Miconazole
- Product Name
- 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;MICONAZOLE;NSC 170986;Miconozole
- CBNumber
- CB6493824
- Molecular Formula
- C18H14Cl4N2O
- Formula Weight
- 416.13
- MOL File
- 22916-47-8.mol
Miconazole Property
- 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).
- form
- Solid
- 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)
- 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)
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H413May cause long lasting harmful effects to aquatic life
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P273Avoid release to the environment.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- PHR1618
- Product name
- Miconazole
- Packaging
- 1g
- Price
- $121
- Updated
- 2024/03/01
- Product number
- 1443409
- Product name
- Miconazole
- Packaging
- 200mg
- Price
- $436
- Updated
- 2024/03/01
- Product number
- J60872
- Product name
- Miconazole, 99%
- Packaging
- 1g
- Price
- $18.65
- Updated
- 2024/03/01
- Product number
- J60872
- Product name
- Miconazole, 99%
- Packaging
- 5g
- Price
- $47.65
- Updated
- 2024/03/01
- Product number
- M1880000
- Product name
- Miconazole
- Purity
- European Pharmacopoeia (EP) Reference Standard
- Packaging
- m1880000
- Price
- $153
- Updated
- 2024/03/01
Miconazole Chemical Properties,Usage,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.
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).
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
- Product
- Miconazole 22916-47-8
- Price
- US $77.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 100kg
- Release date
- 2021-06-07
- Product
- Miconazole 22916-47-8
- Price
- US $70.00/kg
- Min. Order
- 10kg
- Purity
- 0.99
- Supply Ability
- 20tons
- Release date
- 2023-10-27
- Product
- Miconazole 22916-47-8
- Price
- US $10.00/kg
- Min. Order
- 1kg
- Purity
- 99%
- Supply Ability
- 1000tons
- Release date
- 2023-08-22