers

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