Basic information
- CAS
1670-14-0- Standard SMILES
Cl.N=C(N)c1ccccc1- InChIKey
LZCZIHQBSCVGRD-UHFFFAOYSA-N- Molecular formula
- C7H8N2.ClH
- Average molar mass
- 156.61 g/mol
- Monoisotopic mass
- 156.04542597
Names & identifiers
- Preferred name
- Benzamidine, hydrochloride
- IUPAC
- benzenecarboximidamide;hydrochloride
- English name
- Benzamidine hydrochloride
- Molecular formula
- C7H9ClN2
- Molecular weight
- 156.61
Names & synonyms
Show more names
Database identifiers
- CAS
1670-14-0- PubChem CID
- 80289
- DTXSID
DTXSID9044401- ChEMBL
CHEMBL537204- UNII
- 0G112W4L27
- EC Number
- 216-795-4
Properties
Computed structural properties
- Topological polar surface area
- 49.9 Ų
- Hydrogen bond donors
- 3
- Hydrogen bond acceptors
- 1
- Rotatable bonds
- 1
- Heavy atoms
- 10
- Formal charge
- 0
- Complexity
- 103
Experimental & physicochemical properties
Physicochemical properties
- Melting point
- 86 · 86-88 °C(lit.)
- storage temp.
- 2 · 2-8°C
- solubility
- 25 mg/mlDMSO: · DMF: 25 mg/mlDMSO: 25 mg/mlEthanol: 10 mg/mlPBS (pH 7.2): 3 mg/ml
- form
- Powder
- color
- White to off-white
- PH
- 4 to · 4.0 to 6.5(50g/L, 25 ℃)
- Water Solubility
- soluble
- BRN
- 3594959 · 3594959
- Stability
- 2 years · Stable for 2 years from date of purchase as supplied. Solutions are not stable and must be prepared fresh daily
- InChI
- InChI=1S/C7H8N2.ClH/c8-7(9)6-4-2-1-3-5-6;/h1-5H,(H3,8,9);1H
- InChIKey
- LZCZIHQBSCVGRD-UHFFFAOYSA-N
- SMILES
- C1(C(=N)N)=CC=CC=C1.Cl
- CAS DataBase Reference
- 1670 · 1670-14-0(CAS DataBase Reference)
- FDA UNII
- 0 G112W4L27 · 0G112W4L27
- EPA Substance Registry System
- Benzenecarboximidamide, monohydrochloride (1670-14-0)
- UNSPSC Code
- 12352202 · 12352202
- NACRES
- 77 · NA.77
- Symbol(GHS)
- 7 · GHS07
- Signal word
- Warning
- Hazard statements
- 315 · H315-H319
- Precautionary statements
- 264 · P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
- Hazard Codes
- Xi
- Risk Statements
- 36 · 36/37/38
- Safety Statements
- 26 · 26-37/39-36
- WGK Germany
- 3 · 3
- RTECS
- 6260000 · CV6260000
- F
- 3 · 3-21
- TSCA
- TSCA listed
- HS Code
- 29252900 · 29252900
- Storage Class
- 11 · 11 - Combustible Solids
- REACH Registrations
- Active
Safety & regulation
GHS classification
GHS Classification
Warning
H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 166 reports by companies from 12 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard information
Regulatory Information
Chemical: Benzenecarboximidamide, monohydrochloride
Status: Active Update: 24-06-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/24030
Benzenecarboximidamide, monohydrochloride: Does not have an individual approval but may be used under an appropriate group standard
Safety data
- F
- 3-21
- wgk
- 3
- tsca
- TSCA listed
- rtecs
- CV6260000
- hs_code
- 29252900
- risk_code
- 36/37/38
- Signal word
- Warning
- Symbol(GHS)
- GHS07
- hazard_code
- Xi
- safety_code
- 26-37/39-36
- Storage Class
- 11 - Combustible Solids
- Hazard statements
- H315-H319
- REACH Registrations
- Active
- Precautionary statements
- P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Chemistry & industry
Pharmacology
Uses & manufacturing
Applications
DescriptionBenzamidine hydrochloride is a reversible inhibitor of trypsin, trypsin-like enzymes, and serine proteases. A concentration of approximately 1 mM is used for general protease inhibition. To inhibit proteases from yeast, a range of 0.5 to 4.0 mM is used and it is for the most part interchangeable with pepstatin A.In addition to being a strong competitive inhibitor of trypsin, benzamidine HCl has been also shown to be a strong competitive inhibitor of thrombin and plasmin. It was also found to be as effective as aprotinin in the prevention of glucagon degradation in human plasma.
UsesBenzamidine is a reversible inhibitor of serine proteases, including trypsin, plasmin, and thrombin (Kis = 35, 350, and 220 μM, respectively). In addition to its use as a general serine protease inhibitor, benzamidine is used, when immobilized, to purify novel proteases.
Preparation methods
PreparationTo a stainless steel rocking autoclave equipped with a stirrer is added 103.0 gm (1.0 mole) of benzonitrile, 214.0 gm (4.0 mole) of ammonium chloride, and 306.0 gm (18.0 mole) of ammonia is introduced by means of a transfer bomb. The reaction mixture is heated at 150°C for 18 hr (pressure: 1300-6500 psig), cooled, and, with appropriate precautions for the safe control of the excess ammonia, is vented to atmospheric pressure. The reaction mixture is extracted with ether to remove approximately 5% unreacted benzonitrile, and then extracted with hot acetonitrile or ethanol to separate the amidine hydrochloride from the unreacted ammonium chloride. Concentration of the latter affords 120.5 gm (77%) of benzamidine hydrochloride, m.p. 161-163°C.
Upstream & downstream products
Upstream raw materials
Downstream products
Suppliers101 total
Related reactions
Compound notes
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