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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
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 02:36:10

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)  Exclamation Mark (GHS07)
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(35)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical F1211 Fenspiride Hydrochloride 5053-08-7 1G $47 2026-04-30 Buy
TCI Chemical F1211 Fenspiride Hydrochloride 5053-08-7 5G $130 2026-04-30 Buy
Cayman Chemical 25512 Fenspiride (hydrochloride) ≥95% 5053-08-7 5g $62 2026-04-30 Buy
Cayman Chemical 25512 Fenspiride (hydrochloride) ≥95% 5053-08-7 10g $107 2026-04-30 Buy
Cayman Chemical 25512 Fenspiride (hydrochloride) ≥95% 5053-08-7 25g $238 2026-04-30 Buy
Product number Packaging Price Buy
F1211 1G $47 Buy
F1211 5G $130 Buy
25512 5g $62 Buy
25512 10g $107 Buy
25512 25g $238 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 Suppliers ( 154)
Supplier Tel Email Country ProdList Advantage
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32273 50
Tianjin heowns Biochemical Technology Co., Ltd. 400 638 7771 sales@heowns.com China 14412 57
Dalian Meilun Biotech Co., Ltd. 0411-62910999 13889544652 sales@meilune.com China 4765 58
Tianjin Branch Chong pharmaceutical intermediates Co., Ltd. 022-60116533 13207668525 saleskc@scipharmacn.com China 360 58
Haoyuan Chemexpress Co., Ltd. 021-58950125 info@chemexpress.com China 7545 61
TOKYO CHEMICAL INDUSTRY CO., LTD. 03-36680489 Sales-JP@TCIchemicals.com Japan 28364 80
TCI Europe 320-37350700 sales@tcieurope.eu Europe 23654 75
TCI AMERICA 800-4238616 sales@tciamerica.com Americas 23636 75
MedChemexpress LLC 021-58955995 sales@medchemexpress.cn United States 4853 58

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View Latest Price from Fenspiride hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Fenspiride hydrochloride pictures 2026-08-08 Fenspiride hydrochloride
5053-08-7
$29.00 99.64% 10g TargetMol Chemicals Inc.
Fenspiride hydrochloride pictures 2026-08-08 Fenspiride hydrochloride
5053-08-7
$29.00 99.64% 10g TargetMol Chemicals Inc.
Fenspiride Hydrochloride pictures 2026-08-07 Fenspiride Hydrochloride
$1.00 1KG 99% 50 tons Shaanxi Dideu Medichem 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 Fencipril hydrochloride Hot Selling Fenspiride hydrochloride Fenspiride hcl CAS NO.5053-08-7 High quality hot sale CAS:5053-08-7 Fenspiride Hcl CAS NO.5053-08-7 Fenspiride hydrochloride CAS NO.5053-08-7 Hot selling Fenspiride CAS:5053-08-7 in stock 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 ‘5053-08-7 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 Fenspiride hydrochloride, 10 mM in DMSO 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