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Fenspiride hydrochloride

CAS No.
5053-08-7
Chemical Name:
Fenspiride hydrochloride
Synonyms
jp428;Erespal;NAT 333;espiran;fluiden;Tegencia;Decaspir;pneumorel;Viarespan;NDR 5998A
CBNumber:
CB7295887
Molecular Formula:
C15H21ClN2O2
Molecular Weight:
296.8
MDL Number:
MFCD00133315
MOL File:
5053-08-7.mol
Last updated:2024-11-19 20:33:22

Fenspiride hydrochloride Properties

Melting point 235-238°C (dec.)
storage temp. Refrigerator
solubility DMSO (Slightly), Methanol (Slightly), Water (Slightly)
form powder
color white
FDA UNII 832NBX878V

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H332-H312
Precautionary statements  P264-P270-P301+P312-P330-P501-P261-P271-P304+P340-P312-P280-P302+P352-P312-P322-P363-P501
Hazard Codes  Xn
Risk Statements  20/21/22
Safety Statements  36
WGK Germany  3
RTECS  RO0375000
HS Code  2934.99.3000
Toxicity LD50 i.v. in mice: 106 mg/kg; orally in rats: 437 mg/kg (LeDouarec)
NFPA 704
0
3 0

Fenspiride hydrochloride price More Price(16)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical F1211 Fenspiride Hydrochloride 5053-08-7 1G $61 2024-03-01 Buy
TCI Chemical F1211 Fenspiride Hydrochloride 5053-08-7 5G $171 2024-03-01 Buy
Cayman Chemical 25512 Fenspiride (hydrochloride) ≥95% 5053-08-7 5g $56 2024-03-01 Buy
Cayman Chemical 25512 Fenspiride (hydrochloride) ≥95% 5053-08-7 10g $97 2024-03-01 Buy
Cayman Chemical 25512 Fenspiride (hydrochloride) ≥95% 5053-08-7 25g $216 2024-03-01 Buy
Product number Packaging Price Buy
F1211 1G $61 Buy
F1211 5G $171 Buy
25512 5g $56 Buy
25512 10g $97 Buy
25512 25g $216 Buy

Fenspiride hydrochloride Chemical Properties,Uses,Production

Pharmacological effects

As an α adrenergic and H1 histamine receptor antagonist, Fenspiride has been shown to be antiinflammatory, anti-allergic and antioxidant. Fenspiride inhibited SO2-induced goblet cell hyperplasia in rats, with concomitant inhibition of increased hexose and fucose, indicative of mucus hypersecretion, in lavage fluid. Fenspiride also exhibits neuronal inhibitory activity. For example, in guinea pigs, it reverses capsaicin-induced and citric acid-induced bronchoconstriction and cough, and inhibits cholinergic and non-adrenergic, non-cholinergic (NANC) neural contraction of isolated bronchi.

Indications

Fenspiride hydrochloride is a bronchodilator, which was used as a drug in the treatment of certain respiratory diseases. Finsecbili hydrochloride against serotonin, dilating bronchial smooth muscle, the intensity of action is between isoproterenol and theophylline, in addition to reducing the resistance of air movement in the lungs, experiments have shown that this product has dilated bronchial smooth muscle, antitussive, antipyretic and analgesic effects. Suitable for chronic bronchitis, bronchial asthma and chronic respiratory insufficiency.  In Russia it was approved for the treatment of acute and chronic inflammatory diseases of ENT organs and the respiratory tract, as well as for maintenance treatment of asthma (like rhinopharyngitis, laryngitis, tracheobronchitis, otitis and sinusitis).

Chemical Properties

Pale Yellow Solid

Originator

Viarespan,Servier,France,1969

Uses

Antiinflammatory;Bradykinin antagonist

Uses

Bronchodilator with anti-inflammatory properties. Inhibits mucus secretion and reduces the release of tachykinins at a prejunctional level by its anti-muscarinic action. It also may be an antagonist at α adrenergic and H1 histamine receptors.

Manufacturing Process

A solution of 192 g of 1-phenethyl-4-hydroxy-4-aminomethyl piperidine in 800 cc of diethylcarbonate is heated for 2? hours to reflux at about 80°C in the presence of sodium methylate (prepared for immediate use from 2 g of sodium). After this time, the ethyl alcohol formed during the reaction is slowly distilled while the maximum temperature is reached. The excess ethyl carbonate is distilled under reduced pressure. A crystallized residue is then obtained, which is stirred with 400 cc of water and 400 cc of ether. The solution is filtered and 125 g (77.6%) of practically pure product melting at 232°C to 233°C, are obtained.
The starting material was prepared in a yield of 58% by reduction of the corresponding cyanohydrin. It in turn was prepared from 1-(2-phenylethyl)-4- piperidone and potassium cyanide to give the cyanohydrin which was reduced by lithium aluminum hydride.

