3-Aminobenzoic acid 98% | Sigma-Aldrich

Properties

Related Categories	Aromatic Amino Acids, Chemical Biology, Chemical Synthesis, Peptide Chemistry, Unnatural Amino Acid Derivatives More...
assay	98%
mp	178-180 °C(lit.)

Description

Packaging

25, 100, 500 g in glass bottle

Price and Availability

Chemical Biology Portfolio

Sigma-Aldrich has an ever expanding
portfolio of Chemical Biology products,
which incorporate techniques and strengths
of chemistry to address fundamentally important questions in biology, medicine,
and drug discovery.

view Products

Suggested Laboratory Gloves

This substance has been tested against several types of hand protection for CE compliance. Click below to find the recommended gloves for handling this product.

for splash & immersion protection

Related Papers

Synthesis and evaluation of novel aromatic substrates and competitive inhibitors of GABA aminotransferase. Michael D Clift et al Bioorg. Med. Chem. Lett. 18, 3122-5, (2008)

Documents

Certificate of Analysis

Certificate of Origin

FT-IR Condensed Phase

FT-IR Raman

FT-NMR

Safety Information

Symbol	GHS07
Signal word	Warning
Hazard statements	H302-H315-H319-H335
Precautionary statements	P261-P305 + P351 + P338
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes (Europe)	Xn
Risk Statements (Europe)	22-36/37/38
Safety Statements (Europe)	26
WGK Germany	2
RTECS	DG1225000
Flash Point(F)	302 °F
Flash Point(C)	150 °C

Technical information & documentation associated with this product is available in the Safety & Documentation tab.

Papers

Set your institution to view full text papers.

Synthesis and evaluation of novel aromatic substrates and competitive inhibitors of GABA aminotransferase. Michael D Clift et al Bioorg. Med. Chem. Lett. 18, 3122-5, (2008)

Loading...

Structural basis for inhibitor specificity in human poly(ADP-ribose) polymerase-3. Lari Lehtiö et al J. Med. Chem. 52, 3108-11, (2009)

Loading...

Three-dimensional quantitative structure-activity relationship analyses of substrates of the human proton-coupled amino acid transporter 1 (hPAT1). Iris Thondorf et al Bioorg. Med. Chem. 19, 6409-18, (2011)

Loading...

Merck 14,421

Beil. 14,IV,1092

Aldrich MSDS 1, 60:A / Corp MSDS 1 (1), 138:A / FT-IR 1 (2), 192:C / FT-IR 2 (2), 2656:A / FT-NMR 1 (2), 1071:B / IR-Spectra (3), 959:H / IR-Spectra (2), 840:D / NMR-Reference 2 (2), 189:D / RegBook 1 (2), 1787:E / Sax 6, 194 / Sigma FT-IR 1 (2), 256:B / Structure Index 1, 285:C:4