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CYPROHEPTADINE HYDROCHLORIDE

CAS No.
969-33-5
Chemical Name:
CYPROHEPTADINE HYDROCHLORIDE
Synonyms
CYPROHEPTADINE HCL;4-(5H-DIBENZO[A,D]CYCLOHEPTEN-5-YLIDINE)-METHYLPIPERIDINE HYDROCHLORIDE;nuran;peritol;ANAREXOL;periactinsyrup;CYPROHEPTADINE HCL BP;periactinhydrochloride;periactinolhydrochloride;Cyproheptadinhydrochlorid
CBNumber:
CB2698687
Molecular Formula:
C21H22ClN
Molecular Weight:
323.86
MDL Number:
MFCD00012538
MOL File:
969-33-5.mol
Last updated:2024-03-13 16:52:01

CYPROHEPTADINE HYDROCHLORIDE Properties

Melting point 254-256.5 °C(Solv: ethanol (64-17-5); ethyl ether (60-29-7))
storage temp. Inert atmosphere,Room Temperature
solubility ethanol: soluble
form solid
color Crystals from EtOH/Et2O
Water Solubility Soluble in water (15mM)
Stability Hygroscopic
FDA UNII 0S9323MCT0

Pharmacokinetic data

Protein binding 96-99%
Excreted unchanged in urine <2%
Volume of distribution Large
Biological half-life 1-4 / Increased

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08
Signal word  Warning
Hazard statements  H302-H361-H315-H319-H335
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P-P264-P270-P301+P312-P330-P501-P201-P202-P281-P308+P313-P405-P501-P264-P280-P302+P352-P321-P332+P313-P362
Hazard Codes  Xn
Risk Statements  22-36/37/38
Safety Statements  26-36
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
RTECS  TM7050000
HazardClass  6.1(b)
PackingGroup  III
Toxicity LD50 orl-rat: 295 mg/kg DRUGAY 6,340,82

CYPROHEPTADINE HYDROCHLORIDE price More Price(26)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
AK Scientific J53419 CyproheptadineHCl 969-33-5 5g $47.2 2021-12-16 Buy
Biosynth Carbosynth FC61445 Cyproheptadine hydrochloride 969-33-5 100mg $50 2021-12-16 Buy
ApexBio Technology B3309 Cyproheptadine hydrochloride 969-33-5 10mM(in 1mL DMSO) $50 2021-12-16 Buy
ApexBio Technology B3309 Cyproheptadine hydrochloride 969-33-5 1unit $28 2021-12-16 Buy
AK Scientific M230 CyproheptadineHCl 969-33-5 1g $29 2021-12-16 Buy
Product number Packaging Price Buy
J53419 5g $47.2 Buy
FC61445 100mg $50 Buy
B3309 10mM(in 1mL DMSO) $50 Buy
B3309 1unit $28 Buy
M230 1g $29 Buy

CYPROHEPTADINE HYDROCHLORIDE Chemical Properties,Uses,Production

Originator

Periactin,Merck Sharp and Dohme,US,1961

Uses

Antipruritic;5-HT antagonist

Uses

Cyproheptadine hydrochloride is an antihistamine in which antiserotonin activity has been demonstrated both in vivo and in vitro. As yet, however, there is no evidence that this action contributes to clinical therapeutic effects. Anticholinergic and sedative effects are observed. Cyproheptadine may be more effective than other H1 blockers in the management of cold urticaria.

Definition

ChEBI: The hydrochloride salt of cyproheptadine. Note that the drug named cyproheptadine hydrochloride generally refers to cyproheptadine hydrochloride sesquihydrate.

