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Thermo Scientific Chemicals
Benzamidine hydrochloride hydrate, 98%, water ca 10-14%
CAS: 206752-36-5 | C7H9ClN2 | 156.61 g/mol
化学物質識別子
CAS206752-36-5
IUPAC Namebenzenecarboximidamide hydrochloride
Molecular FormulaC7H9ClN2
InChI KeyLZCZIHQBSCVGRD-UHFFFAOYSA-N
SMILESCl.NC(=N)C1=CC=CC=C1
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)White
FormPowder
Assay (Titration ex Chloride)> 97.5 to <102.5% (Dry wt. basis)
Water Content (Karl Fischer Titration)<18.0%
Benzamidine hydrochloride hydrate is a reversible inhibitor of trypsin, trypsin-like enzymes, and serine proteases. It is a proteolytic inhibitor and apoptosis reagent.
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
Benzamidine hydrochloride hydrate is a reversible inhibitor of trypsin, trypsin-like enzymes, and serine proteases. It is a proteolytic inhibitor and apoptosis reagent.
Solubility
Soluble in water.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents. It is hygroscopic in nature.
Benzamidine hydrochloride hydrate is a reversible inhibitor of trypsin, trypsin-like enzymes, and serine proteases. It is a proteolytic inhibitor and apoptosis reagent.
Solubility
Soluble in water.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents. It is hygroscopic in nature.
RUO – Research Use Only
General References:
- A Bini, J J Fenoglio Jr, R Mesa-Tejada, B Kudryk, K L Kaplan. Identification and distribution of fibrinogen, fibrin, and fibrin(ogen) degradation products in atherosclerosis. Use of monoclonal antibodies. Arteriosclerosis, Thrombosis, and Vascular Biology. 1989, 9 109-121.
- Frederick G. Bordwell, Guo Zhen Ji. Effects of structural changes on acidities and homolytic bond dissociation energies of the hydrogen-nitrogen bonds in amidines, carboxamides, and thiocarboxamides. J. Am. Chem. Soc. 1991, 113 (22), 8398-8401.