2-AMINO-N-HYDROXY-BENZAMIDINE
- Product Name
- 2-AMINO-N-HYDROXY-BENZAMIDINE
- CAS No.
- 16348-49-5
- Chemical Name
- 2-AMINO-N-HYDROXY-BENZAMIDINE
- Synonyms
- 2-Amino benzamidoxime;2-Aminobenzamidoxime,97%;2-Aminobenzamidoxime, 97%;2-Amino-N-hydroxybenzimidamide;Benzenecarboximidamide, 2-amino-N-hydroxy-
- CBNumber
- CB8707275
- Molecular Formula
- C7H9N3O
- Formula Weight
- 151.17
- MOL File
- 16348-49-5.mol
2-AMINO-N-HYDROXY-BENZAMIDINE Property
- Melting point:
- 71-75℃
- Boiling point:
- 318.2±44.0 °C(Predicted)
- Density
- 1.34±0.1 g/cm3(Predicted)
- storage temp.
- 2-8°C
- solubility
- DMF: 5 mg/ml; DMSO: 5 mg/ml; Ethanol: 5 mg/ml; PBS (pH 7.2): 2 mg/ml
- form
- A crystalline solid
- pka
- 6.74±0.69(Predicted)
- color
- White to off-white
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P405Store locked up.
N-Bromosuccinimide Price
- Product number
- 11062
- Product name
- 2-amino Benzamidoxime
- Purity
- ≥97%
- Packaging
- 1g
- Price
- $66
- Updated
- 2024/03/01
- Product number
- 11062
- Product name
- 2-amino Benzamidoxime
- Purity
- ≥97%
- Packaging
- 5g
- Price
- $274
- Updated
- 2024/03/01
- Product number
- 11062
- Product name
- 2-amino Benzamidoxime
- Purity
- ≥97%
- Packaging
- 500mg
- Price
- $36
- Updated
- 2024/03/01
- Product number
- A577125
- Product name
- 2-AminobenzamideOxime
- Packaging
- 10mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- A577125
- Product name
- 2-AminobenzamideOxime
- Packaging
- 50mg
- Price
- $55
- Updated
- 2021/12/16
2-AMINO-N-HYDROXY-BENZAMIDINE Chemical Properties,Usage,Production
Uses
2-Amino benzamidoxime (ABAO compound 6) can react quickly with aldehydes to form stable 1, 2-dihydroquinazoline 3-oxides in aqueous solutions. The 2-Amino benzamidoxime reaction process consists of the formation of a Schiff base as a rate-determining step, followed by rapid intramolecular cyclization. The reaction rate is dependent on pH, indicating that protonated benzamidoxime is involved in the formation of Schiff bases as an internal generalized acid. Substituents on the aromatic ring can increase the alkalinity of the aromatic amine, thus speeding up the reaction. The reactive properties of 2-Amino benzamidoxime make it a potential platform for the development of new bioconjugated strategies, fluorescent probes, and post-translational diversification of genetic coding libraries[1].
References
[1] Kitov P I, et al. Rapid, hydrolytically stable modification of aldehyde-terminated proteins and phage libraries[J]. Journal of the American Chemical Society, 2014, 136(23): 8149-8152. DOI:10.1021/ja5023909
2-AMINO-N-HYDROXY-BENZAMIDINE Preparation Products And Raw materials
Raw materials
Preparation Products
2-AMINO-N-HYDROXY-BENZAMIDINE Suppliers
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- India
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