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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
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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
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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.

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N-Bromosuccinimide Price

Cayman Chemical
Product number
11062
Product name
2-amino Benzamidoxime
Purity
≥97%
Packaging
1g
Price
$66
Updated
2024/03/01
Cayman Chemical
Product number
11062
Product name
2-amino Benzamidoxime
Purity
≥97%
Packaging
5g
Price
$274
Updated
2024/03/01
Cayman Chemical
Product number
11062
Product name
2-amino Benzamidoxime
Purity
≥97%
Packaging
500mg
Price
$36
Updated
2024/03/01
TRC
Product number
A577125
Product name
2-AminobenzamideOxime
Packaging
10mg
Price
$45
Updated
2021/12/16
TRC
Product number
A577125
Product name
2-AminobenzamideOxime
Packaging
50mg
Price
$55
Updated
2021/12/16
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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

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2-AMINO-N-HYDROXY-BENZAMIDINE Suppliers

Shanghai Boyle Chemical Co., Ltd.
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021-50182298 021-50180596
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+86-21-57758967
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sales@boylechem.com
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China
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J & K SCIENTIFIC LTD.
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18210857532; 18210857532
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86-10-82849933
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jkinfo@jkchemical.com
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China
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Alfa Aesar
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400-6106006
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021-67582001/03/05
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saleschina@alfa-asia.com
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China
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Wuhan Chemwish Technology Co., Ltd
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86-027-67849912
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Shanghai Sinch Parmaceuticals Tech. Co. Ltd.
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+86-21-54098501
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sales@sinch.com.cn
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Shandong Xiya Chemical Co., Ltd
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13355009207 13355009207
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Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.
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025-66028182 17714375163
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SanoChem (Chengdu) Tech. Co., Ltd.
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China
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Wuhan Chemwish Technology Co., Ltd
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027-67849912
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027-87531808
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sales@chemwish.com
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China
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Shanghai YuanYe Biotechnology Co., Ltd.
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021-61312847; 18021002903
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