Therapeutic Function

Bronchodilator

Fenspiride hydrochloride Preparation Products And Raw materials

Global( 143)Suppliers
Supplier Tel Email Country ProdList Advantage
Nanjing Gold Pharmaceutical Technology Co. Ltd.
025-84209270 15906146951 CHINA 115 55
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21634 55
Hangzhou FandaChem Co.,Ltd.
+8615858145714 FandaChem@Gmail.com China 9214 55
Shanghai Yingrui Biopharma Co., Ltd.
+86-21-33585366 - 03@ sales03@shyrchem.com CHINA 738 60
Jinan Chenghui-Shuangda Chemical Co.,Ltd
+86-531-58897082 ericqiao@jnchsd.com CHINA 158 58
Jinan Shengqi pharmaceutical Co,Ltd
86+18663751872 christine@shengqipharm.com CHINA 491 58
Xiamen AmoyChem Co., Ltd
+86-86-5926051114 +8618959220845 sales@amoychem.com China 6383 58
HubeiwidelychemicaltechnologyCo.,Ltd
18627774460 faith@widelychemical.com CHINA 742 58
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22963 58
Shanghai Longyu Biotechnology Co., Ltd.
+8619521488211 info@longyupharma.com China 2529 58

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View Lastest Price from Fenspiride hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Fenspiride hydrochloride pictures 2024-11-19 Fenspiride hydrochloride
5053-08-7
US $30.00-95.00 / mg 99.78% 10g TargetMol Chemicals Inc.
Fenspiride hydrochloride pictures 2024-11-19 Fenspiride hydrochloride
5053-08-7
US $30.00-95.00 / mg 99.78% 10g TargetMol Chemicals Inc.
Fenspiride hydrochloride pictures 2021-08-18 Fenspiride hydrochloride
5053-08-7
US $1.00 / g 1g 99% 10tons Hebei Binshare New Material Co. Ltd

Fenspiride hydrochloride Spectrum

1-Oxa-3,8-diazaspiro[4.5]decan-2-one, 8-(2-phenylethyl)-, hydrochloride (1:1) 2-OXAZOLIDINONE-5-SPIRO-4'-[N-(2-PHENYLETHYL)PIPERIDINE] HYDROCHLORIDE FENSPIRIDE HYDROCHLORIDE 8-(2-phenylethyl)-1-oxa-3,8-diazaspiro(4.5)decan-2-onehydrochloride 8-diazaspiro(4.5)decan-2-one,8-(2-phenylethyl)-1-oxa-monohydrochloride 8-diazaspiro(4.5)decan-2-one,8-phenethyl-1-oxa-monohydrochloride 8-n-fenetil-1-oxa-2-oxo-3,8-diazaspiro-(4,5)-decanocloridrato pneumorel tegenciahydrochloride 1-Oxa-3,8-diazaspiro(4.5)decan-2-one, 8-(2-phenylethyl)-, monohydrochl oride Tegencia Viarespan 8-phenethyl-1-oxa-3,8-diazaspiro[4.5]decan-2-one hydrochloride Fenspiride HCl Decaspir Erespal NAT 333 NDR 5998A Fenspiride hydrochloride, >=99% oxa-monohydrochloride Fensipiride HCL chlorhydratedephenethyl-8-oxa-1-diaza-3,8-spiro(4,5)decanone-2 decaspiride espiran fluiden jp428 nat-333hydrochloride ndr-5998ahydrochloride phenethyl-8-oxa-1-diaza-3,8-spiro(4,5)decanone-2-hydrochloride Fenspiride HydrochlorideQ: What is Fenspiride Hydrochloride Q: What is the CAS Number of Fenspiride Hydrochloride Q: What is the storage condition of Fenspiride Hydrochloride Q: What are the applications of Fenspiride Hydrochloride ‘5053-08-7 Hot selling Fenspiride CAS:5053-08-7 in stock Tiamulin fumarate CAS 55297-96-6 Fenspiride hydrochloride CAS NO.5053-08-7 High quality hot sale CAS:5053-08-7 Fenspiride Hcl CAS NO.5053-08-7 Hot Selling Fenspiride hydrochloride Fenspiride hcl CAS NO.5053-08-7 Fencipril hydrochloride 5053-08-7 Immune Cell Signaling and Blood Immune System Regulation Immunomodulators and Antibiotics Cell Signaling and Neuroscience Cell Biology BioChemical Amines Aromatics Heterocycles Intermediates & Fine Chemicals Pharmaceuticals