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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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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

product name

3-Aminobenzoic acid, 98%

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

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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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Certificates of Analysis (COA)

Lot/Batch Number
00228BJ
08404EE
06423AE
01816KD
07818ED

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Science (New York, N.Y.), 301(5636), 1102-1104 (2003-08-23)
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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
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