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127671

Sigma-Aldrich

3-Aminobenzoic acid

98%, for peptide synthesis

Synonym(s):

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

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25 G
PLN 158.00
100 G
PLN 194.00
500 G
PLN 628.00

PLN 158.00


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25 G
PLN 158.00
100 G
PLN 194.00
500 G
PLN 628.00

About This Item

Linear Formula:
H2NC6H4CO2H
CAS Number:
Molecular Weight:
137.14
Beilstein:
471603
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22

PLN 158.00


Please contact Customer Service for Availability

Request a Bulk Order

Product Name

3-Aminobenzoic acid, 98%

Quality Level

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

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Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

302.0 °F - closed cup

Flash Point(C)

150 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
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
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 Wakselman et al.
Journal of medicinal chemistry, 36(11), 1539-1547 (1993-05-28)
In order to obtain selective suicide substrates of trypsin-like proteases including plasminogen activators, plasmin, and thrombin, a series of cyclopeptides cyclo[Arg or Lys-aB(CH2X)-Gly4], in which a substituted o- or m-aminobenzoyl group constitutes a latent electrophile, have been prepared. Treatment of
Khaled H Almabruk et al.
Organic letters, 15(7), 1678-1681 (2013-03-26)
A mutasynthetic strategy has been used to generate fluorinated TM-025 and TM-026, two biosynthetically engineered pactamycin analogues produced by Streptomyces pactum ATCC 27456. The fluorinated compounds maintain excellent activity and selectivity toward chloroquine-sensitive and multidrug-resistant strains of malarial parasites as

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