Manufacturing Process

(A) Preparation of 1-Methyl-4-Piperidyl-Magnesium Chloride: Magnesium turnings (5.45 g, 0.22 g-atom) were placed in a 500 ml 3-necked flask provided with a condenser, Hershberg stirrer and dropping funnel and protected with a drying tube. An atmosphere of dry nitrogen was maintained in the apparatus throughout the reaction. The magnesium was covered with 20 ml of dry tetrahydrofuran. A crystal of iodine and 1.2 g of ethyl bromide were added and after the reaction had subsided (formation of ethylmagnesium bromide) a solution of 29.4 g (0.22 mol) of 4-chloro-1-methyl-piperidine in dry tetrahydrofuran (total volume, 103 ml) was added dropwise at such a rate that gentle reflux was maintained.
The solution of 4-chloro-1-methylpiperidine in tetrahydrofuran was dried over calcium hydride at ice-bath temperature prior to use. When the addition of the halide was complete the reaction mixture was refluxed with stirring for one hour. In some subsequent experiments this period of refluxing was omitted with no deleterious result.
The solution of 4-chloro-1-methylpiperidine in tetrahydrofuran was dried over calcium hydride at ice-bath temperature prior to use. When the addition of the halide was complete the reaction mixture was refluxed with stirring for one hour. In some subsequent experiments this period of refluxing was omitted with no deleterious result.
The solvent was evaporated from the combined benzene extracts to give 33.4 g of a clear light brown resin. Crystallization from an alcohol-water mixture gave 19.5 g of 1-methyl-4-(5-hydroxy-5-dibenzo[a,e]cycloheptatrienyl)- piperidine, MP 156° to 157°C. Two recrystallizations from alcohol-water mixtures followed by two recrystallizations from benzene-hexane mixtures gave analytically pure product, MP 166.7° to 167.7°C.
(C) Preparation of 1-Methyl-4-(5-Dibenzo[a,e]Cycloheptatrienylidene)- Piperidine Hydrochloride: 1-Methyl-4-(5-hydroxy-5-dibenzo[a,e] cycloheptatrienyl)-piperidine (3.05 g, 0.01 mol) was dissolved in glacial acetic acid, 15 ml. The solution was saturated with dry hydrogen chloride with external cooling. A white solid separated. Acetic anhydride (3.07 g, 0.03 mol) was added and the mixture heated on the steam bath for one hour. The solid dissolved in the first 5 minutes of the heating period.
The reaction mixture was poured into 25 ml of water and the mixture made strongly basic with 10N sodium hydroxide solution. The mixture was extracted 3 times with 50 ml portions of benzene, the combined extracts washed with water and concentrated to a volume of approximately 50 ml. The solution was saturated with dry hydrogen chloride and the white crystalline product collected and dried. The yield of product, MP 251.6° to 252.6°C (dec.) was 2.5 g. Recrystallization from a mixture of absolute alcohol and absolute ether gave a product, MP 252.6° to 253.6°C. A sample was analyzed after drying for 7 hours at 110°C over phosphorus pentoxide in vacuo.
(D) Preparation of 1-Methyl-4-(5-Dibenzo[a,e]Cycloheptatrienylidene)- Piperidine: The hydrochloride salt, 4.3 g, was suspended in 100 ml of warm water and the mixture made strongly alkaline by the addition of 15 ml of 5% sodium hydroxide. The mixture was extracted with four 50 ml portions of benzene and the extracts dried over sodium sulfate. Evaporation of the benzene on the steam-bath at reduced pressure left 3.7 g (97%) of the base,MP 110.3° to 111.3°C. Recrystallization from a mixture of alcohol and water gave product, MP 112.3° to 113.3°C.

brand name

Periactin (Merck).

Therapeutic Function

Antipruritic, Antihistaminic, Appetite stimulant

General Description

Cyproheptadinehydrochloride, 4-(5H-dibenzo-[a,d]-cyclohepten-5-ylidine)-1-methylpiperidine hydrochloride sesquihydrate(Periactin), is slightly soluble in water and sparingly solublein alcohol.
Cyproheptadine possesses both antihistamine and antiserotoninactivity and is used as an antipruritic agent. It isindicated for the treatment of hypersensitivity reactions,perennial, and seasonal allergic rhinitis; vasomotor rhinitis;allergic conjunctivitis, uncomplicated allergic skin manifestationsof urticaria and angioedema; amelioration of allergicreactions to blood or plasma; and cold urticaria. It is alsoused off-label for nightmares associated with posttraumaticstress disorder (PTSD), prevention of migraine, suppressionof vascular headaches, and appetite stimulation. Sedation isthe most prominent side effect, and this is usually brief, disappearingafter 3 or 4 days of treatment.

