2257-35-4
Trichloroacrylic acid
CAS: 2257-35-4
Molecular Formula: C3HCl3O2
2257-35-4 - Names and Identifiers
2257-35-4 - Physico-chemical Properties
| Molecular Formula | C3HCl3O2 |
| Molar Mass | 175.4 |
| Density | 1.8624 (rough estimate) |
| Melting Point | 72-74°C |
| Boling Point | 249.25°C (rough estimate) |
| Flash Point | 78.996°C |
| Vapor Presure | 0.039mmHg at 25°C |
| BRN | 1754536 |
| pKa | pK1:1.15 (25°C) |
| Refractive Index | 1.5271 (estimate) |
2257-35-4 - Risk and Safety
| Risk Codes | 34 - Causes burns |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
| UN IDs | 3261 |
| Hazard Class | 8 |
| Packing Group | II |
2257-35-4 - Introduction
Trichloroacrylic acid is an organic compound with the chemical formula C3Cl3COOH. The following is an introduction to some of its properties, uses, methods and safety information:
Nature:
-Appearance: Colorless to slightly yellow crystal or solid powder at room temperature.
-Solubility: Soluble in water and organic solvents, such as alcohols and ethers.
-Stability: It is relatively stable under regular conditions, but it will decompose when heated, irradiated with ultraviolet light or exposed to strong oxidants.
Use:
-Chemical synthesis: Trichloroacrylic acid can be used to synthesize other organic compounds, such as polymers, chemical reagents and pharmaceutical intermediates.
-Chemical reaction: It can be used as an acid catalyst and reaction intermediate for organic synthesis reactions. For example, it is used as an important ligand for chlorinating agents and acid catalysts.
Method:
trichoroacrylic acid can be prepared by the following methods:
-Chlorination of trichloropropene gives trichloropropionyl chloride, which is then reacted with water to give Trichloroacrylic acid.
-Trichloroacetic acid (Trichloroacetic acid) is obtained by oxidation of trichloroethylene (Trichloroethene), and then Trichloroacrylic acid is obtained by decarboxylation reaction.
Safety Information:
-tricholoroacrylic acid is a corrosive substance that may cause irritation and damage to the eyes, skin and respiratory tract. Wear protective gloves, goggles and respiratory protection when using.
-Avoid contact with strong oxidants, strong acids, ammonia and other substances during storage and handling.
-Use and handle in a well-ventilated place and avoid inhalation, ingestion or contact with skin.
-In the case of accidental leaks, appropriate protective equipment and measures should be taken to avoid entering water sources, drainage systems and groundwater.
Please note that Trichloroacrylic acid is a chemical and must be handled with caution and in accordance with relevant regulations and safe operating procedures.
Nature:
-Appearance: Colorless to slightly yellow crystal or solid powder at room temperature.
-Solubility: Soluble in water and organic solvents, such as alcohols and ethers.
-Stability: It is relatively stable under regular conditions, but it will decompose when heated, irradiated with ultraviolet light or exposed to strong oxidants.
Use:
-Chemical synthesis: Trichloroacrylic acid can be used to synthesize other organic compounds, such as polymers, chemical reagents and pharmaceutical intermediates.
-Chemical reaction: It can be used as an acid catalyst and reaction intermediate for organic synthesis reactions. For example, it is used as an important ligand for chlorinating agents and acid catalysts.
Method:
trichoroacrylic acid can be prepared by the following methods:
-Chlorination of trichloropropene gives trichloropropionyl chloride, which is then reacted with water to give Trichloroacrylic acid.
-Trichloroacetic acid (Trichloroacetic acid) is obtained by oxidation of trichloroethylene (Trichloroethene), and then Trichloroacrylic acid is obtained by decarboxylation reaction.
Safety Information:
-tricholoroacrylic acid is a corrosive substance that may cause irritation and damage to the eyes, skin and respiratory tract. Wear protective gloves, goggles and respiratory protection when using.
-Avoid contact with strong oxidants, strong acids, ammonia and other substances during storage and handling.
-Use and handle in a well-ventilated place and avoid inhalation, ingestion or contact with skin.
-In the case of accidental leaks, appropriate protective equipment and measures should be taken to avoid entering water sources, drainage systems and groundwater.
Please note that Trichloroacrylic acid is a chemical and must be handled with caution and in accordance with relevant regulations and safe operating procedures.
Last Update：2024-04-09 15:17:56
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View History
2257-35-4
61788-89-4
2306247-65-2
异绿原酸 C
4-METHYLUMBELLIFERYL-BETA-D-CELLOBIOPYRANOSIDE
313339-35-4
十二醇
103285-22-9
61788-89-4
2306247-65-2
异绿原酸 C
4-METHYLUMBELLIFERYL-BETA-D-CELLOBIOPYRANOSIDE
313339-35-4
十二醇
103285-22-9