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Miconazole

CAS No.
22916-47-8
Chemical Name:
Miconazole
Synonyms
MICONAZOLE BASE;1H-Imidazole, 1-[2-(2,4-dichlorophenyl)-2-[(2,4-dichlorophenyl)methoxy]ethyl]- (9CI);r18134;mjr1762;R 18134;Minostate;Miconazol;NSC 170986;MICONAZOLE;Miconozole
CBNumber:
CB6493824
Molecular Formula:
C18H14Cl4N2O
Molecular Weight:
416.13
MDL Number:
MFCD00216019
MOL File:
22916-47-8.mol
MSDS File:
SDS
Last updated:2024-03-16 11:42:32

Miconazole Properties

Melting point 159-163C
Boiling point 555.1±50.0 °C(Predicted)
Density 1.5326 (rough estimate)
refractive index 1.6200 (estimate)
RTECS NI4770000
Flash point 87°(189°F)
storage temp. Sealed in dry,Room Temperature
solubility Very slightly soluble in water, freely soluble in methanol, soluble in ethanol (96 per cent).
pka pKa 6.91(H2O,t =25) (Uncertain)
color White to Off-White
Water Solubility Freely soluble in alcohols or acetone. Also soluble in DMF or chloroform. Insoluble in water
Sensitive Light Sensitive
CAS DataBase Reference 22916-47-8(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 7NNO0D7S5M
ATC code A01AB09,A07AC01,D01AC02,D01AC52,G01AF04,J02AB01,S02AA13
NIST Chemistry Reference Miconazole(22916-47-8)
EPA Substance Registry System 1H-Imidazole, 1-[2-(2,4-dichlorophenyl)-2-[(2,4-dichlorophenyl)methoxy]ethyl]- (22916-47-8)

Pharmacokinetic data

Protein binding 90%
Excreted unchanged in urine 1%
Volume of distribution 20(L/kg)
Biological half-life 24 / Unchanged

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H413
Precautionary statements  P264-P270-P273-P301+P312-P501
Hazard Codes  Xn
Risk Statements  22
Safety Statements  22-36
RIDADR  3249
WGK Germany  3
HazardClass  6.1(b)
PackingGroup  III
HS Code  2933290000

Miconazole price More Price(33)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHR1618 Miconazole 22916-47-8 1g $121 2024-03-01 Buy
Sigma-Aldrich 1443409 Miconazole 22916-47-8 200mg $436 2024-03-01 Buy
Alfa Aesar J60872 Miconazole, 99% 22916-47-8 1g $18.65 2024-03-01 Buy
Alfa Aesar J60872 Miconazole, 99% 22916-47-8 5g $47.65 2024-03-01 Buy
Sigma-Aldrich M1880000 Miconazole European Pharmacopoeia (EP) Reference Standard 22916-47-8 m1880000 $153 2024-03-01 Buy
Product number Packaging Price Buy
PHR1618 1g $121 Buy
1443409 200mg $436 Buy
J60872 1g $18.65 Buy
J60872 5g $47.65 Buy
M1880000 m1880000 $153 Buy

Miconazole Chemical Properties,Uses,Production

Chemical Properties

White or almost white powder.

Originator

Daktarin,Janssen,Italy,1974

Uses

Miconazole, is used as an antifungal inhibitor of aromatase. Miconazole has been shown to promote remyelination of neurons in chronic progressive multiple sclerosis mouse models. Miconazole is mainly used externally for the treatment of athlete's foot, ringworm, and jock itch. Internal application is used for oral or vaginal thrush (yeast infection). The oral gel may also be used for the lip disorder angular cheilitis. It is also used in photography.

Uses

Miconazole is an antifungal agent of the imidazole type. It is used in topical and vaginal preparations to prevent growth of dermatophytes, yeast, and molds.

Uses

Antifungal;Sterol 14-demethylase inhibitor.
Miconazole (Monistat-Derm, Micatin, etc.) is a synthetic imidazole antifungal compound that acts by altering cell membrane permeability. It is effective against most dermatophyte species, P. orbiculare, and C. albicans.
Miconazole 2% Cream

Definition

ChEBI: 1-[2-(2,4-dichlorobenzyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole is a member of the class of imidazoles that is 1-(2,4-dichlorophenyl)-2-(imidazol-1-yl)ethanol in which the hydroxyl hydrogen is replaced by a 2,4-dichlorobenzyl group. It is an ether, a member of imidazoles and a dichlorobenzene.