Biological Activity

Non-selective 5HT 2 antagonist, migraine prophylactic.

Safety Profile

Poison by ingestion and intraperitoneal routes. Human systemic effects by ingestion: jaundice, liver function tests impaired, gastrointestinal effects. An experimental teratogen. Experimental reproductive effects. Human mutation data reported. Whenheated

Drug interactions

Potentially hazardous interactions with other drugs
Analgesics: sedative properties increased with opioid analgesics.

Metabolism

Undergoes almost complete metabolism in the liver. The main metabolite found in humans is a quaternary ammonium glucuronide conjugate of cyproheptadine. 40% is excreted in the urine mainly as metabolites and 2-20% via the faeces.

storage

Room temperature

References

[1] levine b, green-johnson d, hogan s, smialek je. a cyproheptadine fatality. j anal toxicol. 1998 jan-feb;22(1):72-4.
[2] lin oa, karim za, vemana hp, espinosa ev, khasawneh ft. the antidepressant 5-ht2a receptor antagonists pizotifen and cyproheptadine inhibit serotonin-enhanced platelet function. plos one. 2014 jan 23;9(1):e87026.

3967-32-6
969-33-5
Synthesis of CYPROHEPTADINE HYDROCHLORIDE from 5-(1-Methyl-4-Piperidyl)5H-Dibenzo

CYPROHEPTADINE HYDROCHLORIDE Preparation Products And Raw materials

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View Lastest Price from CYPROHEPTADINE HYDROCHLORIDE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Cyproheptadine Hydrochloride pictures 2024-04-12 Cyproheptadine Hydrochloride
969-33-5
US $0.00 / kg 1kg 99% 2000ton Shaanxi Haibo Biotechnology Co., Ltd
CYPROHEPTADINE HYDROCHLORIDE pictures 2024-04-12 CYPROHEPTADINE HYDROCHLORIDE
969-33-5
US $3.00-1.00 / kg 1kg 99.9% 10 tons Shanghai Aosiris new Material Technology Co., LTD
CYPROHEPTADINE HYDROCHLORIDE pictures 2024-04-08 CYPROHEPTADINE HYDROCHLORIDE
969-33-5
US $100.00 / kg 1kg 99.9% 20tons Hong Kong Excellence Biotechnology Co., Ltd.
CYPROHEPTADINE HYDROCHLORIDE(GRP B SL NO.1124) 1-methyl-4-(5-dibenzo(a,e)cycloheptatrienylidene)piperidinehydrochloride 4-(5-dibenzo(a,e)cycloheptatrienylidene)piperidinehydrochloride 4-(5h-dibenzo(a,d)cyclohepten-5-ylidene)-1-methyl-piperidinhydrochloride cyproheptadienehydrochloride nuran CyproheptadineHclCyproheptadineHclBp CYPROHEPTADINEHYDROCHLORIDE(ANHYDROUS) ANAREXOL CYPROHEPTADINE HCL BP Cyproheptadine hydrochloride (Periactin) Cyproheptadine hydrochloride periactinhydrochloride periactinolhydrochloride periactinsyrup peritol Cycloheptadine Hydrochloride Cyproheptadine hydrochloride,CYPROHEPTADINE HCL, periactinolhydrochloride 4-(5H-dibenzo[a,d][7]annulen-5-ylidene)-1-methylpiperidine hydrochloride Cyproheptadine hydrochloride USP/EP/BP Cyproheptadine hydrochloride USP/EP/BP USP/EP/BP 1-Methyl-4-(5H-dibenzo[a,d]cyclohepten-5-ylidene)-piperidine hydrochloride CYPROHEPTADINE HCL 4-(5H-DIBENZO[A,D]CYCLOHEPTEN-5-YLIDINE)-METHYLPIPERIDINE HYDROCHLORIDE Cyproheptadinhydrochlorid Cyheptadine hydrochloride 969-33-5 354-29-4 C21H21NHCl1H2O C21H21NClH Building Blocks Heterocyclic Building Blocks Piperidines Serotonin receptor Active Pharmaceutical Ingredients