857661
4-Aminobenzamidine dihydrochloride
98%
Synonym(s):
p-Aminobenzimidamide dihydrochloride
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About This Item
Linear Formula:
H2NC6H4C(=NH)NH2·2HCl
CAS Number:
Molecular Weight:
208.09
Beilstein:
3692927
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
form
crystals
mp
>300 °C (lit.)
functional group
amine
storage temp.
2-8°C
SMILES string
Cl[H].Cl[H].NC(=N)c1ccc(N)cc1
InChI
1S/C7H9N3.2ClH/c8-6-3-1-5(2-4-6)7(9)10;;/h1-4H,8H2,(H3,9,10);2*1H
InChI key
GHEHNICLPWTXJC-UHFFFAOYSA-N
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Application
4-Aminobenzamidine dihydrochloride can be used to synthesize:
- Orally active fibrinogen receptor antagonists based on benzamidines.[1]
- Benzamidine derivatives that are selective and potent serine protease inhibitors.[2][3]
- Novel pyrrolo [3,2-c] quinolines that are structural analogs of topoisomerase inhibitors such as coralyne and fagaronine.[4]
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Biochemical and molecular modeling analysis of the ability of two p-aminobenzamidine-based sorbents to selectively purify serine proteases (fibrinogenases) from snake venoms.
De-Simone S G, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 822(1-2), 1-9 (2005)
In vitro blood compatibility of polymeric biomaterials through covalent immobilization of an amidine derivative.
Gouzy M F, et al.
Biomaterials, 25(17), 3493-3501 (2004)
Design of orally active, non-peptide fibrinogen receptor antagonists. An evolutionary process from the RGD sequence to novel anti-platelet aggregation agents.
Bovy P R, et al.
Bioorganic & Medicinal Chemistry, 2(9), 881-895 (1994)
Specific adsorption of serine proteases on coated silica beads substituted with amidine derivatives.
S Khamlichi et al.
Journal of chromatography, 510, 123-132 (1990-06-27)
Amidine derivatives interact with serine proteases, the inhibition being due to interactions between amidine functions and the active sites of the enzymes. Five different types of amidine (substituted or unsubstituted) were coupled to coated silica beads, which had previously been
A synthesis of new pyrrolo [3, 2?c] quinolines.
Dudouit F, et al.
Journal of Heterocyclic Chemistry, 38(3), 755-758 (2001)
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