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Romifidine hydrochloride

Romifidine hydrochloride Structure
CAS No.
65896-14-2
Chemical Name:
Romifidine hydrochloride
Synonyms
Sedivet;STH 2130Cl;Romifidine HCl;Romifidine Hydrochloride;Romifidine Hydrochloride, Monohydrochloride;N-(2-Bromo-6-fluorophenyl)-4,5-dihydro-1H-imidazol-2-ylamine HCl;N-(2-BroMo-6-fluorophenyl)-4,5-dihydro-1H-iMidazol-2-aMine Hydrochloride;1H-Imidazol-2-amine, N-(2-bromo-6-fluorophenyl)-4,5-dihydro-, monohydrochloride;1H-Imidazol-2-amine, N-(2-bromo-6-fluorophenyl)-4,5-dihydro-, hydrochloride (1:1)
CBNumber:
CB51210096
Molecular Formula:
C9H10BrClFN3
Molecular Weight:
0
MOL File:
65896-14-2.mol
Modify Date:
2024/7/14 20:44:35

Romifidine hydrochloride Properties

storage temp. Inert atmosphere,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly), Water (Slightly)
form Solid
color White
InChI InChI=1S/C9H9BrFN3.ClH/c10-6-2-1-3-7(11)8(6)14-9-12-4-5-13-9;/h1-3H,4-5H2,(H2,12,13,14);1H
InChIKey SDXVSIWCVTYYQN-UHFFFAOYSA-N
SMILES C1(NC2=C(F)C=CC=C2Br)NCCN=1.[H]Cl

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Romifidine hydrochloride Chemical Properties,Uses,Production

Description

Romifidine hydrochloride [N-(2-b romifidineo-6-fluoro-phenyl)- 4,5-dihydro-1H-imidazol-2-amine mono-hydrochloride, C9H9BrFN3, MW 258.1; romifidine] is an imidazole derivative with potent a2-adrenoceptor agonist properties. It is commonly used in equine practice to provide sedation, analgesia, and muscle relaxation. A comparative study reported that an intravenous (i.v.) dose of 80 μg/kg romifidine is equipotent to 1 mg/kg xylazine i.v. and 20 μg/kg detomidine i.v.[1]. Typical signs of sedation include muscle relaxation, decreased head height (HH), diminished responsiveness to external stimuli, and postural abnormalities following romifidine administration. Furthermore, romifidine possesses antinociceptive activity. As an analgesic, it reduces anesthetic requirements for isoflurane in horses.

Uses

An α2 agonist use as a sedative and analgesic.

Mechanism of action

Alpha2 agonists decrease release of neurotransmitters from the neuron. The proposed mechanism whereby they decrease transmission is via binding to presynaptic alpha2 receptors (negative feedback receptors).

References

[1] M. WOJTASIAK-WYPART. “Pharmacokinetic profile and pharmacodynamic effects of romifidine hydrochloride in the horse.” Journal of veterinary pharmacology and therapeutics 35 5 (2012): 478–488.

Romifidine hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 36)Suppliers
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CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6257 58 Inquiry
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Tianjin Kilo Pharmaceutical Sci-Tech Co., Ltd +86-02223869539 +86-15560057295 China 27 58 Inquiry
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Shaanxi Dideu Medichem Co. Ltd +86-29-81148696 +86-15536356810 China 3882 58 Inquiry
BOC Sciences +1-631-485-4226 United States 19553 58 Inquiry
AFINE CHEMICALS LIMITED +86-0571-85134551 China 15361 58 Inquiry
Nanjing Doge Biomedical Technology Co., Ltd +86-25-58227606 +86-15305155328 China 4128 58 Inquiry
Zibo Hangyu Biotechnology Development Co., Ltd +86-0533-2185556 +8617865335152 China 10986 58 Inquiry
LEAPCHEM CO., LTD. +86-852-30606658 China 43340 58 Inquiry

65896-14-2(Romifidine hydrochloride)Related Search:

1H-Imidazol-2-amine, N-(2-bromo-6-fluorophenyl)-4,5-dihydro-, monohydrochloride Romifidine Hydrochloride N-(2-BroMo-6-fluorophenyl)-4,5-dihydro-1H-iMidazol-2-aMine Hydrochloride Sedivet STH 2130Cl Romifidine Hydrochloride, Monohydrochloride Romifidine HCl 1H-Imidazol-2-amine, N-(2-bromo-6-fluorophenyl)-4,5-dihydro-, hydrochloride (1:1) N-(2-Bromo-6-fluorophenyl)-4,5-dihydro-1H-imidazol-2-ylamine HCl 65896-14-2 C9H10BrClFN3 Amines Aromatics Heterocycles Intermediates & Fine Chemicals Pharmaceuticals