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Home > Encyclopedia > Robenidine hydrochloride

Robenidine hydrochloride

Robenidine hydrochloride structure

Robenidine hydrochloride 

structure
  • CAS No:

    25875-50-7

  • Formula:

    C15H13Cl2N5.ClH

  • Chemical Name:

    Robenidine hydrochloride

  • Synonyms:

    Carbonimidic dihydrazide,2,2′-bis[(4-chlorophenyl)methylene]-,hydrochloride (1:1);Guanidine,1,3-bis[(p-chlorobenzylidene)amino]-,monohydrochloride;Carbonimidic dihydrazide,bis[(4-chlorophenyl)methylene]-,monohydrochloride;Robenzidene;Robenidine hydrochloride;1,3-Bis[(p-chlorobenzylidene)amino]guanidine monohydrochloride;Cycostat;NCL 812;2,2′-Bis[(4-chlorophenyl)methylene]carbonimidic dihydrazide hydrochloride;12692-91-0

  • Categories:

    Active Pharmaceutical Ingredients  >  Antiparasitic Drugs

Description

Off-White Solid


An anticoccidial agent mainly for poultry.

Robenidine hydrochloride Basic Attributes

370.66

369.031

247-307-8

8STT15Y392

Characteristics

75.1

5.15890

Off-White Solid

289-290 °C

488.1ºC at 760 mmHg

249ºC

0-6°C

1.12E-09mmHg at 25°C

Safety Information

2

22

ME8651000

Xn

P264, P270, P273, P301+P312, P330, P391, P501

H302

|Warning|H302 (95.35%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P301+P312, P330, and P501|Aggregated GHS information provided by 43 companies from 5 notifications to the ECHA C&L Inventory.

Drug Information

Agents useful in the treatment or prevention of COCCIDIOSIS in man or animals. (See all compounds classified as Coccidiostats.)

Cytostat

Robenidine hydrochloride Use and Manufacturing

Methods of Manufacturing

It is obtained from sulfamididine as raw material and cyclized with acetylacetone. Sulfamidam, acetylacetone, sodium bisulfite, sodium hydroxide and water were put into the reaction kettle and heated to reflux for about 6h. When crystallization occurs in the reaction solution, continue to reflux for 20 hours after adding acetylacetone. After recovering acetylacetone, add appropriate amount of boiling water and filter while hot. The filter cake is washed with hot water, recrystallized and dried to obtain sulfamethazine.

Uses

Robenidine is used as a coccidiostat.

Animal Drugs -> FDA Approved Animal Drug Products (Green Book) -> Active Ingredients

Computed Properties

Molecular Weight:370.7
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:369.031479
Monoisotopic Mass:369.031479
Topological Polar Surface Area:75.1
Heavy Atom Count:23
Complexity:408
Defined Bond Stereocenter Count:3
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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