Indications

Miconazole (Monistat) is a broad-spectrum imidazole antifungal agent used in the topical treatment of cutaneous dermatophyte infections and mucous membrane Candida infections, such as vaginitis. Minimal absorption occurs from skin or mucous membrane surfaces. Local irritation to skin and mucous membranes can occur with topical use; headaches, urticaria, and abdominal cramping have been reported with treatment for vaginitis.

Manufacturing Process

Imidazole is reacted with ω-bromo-2,4-dichloroacetophenone and that product reduced with sodium borohydride.
A suspension of 10.3 parts of the α-(2,4-dichlorophenyl)imidazole-1-ethanol thus obtained and 2.1 parts of sodium hydride in 50 parts of dry tetrahydrofuran is stirred and refluxed for 2 hours. After this reaction time, the evolution of hydrogen is ceased. Then there are added successively 60 parts dimethylformamide and 8 parts of 2,4-dichlorobenzyl chloride and stirring and refluxing are continued for another 2 hours. The tetrahydrofuran is removed at atmospheric pressure. The dimethylformamide solution is poured onto water.
The product, 1-[2,4-dichloro-β-(2,4 -dichlorobenzyloxy)phenethyl]imidazole, is extracted with benzene. The extract is washed with water, dried, filtered and evaporated in vacuo. From the residual oily free base, the nitrate salt is prepared in the usual manner in 2-propanol by treatment with concentrated nitric acid, yielding, after recrystallization of the crude solid salt from a mixture of 2-propanol, methanol and diisopropyl ether, 1-[2,4-dichloro-β- dichlorobenzyloxy)phenethyl]imidazole nitrate; melting point 170.5°C.

brand name

M-Zole (Actavis); Monistat (Ortho-McNeil); Monistat (Personal Products); Monistat (Johnson & Johnson).

Therapeutic Function

Antifungal

Clinical Use

Antifungal agent

Synthesis

Miconazole, 1-[2,4-dichloro-|?-[(2,4-dichlorobenzyl)oxy]phenethyl]-imidazole (35.2.7), like ketoconazol, is synthesized from 2,4-dichlorophenacylbromide, which is reacted with imidazole to make 1-(2,4-dichlorobenzoylmethyl)-imidazole[2,4-dichloro-|?-(1-imidazolyl)-acetophenone] (35.2.5). Reducing the carbonyl group in this molecule with sodium borohydride gives 1-(2,4-dichlorophenyl)-3-(1-imidazolyl)-ethanol (35.2.6), and the hydroxyl group is alkylated by 2,4-dichlorobenzylbromide using a powerful base such as sodium hydride to make miconazole (35.2.7).

Synthesis_22916-47-8

Veterinary Drugs and Treatments

Miconazole is a broad spectrum imidazole antifungal agent with some antibacterial activity. Miconazole will penetrate the intact corneal epithelium. Topical miconazole therapy has been a favorite first choice agent for treatment of fungal keratitis in the horse by veterinary ophthalmologists for several years. Miconazole may be delivered by subconjunctival route, but with some local irritation, and topical use is the most commonly employed treatment method.

Veterinary Drugs and Treatments

Topical miconazole has activity against dermatophytes and yeasts; miconazole shampoos can be effective treatment for Malassezia dermatitis. Patients with severe, generalized infections may require systemic therapy. Lotions, sprays and creams are generally used for localized lesions associated with Malassezia or dermatophytes. See otic section for information on application for Malassezia otitis externa.
Topical miconazole products are generally ineffective (or minimally effective) when used alone for dermatophytosis; adjunctive systemic treatment is usually required.
Miconazole’s actions are a result of altering permeability of fungal cellular membranes and interfering with peroxisomal and mitochondrial enzymes, leading to intracellular necrosis. Miconazole products are fungicidal with repeated application.

Drug interactions

Potentially hazardous interactions with other drugs
Anticoagulants: effect of coumarins enhanced. Antidepressants: avoid concomitant use with reboxetine.
Antidiabetics: enhances hypoglycaemic effect of gliclazide and glipizide; concentration of sulphonylureas increased.
Antiepileptics: effect of fosphenytoin and phenytoin enhanced; possibly increased carbamazepine concentration.
Antihistamines: avoid with mizolastine, risk of ventricular arrhythmias.
Antimalarials: avoid with piperaquine with artenimol and artemether with lumefantrine
. Antipsychotics: increased risk of ventricular arrhythmias with pimozide - avoid; possibly increased concentration of quetiapine - avoid.
Antivirals: concentration of saquinavir possibly increased.
Ciclosporin: possibly increased ciclosporin concentration.
Ergot alkaloids: increased risk of ergotism with ergotamine and methysergide - avoid.
Sirolimus: concentration increased by miconazole.
Statins: possibly increased risk of myopathy with atorvastatin and simvastatin - avoid with simvastatin.
Tacrolimus: possibly increased tacrolimus concentration

