420-97-3

Basic information

• Product Name: 1,2-DICHLORO-2-FLUOROPROPANE
• Synonyms: 1,2-Dichlor-2-fluorpropan;H-FCKW-261;Propane, 1,2-dichloro-2-fluoro-;Propane,1,2-dichloro-2-fluoro-;2-FLUORO-1,2-DICHLOROPROPANE;1,2-DICHLORO-2-FLUOROPROPANE;HCFC-216BA;1,2-Dichloro-2-fluoropropane (HCFC-216ba), tech
• CAS NO: 420-97-3
• Molecular Formula: C₃H₅Cl₂F
• Molecular Weight: 130.98
• EINECS: 206-999-1
• Product Categories: refrigerants
• Mol File: 420-97-3.mol

Chemical Properties

• Melting Point: -92,5°C
• Boiling Point: 88-89°C
• Flash Point: 3.6°C
• Appearance: /
• Density: 1,412 g/cm3
• Vapor Pressure: 68.2mmHg at 25°C
• Refractive Index: 1.2618
• CAS DataBase Reference: 1,2-DICHLORO-2-FLUOROPROPANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-DICHLORO-2-FLUOROPROPANE(420-97-3)
• EPA Substance Registry System: 1,2-DICHLORO-2-FLUOROPROPANE(420-97-3)

Safety Data

• Hazard Codes: F
• Statements: 10
• Safety Statements: 16
• RIDADR: 1993
• Hazardous Substances Data: 420-97-3(Hazardous Substances Data)

Usage

Uses

Used in Chemical Production:
1,2-Dichloro-2-fluoropropane is used as an intermediate in the production of other chemicals, playing a crucial role in the synthesis of various compounds for different applications.
Used in Solvent Applications:
1,2-DICHLORO-2-FLUOROPROPANE serves as a solvent in various industrial processes, where its unique properties facilitate the dissolution of certain substances, aiding in chemical reactions or material processing.
Used in Refrigeration Industry:
1,2-Dichloro-2-fluoropropane is utilized as a refrigerant in cooling systems, taking advantage of its thermodynamic properties to transfer heat and achieve cooling effects.
It is important to handle 1,2-dichloro-2-fluoropropane with care due to its hazardous nature, ensuring proper safety measures are in place to minimize risks to human health and the environment.

InChI:InChI=1/C3H5Cl2F/c1-3(5,6)2-4/h2H2,1H3

Upstream product

• 78-88-6 2,3-Dichloroprop-1-ene 
• 563-54-2 1,2-dichloro-propene 
• 1184-60-7 2-fluoropropene 
• 7664-39-3 hydrogen fluoride 
• 7637-07-2 boron trifluoride 
• 420-45-1 2,2-difluoropropane 

Downstream Products

• 1184-60-7 2-fluoropropene 
• 422-81-1 1,1,1,2,3,3,3-heptachloro-2-fluoro-propane 
• 3175-24-4 1,1,2-trichloro-2-fluoro-propane 
• 3175-25-5 1,1,1,2-tetrachloro-2-fluoro-propane 
• 3175-26-6 1,1,2,3-tetrachloro-2-fluoropropane 
• 421-94-3 1,1,1,2,3-pentachloro-2-fluoro-propane 
• 422-40-2 1,1,1,2,3,3-hexachloro-2-fluoro-propane 

Relevant articles and documents

PROCESSES FOR PRODUCING 2-CHLORO-1,1,1,2-TETRAFLUOROPROPANE AND 2,3,3,3-TETRAFLUOROPROPENE

To provide processes for efficiently and economically producing 2-chloro-1,1,1,2-tetrafluoropropane (R244bb) and 2,3,3,3-tetrafluoropropene (R1234yf) in an industrially practical manner. A process for producing 2-chloro-1,1,1,2-tetrafluoropropane, which comprises a chlorination step of reacting 1,2-dichloro-2-fluoropropane and chlorine in the presence of a solvent under irradiation with light to obtain 1,1,1,2-tetrachloro-2-fluoropropane, and a fluorination step of reacting the 1,1,1,2-tetrachloro-2-fluoropropane obtained in the chlorination step and hydrogen fluoride in the presence of a catalyst to obtain 2-chloro-1,1,1,2-tetrafluoropropane, and a process for producing 2,3,3,3-tetrafluoropropene, which comprises dehydrochlorinating it in the presence of a catalyst.

Fluorination process using hydrogen fluoride-containing fluorinating agents

Fluorination processes using hydrogen fluoride-containing fluorinating agents that are safely and easily handled, transported, and stored and that also exhibit good reactivity are provided. More particularly, the invention provides processes for producing fluorinated products using fluorinating agents comprising hydrogen fluoride and a carrier that may be an acid salt or a water-soluble polymer.

REACTION OF ALKANES, ETHERS AND ALIPHATIC KETONES WITH THE SF4-HF-Cl2 SYSTEM

The reaction of alkanes, ethers, and aliphatic ketones with the SF4-HF-Cl2 system takes place through formation of unsaturated compounds followed by addition of the chloride and fluoride ions.The presence of sulfur tetrafluoride in the rection mixture pro