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2,5-Dichlorophenol
[CAS# 583-78-8]

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Complete supplier list of 2,5-Dichlorophenol
Identification
Classification Chemical pesticide >> Herbicide >> Herbicide intermediate
Name 2,5-Dichlorophenol
Synonyms 2,5-DCP
Molecular Structure CAS # 583-78-8, 2,5-Dichlorophenol, 2,5-DCP
Molecular Formula C6H4Cl2O
Molecular Weight 163.00
CAS Registry Number 583-78-8
EC Number 209-520-4
SMILES C1=CC(=C(C=C1Cl)O)Cl
Properties
Density 1.5±0.1 g/cm3, Calc.*
Melting point 54-58 ºC
Index of Refraction 1.594, Calc.*
Boiling Point 214.6±20.0 ºC (760 mmHg), Calc.*, 211 ºC
Flash Point 100.0±15.8 ºC, Calc.*, 100 ºC
Water solubility 3 g/L (20 ºC)
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol symbol symbol   GHS05;GHS07;GHS09 Danger    Details
Hazard Statements H302-H314-H315-H318-H319-H411    Details
Precautionary Statements P260-P264-P264+P265-P270-P273-P280-P301+P317-P301+P330+P331-P302+P352-P302+P361+P354-P304+P340-P305+P351+P338-P305+P354+P338-P316-P317-P321-P330-P332+P317-P337+P317-P362+P364-P363-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Skin corrosionSkin Corr.1BH314
Serious eye damageEye Dam.1H318
Eye irritationEye Irrit.2AH319
SDS Available
up Discovory and Applicatios
2,5-Dichlorophenol is an aromatic compound with the molecular formula C6H4Cl2O, characterized by two chlorine substituents on the benzene ring at the 2 and 5 positions. This compound belongs to a class of chemicals known as chlorophenols, which are widely recognized for their antibacterial and antifungal properties. The discovery of 2,5-dichlorophenol can be traced back to the early 20th century, as chemists explored the synthesis and application of chlorinated derivatives of phenol.

The synthesis of 2,5-dichlorophenol typically involves the chlorination of phenol in the presence of a suitable chlorinating agent, such as chlorine gas or sulfuryl chloride. The position of the chlorine atoms is determined by the reaction conditions, resulting in the selective formation of the 2,5-isomer. Researchers initially sought to investigate the biological properties of chlorinated phenols, leading to the exploration of 2,5-dichlorophenol for potential applications.

One of the primary applications of 2,5-dichlorophenol is in the field of biocides and disinfectants. Its effective antimicrobial properties make it suitable for use in various formulations aimed at controlling microbial growth in different settings, including industrial, agricultural, and household environments. The compound acts by disrupting microbial cell membranes and interfering with metabolic processes, providing an effective means of sanitation.

In addition to its use as a biocide, 2,5-dichlorophenol has found applications in the synthesis of other chemical compounds. It serves as a valuable intermediate in the production of agrochemicals, such as herbicides and fungicides, which leverage its chlorinated structure to enhance biological activity and effectiveness. Furthermore, 2,5-dichlorophenol is utilized in the manufacture of dyes and pigments, where its chlorinated aromatic nature contributes to the stability and color properties of the final products.

The compound has also attracted attention in environmental research due to its persistence and potential ecological impact. As a byproduct of various industrial processes and a component in some formulations, 2,5-dichlorophenol can be released into the environment, necessitating studies on its fate and degradation pathways. Regulatory agencies have established guidelines for its safe use, emphasizing the importance of monitoring and managing its environmental presence.

In recent years, 2,5-dichlorophenol has been the subject of studies investigating its potential health effects. Research has indicated that, while it possesses useful antimicrobial properties, exposure to high concentrations can pose risks to human health, particularly regarding skin irritation and potential endocrine-disrupting effects. Consequently, ongoing research aims to elucidate the toxicological profiles of chlorophenols, including 2,5-dichlorophenol, to ensure safe handling and usage in various applications.

In summary, 2,5-dichlorophenol is a significant chlorinated aromatic compound with diverse applications in biocides, agrochemicals, and dye production. Its discovery and subsequent development highlight the interplay between chemistry and practical applications in addressing various industrial and environmental challenges.
Market Analysis Reports
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