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1‑Bromo‑3,5‑dichlorobenzene
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Product Details
BASIC INFORMATION:
Product Name: 1‑Bromo‑3,5‑dichlorobenzene
Chemical Formula: C₆H₃BrCl₂
Synonym: 3,5Dichlorobromobenzene, 3,5Dichloro1bromobenzene
CAS: 19752-55-7
HS Code: 29039990
Molecular Weight: 225.90
Einecs: 243-270-7
Structural Formula:

Brief Description:
1Bromo3,5dichlorobenzene is a white to slightly yellow crystalline solid with high symmetry. It is widely used in the synthesis of dyes, pharmaceuticals, and pesticides.
TECHNICAL INDICATORS:
Items | Result |
Appearance | White to slightly yellow crystals |
Density | 1.744 g/cm³ |
Vapor pressure | 0.0998 mmHg (25°C) |
Purity (%) | ≥99.5% |
APPLICATIONS:
1. Pharmaceutical intermediate: Used in the synthesis of antifungal drugs (e.g., benzene ring analogues of miconazole and econazole) and antiparasitic agents. Example: Ullmann coupling to form a diaryl ether structure for enhanced antifungal activity.
2. Pesticide intermediate: Used to prepare diclosulam‑type herbicides and phenylpyrazole insecticides (e.g., chlorine analogues of fipronil).
3. Dye intermediate: Acts as the diazo component for azo dyes to produce bright yellow to red disperse dyes, such as certain Disperse Yellow series.
4. Flame retardant feedstock: Utilizes bromine‑chlorine synergy; can be used to synthesize bromine‑chlorine flame retardants, e.g., alternatives to tetrabromobisphenol A.
STORAGE CONDITIONS:
1. Store in a cool, dry, well‑ventilated area.
2. Keep container tightly closed; store in a cool, dry, ventilated place.
3. Separate from oxidizing agents and combustible materials – do not mix storage.
4. Ventilation systems should be equipped with static electricity grounding.
5. The storage area should be equipped with spill containment and appropriate collection materials.
PACKAGE:
1. Tightly sealed container.
2. Other packaging forms available upon request.
CHEMICAL PROPERTIES:
Melting point: 73–75°C, boiling point: 232°C (757 mmHg). Solid crystals, soluble in hot ethanol, toluene, and dichloromethane. The bromine atom is more reactive than the chlorine atoms, allowing selective palladium‑catalyzed coupling reactions. Dust is irritating; avoid inhalation during handling.
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