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Home > Encyclopedia > Benzamidine, hydrochloride

Benzamidine, hydrochloride

Benzamidine, hydrochloride structure

Benzamidine, hydrochloride 

structure
  • CAS No:

    1670-14-0

  • Formula:

    C7H8N2.ClH

  • Chemical Name:

    Benzamidine, hydrochloride

  • Synonyms:

    Benzenecarboximidamide,hydrochloride (1:1);Benzamidine,monohydrochloride;Benzenecarboximidamide,monohydrochloride;Benzamidine,hydrochloride;Benzamidinium chloride;Amidinobenzene hydrochloride;Benzimidamide hydrochloride;Benzamidine hydrochloride;143504-23-8;2375087-53-7

  • Categories:

    Active Pharmaceutical Ingredients  >  Other Chemical Drugs

Description

white to off-white powder

Benzamidine, hydrochloride Basic Attributes

156.61

156.045425

216-795-4

0G112W4L27

2020

DTXSID9044401

29252900

Characteristics

49.9

2.57270

White to off-white Powder

1.09 g/cm3

86-88 °C

332.9ºC at 760 mmHg

155.1ºC

soluble

2-8°C

5.63E-05mmHg at 25°C

Peritoneal-mouse LD50: 580 mg/kg

Flammable; burning produces fumes of toxic nitrogen oxides, chlorides and hydrogen chloride

Safety Information

NONH for all modes of transport

3

36/37/38

26-37/39-36

CV6260000

Xi

Ventilated, low temperature and dry

Stable at room temperature in closed containers under normal storage and handling conditions.

P305 + P351 + P338

H315-H319

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 61 companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Toxicity

moderately toxic

Drug Information

Exogenous or endogenous compounds which inhibit SERINE ENDOPEPTIDASES. (See all compounds classified as Serine Proteinase Inhibitors.)

benzamidine

Benzamidine, hydrochloride Use and Manufacturing

Methods of Manufacturing

Benzal oxime (272 g, 2.0 mol, 1.0 eq), methanol (500 mL) and Raney Ni (15 g) were charged into a 1 L autoclave. A small amount of liquid ammonia was charged and N2 was substituted three times. H2 was then added to maintain the autoclave Pressure 2-3MPa, temperature control 50 , the reaction until no longer hydrogen absorption, after the end of the reaction, filtration, the filtrate was concentrated to dryness, the residue was cooled to 5 , the solid precipitation, filtration, to get gray crude benzamidine hydrochloride , Then add ethanol (700mL) heated completely dissolved, then add activated carbon bleaching, refluxing 30min, filtered while hot, cooled to 0 ° C, filtered and dried at 50 ° C in vacuo to give a white solidBenzamidine hydrochloride 325 g, yield 94.1percent, HPLC purity 99.6percent.The first step was to synthesize intermediate 1. To a 250mL three-necked flask were added cyanobenzene (0.5 mol)and C

Uses

For biochemical research

Benzenecarboximidamide, hydrochloride (1:1): ACTIVE

Computed Properties

Molecular Weight:156.61
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:156.0454260
Monoisotopic Mass:156.0454260
Topological Polar Surface Area:49.9
Heavy Atom Count:10
Complexity:104
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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