Metabolism

Miconazole is metabolised in the liver to inactive metabolites; 10-20% of an oral dose is excreted in the urine as metabolites. About 50% of an oral dose may be excreted mainly unchanged in the faeces

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View Lastest Price from Miconazole manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Miconazole pictures 2024-01-02 Miconazole
22916-47-8
US $70.00 / kg 10kg 0.99 20tons Zibo Hangyu Biotechnology Development Co., Ltd
Miconazole pictures 2023-08-22 Miconazole
22916-47-8
US $10.00 / kg 1kg 99% 1000tons Henan Bao Enluo International TradeCo.,LTD
Miconazole pictures 2023-06-15 Miconazole
22916-47-8
US $77.00 / KG 1KG 99% 100kg Baoji Guokang Bio-Technology Co., Ltd.
  • Miconazole pictures
  • Miconazole
    22916-47-8
  • US $70.00 / kg
  • 0.99
  • Zibo Hangyu Biotechnology Development Co., Ltd
  • Miconazole pictures
  • Miconazole
    22916-47-8
  • US $10.00 / kg
  • 99%
  • Henan Bao Enluo International TradeCo.,LTD
  • Miconazole pictures
  • Miconazole
    22916-47-8
  • US $77.00 / KG
  • 99%
  • Baoji Guokang Bio-Technology Co., Ltd.

Miconazole Spectrum

LABOTEST-BB LT00255845 MONISTAT IV MICONAZOLE MICONAZOLE USP BASE MICONAZOLE FREE BASE MICONAZOLE MM(CRM STANDARD) MICONAZOLE USP(CRM STANDARD) MICONAZOLE(REAGENT / STANDARD GRADE) Daktarin IV Imidazole, 1-[2,4-dichloro-b-[(2,4-dichlorobenzyl)oxy]phenethyl]- (8CI) NSC 170986 1-[2-(2,4-Dichlorophenyl)-2-[(2,4-dichlorophenyl)methoxy]-1H-imidazole Miconazole (base and/or unspecified salts) 1-(2,4-Dichlorophenyl)-1-[(2,4-dichlorophenyl)methoxy]-2-(1H-imidazole-1-yl)ethane 1-[2,4-Dichloro-β-(2,4-dichlorobenzyloxy)phenethyl]-1H-imidazole 1-[2,4-Dichloro-β-[(2,4-dichlorobenzyl)oxy]phenethyl]-1H-imidazole Miconazol gel Miconazole gel Miconazole (200 mg) Miconozole Miconazole (Monistat) Isoconazole IMpurity C (Miconazole) 1-[2,4-DICHLORO-BETA-([2,4-DICHLOROBENZYL]OXY)-PHENETHYL]IMIDAZOLE 1-[2-(2,4-dichlorophenyl)-2-[(2,4-dichlorophenyl)methoxy]ethyl]-1h-imidazole 1-(2-(2,4-dichlorophenyl)-2-((2,4-dichlorophenyl)methoxy)ethyl)-imidazol 1-(2,4-dichloro-beta-((2,4-dichlorobenzyl)oxy)phenethyl)-imidazol 1-[2-[(2,4-Dichlorobenzyl)oxy]-2-(2,4-dichlorophenyl)ethyl]-1H-imidazole Imidazole, 1-(2-(2,4-dichlorophenyl)-2-((2,4-dichlorophenyl)methoxy)ethyl)- Imidazole, 1-(2,4-dichloro-beta-((2,4-dichlorobenzyl)oxy)phenethyl)- micronazol Minostate mjr1762 R 18134 r18134 Miconazol (RS)-1-(2-(2,4-DICHLOROBENZYLOXY)-2-(2,4-DICHLOROPHENYL)ETHYL)-1H-IMIDAZOLE Miconazole CRS Miconazole USP/EP/BP Miconazole (R18134) Miconazole (1443409) MiconazoleQ: What is Miconazole Q: What is the CAS Number of Miconazole Q: What is the storage condition of Miconazole Q: What are the applications of Miconazole MICONAZOLE BASE 1H-Imidazole, 1-[2-(2,4-dichlorophenyl)-2-[(2,4-dichlorophenyl)methoxy]ethyl]- (9CI) (1,2,4-dichlorophenyl)-1H-imidazole-1-Ethanol Miconazole Nitrate EP/CEP Miconazole Reference Standard 22916-47-8 Monistat