3-Aminobenzamide, 98%, Thermo Scientific Chemicals
3-Aminobenzamide, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

3-Aminobenzamide, 98%, Thermo Scientific Chemicals

Have Questions?
Change viewbuttonViewtableView
Quantity:
5 g
25 g
Catalog number A10793.06
also known as A10793-06
Price (USD)/ Each
63.50
-
Add to cart
Quantity:
5 g
Request bulk or custom format
Price (USD)/ Each
63.50
Add to cart
3-Aminobenzamide, 98%, Thermo Scientific Chemicals
Catalog numberA10793.06
Price (USD)/ Each
63.50
-
Add to cart
Chemical Identifiers
CAS3544-24-9
IUPAC Name3-aminobenzamide
Molecular FormulaC7H8N2O
InChI KeyGSCPDZHWVNUUFI-UHFFFAOYSA-N
SMILESNC(=O)C1=CC=CC(N)=C1
View more
SpecificationsSpecification SheetSpecification Sheet
Melting Point (clear melt)110.0-116.0?C
Appearance (Color)Pale cream to cream to pale brown
FormPowder
Assay (Non-aqueous acid-base Titration)≥97.5 to ≤102.5%
Assay (GC)≥97.5%
3-Aminobenzamide is used as an endogenous poly-ADP-ribosyltransferase inhibitor. Through its effects on PARPs, 3-amino benzamide causes telomere shortening and stimulates angiogenesis. It displays neuroprotective, anti-necrotic effects.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
3-Aminobenzamide is used as an endogenous poly-ADP-ribosyltransferase inhibitor. Through its effects on PARPs, 3-amino benzamide causes telomere shortening and stimulates angiogenesis. It displays neuroprotective, anti-necrotic effects.

Solubility
Soluble in dimethylformamide (∼30 mg/ml), dimethyl sulfoxide (∼30 mg/ml), phosphate buffered saline (pH7.2) (∼2 mg/ml), water (25 mg/ml), and ethanol (25 mg/ml).

Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. William F. Morgan.; James E. Cleaver.3-Aminobenzamide synergistically increases sister-chromatid exchanges in cells exposed to methyl methanesulfonate but not to ultraviolet light. Mutation Research Letters. 1982, 104, (6), 361-366.
  2. Zingarelli, B.; Cuzzocrea, S.; Zsengellér, Z.; Salzman, A. L.; Szabó, C. Protection against myocardial ischemia and reperfusion injury by 3-aminobenzamide, an inhibitor of poly (ADP-ribose) synthetase. Soviet Powder Metallurgy and Metal Ceramics. 1997, 36 (2), 205-215.