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HALOPROGIN

CAS No.
777-11-7
Chemical Name:
HALOPROGIN
Synonyms
polik;m1028;halotex;mycilan;mycanden;Fungaclor;haloprogin;NSC-100071;Haloproginum;HALOPROGIN (200 MG)
CBNumber:
CB4501419
Molecular Formula:
C9H4Cl3IO
Molecular Weight:
361.39
MDL Number:
MFCD00056358
MOL File:
777-11-7.mol
MSDS File:
SDS
Last updated:2026-01-22 22:14:22
Product description Number Pack Size Price
Haloprogin H1873 100MG $198
Haloprogin H103780 500mg $145
HALOPROGIN 95.00% API0008981 10MG $280.35
More product size

HALOPROGIN Properties

Melting point 113-114°
Boiling point 477.49°C (rough estimate)
Density 1.9350 (estimate)
form Solid
color White to off-white
FDA UNII AIU7053OWL
ATC code D01AE11

SAFETY

Risk and Safety Statements

Hazard Codes  Xn
Risk Statements  22-36/37/38
Safety Statements  26-36
RTECS  KO1225000
Toxicity LD50 in mice: >3 g/kg orally and s.c.; 510 mg/kg i.p. (Seki, 1963)

HALOPROGIN price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical H1873 Haloprogin 777-11-7 100MG $198 2025-07-31 Buy
TRC H103780 Haloprogin 777-11-7 500mg $145 2021-12-16 Buy
American Custom Chemicals Corporation API0008981 HALOPROGIN 95.00% 777-11-7 10MG $280.35 2021-12-16 Buy
Product number Packaging Price Buy
H1873 100MG $198 Buy
H103780 500mg $145 Buy
API0008981 10MG $280.35 Buy

HALOPROGIN Chemical Properties,Uses,Production

Chemical Properties

Light yellow or white crystal. Melting point 113-114 ℃, decomposed at 190 ℃. Soluble in ether, chloroform, ethyl acetate, methanol, ethanol and hot glacial acetic acid, almost insoluble in water. Has a special odor.

Originator

Halotex,Westwood,US,1972

Uses

Antibacterial.

Uses

Haloprogin is a topical antifungal agent used in the treatment of dermatophytic and monilial infections.

Definition

ChEBI: Haloprogin is an aromatic ether.

Indications

Haloprogin is used as an external drug for moderate dermatophyte infections (shingles), and it is effective for superficial candida infections. Synonyms of this drug are halotex, mycilan, micanden, and others.

Manufacturing Process

4.7 grams of 2,4,5-trichlorophenyl propargyl ether (MP 64° to 65°C) are added to an aqueous solution of cupro-ammonium complex salt which has been prepared by warming a mixture of 4.0 grams of cuprous chloride, 11.0 grams of ammonium carbonate and 20 cc of water to 50°C. The resulting admixture is shaken vigorously. The cuprous acetylide deposited is filtered, washed with water and suspended in 100 cc of water, and the suspension is mixed under agitation with a solution of 5.0 grams of iodine and 5.0 grams of potassium iodide in 15 cc of water. The mixture is stirred for a period of 1 hour. The precipitate is filtered, washed with water and extracted with ether. After the drying of the ethereal extract, the solvent is distilled off. Recrystallization of the residue from n-hexane gives about 5.6 grams of 2,4,5- trichlorophenyi iodopropargyl ether, MP 114° to 115°C.

brand name

Halotex (Westwood-Squibb).

Therapeutic Function

Antibacterial

General Description

3-Iodo-2-propynyl-2,4,5-trichlorophenyl ether (Halotex)crystallizes as white to pale yellow forms that are sparinglysoluble in water and very soluble in ethanol. It is an etherealderivative of a phenol. Haloprogin is used as a 1% cream forthe treatment of superficial tinea infections.
Formulations of haloprogin should be protected fromlight because the compound is photosensitive. Haloprogin isavailable as a solution and a cream, both in a 1% concentration.Haloprogin is probably not the first topical agent thatshould be recommended. Although the cure rates for topicalfungal infections are relatively high, they come at a highprice. The lesion typically worsens before it improves.Inflammation and painful irritation are common.

Synthesis

Haloprogin, 3-iodo-2-propinyl-2,4,5-trichlorophenyl ether (35.4.11), is synthesized by an iodide substitution using a mixture of iodine and potassium iodide and a cupric derivative of 2,4,5-trichlorophenylpropargyl ether (35.4.10), which is synthesized by a standard method from propargyl bromide and 2,4,5-trichlorophenol in the presence of sodium hydroxide.

Synthesis_777-11-7

HALOPROGIN Preparation Products And Raw materials

Global( 25)Suppliers
Supplier Tel Email Country ProdList Advantage
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49977 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 19282 58
TargetMol Chemicals Inc.
+1-781-999-5354; support@targetmol.com United States 39042 58
TargetMol Chemicals Inc.
+17819995354 marketing@targetmol.com United States 19964 58
Chongqing jooe co., ltd
+undefined86-15223382610 info@jooe.com China 15976 58
Shanghai Scibiotron Pharmaceutical Co., Ltd
+86-16621589600 contact@scibiotron.com China 5838 58
Shanghai Changyan Chem & Tech Co., Ltd. 021-20242659 18930833303 Sales@changyanchem.cn China 5001 55
Shanghai Rechem science Co., Ltd. 021-31433387 15618786686 sales@rechemscience.com China 2961 58
Shanghai alkynechem Co., Ltd. 086-021-15821262312 15821262312 info@alkynechem.com China 1993 58
Hebei Zhenjia new material Co., LTD 0319-5925599 13315915972 13313090628@163.com China 2916 58

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  • Mechanism and Toxicity of Haloprogin
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  • Mar 31,2022

View Lastest Price from HALOPROGIN manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Haloprogin pictures 2026-01-22 Haloprogin
777-11-7
US $156.00-247.00 / mg 98.18% 10g TargetMol Chemicals Inc.
HALOPROGIN (200 MG) USP/EP/BP pictures 2025-11-18 HALOPROGIN (200 MG) USP/EP/BP
777-11-7
US $1.10 / g 1g 99.9% 100 Tons Min Dideu Industries Group Limited
  • Haloprogin pictures
  • Haloprogin
    777-11-7
  • US $156.00-247.00 / mg
  • 98.18%
  • TargetMol Chemicals Inc.
1,2,.4-Trichloro-5-[(3-iodo-2-propynyl)oxy]benzene 2,4,5-trichlorophenyl-gamma-iodopropargylether 2,4,5-trichlorophenyliodopropargylether 3-iodo-2-propynyl2,4,5-trichlorophenylether ether,3-iodo-2-propynyl2,4,5-trichlorophenyl haloprogin halotex m1028 mycanden mycilan polik 1,2,4-trichloro-5-(3-iodoprop-2-ynoxy)benzene 1,2,4-trichloro-5-((3-iodoprop-2-yn-1-yl)oxy)benzene HALOPROGIN (200 MG) Fungaclor NSC-100071 HALOPROGIN (200 MG) USP/EP/BP Haloproginum Benzene, 1,2,4-trichloro-5-[(3-iodo-2-propyn-1-yl)oxy]- 777-11-7 C9H4Cl3IO