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2-Chloro-1,1,1,2-tetrafluoropropane, also known as R-124, is a halogenated hydrocarbon with the chemical formula C3HClF4. It is a colorless, volatile liquid at room temperature and is used primarily as a refrigerant and as a blowing agent in the production of foams. R-124 is a member of the hydrochlorofluorocarbon (HCFC) family, which are considered to be less harmful to the ozone layer compared to chlorofluorocarbons (CFCs). However, it still has a global warming potential, and its use is being phased out in favor of more environmentally friendly alternatives due to its contribution to climate change.

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  • 421-73-8 Structure
  • Basic information

    1. Product Name: 2-Chloro-1,1,1,2-tetrafluoropropane
    2. Synonyms: 2-Chloro-1,1,1,2-tetrafluoropropane;1,1,1,2-Tetrafluoro-2-chloropropane
    3. CAS NO:421-73-8
    4. Molecular Formula: C3H3ClF4
    5. Molecular Weight: 150.5
    6. EINECS: N/A
    7. Product Categories: refrigerants
    8. Mol File: 421-73-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 11.95°C (rough estimate)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.2432 (estimate)
    6. Refractive Index: 1.3063 (estimate)
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Chloro-1,1,1,2-tetrafluoropropane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Chloro-1,1,1,2-tetrafluoropropane(421-73-8)
    11. EPA Substance Registry System: 2-Chloro-1,1,1,2-tetrafluoropropane(421-73-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 421-73-8(Hazardous Substances Data)

421-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 421-73-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,2 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 421-73:
(5*4)+(4*2)+(3*1)+(2*7)+(1*3)=48
48 % 10 = 8
So 421-73-8 is a valid CAS Registry Number.

421-73-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name HCFC-244bb

1.2 Other means of identification

Product number -
Other names 2?chloro-1,1,1,2-tetrafluoropropane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:421-73-8 SDS

421-73-8Relevant articles and documents

PROCESS FOR PRODUCING FLUORINE-CONTAINING OLEFIN

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Paragraph 0090-0093; 0097, (2016/12/22)

In the production of fluorine-containing olefins using a chlorine-containing alkane or a chlorine-containing alkene as a starting material, a process for producing a plurality of useful fluorine-containing olefins with high selectivity using the same raw material, the same equipment, and the same conditions is provided. The present invention provides a process for producing fluorine-containing olefins, the process comprising reacting a chlorine-containing compound represented by a specific formula and anhydrous hydrogen fluoride in the presence of oxidative gas and a fluorination catalyst, wherein the fluorination catalyst is a catalyst in which at least one metal element M selected from the group consisting of Group VIII and Group IX is present together with chromium. This production process can simultaneously produce two or more fluorine-containing olefin compounds, including HFO-1234yf and HFO-1234ze, with high selectivity.

REACTOR FOR LIQUID PHASE FLUORINATION REACTIONS

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Paragraph 0088, (2015/09/22)

The present invention relates to a hydrofluorinating process which comprises reacting a fluoroolefin with hydrogen fluoride in the liquid phase in the presence of a hydrofluorination catalyst in the reaction zone of a reactor, said reactor comprised of a reactor body having a length to diameter ratio of about 2:1 or greater; a stirred reaction zone containing said hydrofluorination catalyst, which may be prepared in situ, at least one inlet for supplying said hydrogen fluoride and fluoroolefin to the reaction zone and at least one outlet for recovering said fluoroalkane, said stirrer disposed in the reaction zone and comprising a plurality of blades fixedly attached to shaft drivable by a motor, said blades extending from about the bottom of the reaction zone to about the top of the reaction zone and said shaft extending on a longitudinal axis from the bottom of the reactor to the top of the reactor, said stirrer being rotated at a speed sufficient to promote a swirling of the liquid to effect the occurrence of hydrofluorination reaction and minimize overfluorination. The present invention also relates to said hydrofluorination reactor.

Compositions

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Paragraph 0109; 0110; 0111; 0112, (2013/09/12)

A composition comprising HCFO-1233xf and at least one additional compound selected from the group consisting of HCFO-1233zd, HCFO-1232xd, HCFO-1223xd, HCFC-253fb, HCFC-233ab, HFO-1234yf, HFO-1234ze, ethylene, HFC-23, CFC-13, HFC-143a, HFC-152a, HFO-1243zf, HFC-236fa, HCO-1130, HCO-1130a, HFO-1336, HCFC-244bb, HCFC-244db, HFC-245fa, HFC-245cb, HCFC-133a, HCFC-254fb, HCFC-1131, HCFO-1242zf, HCFO-1223xd, HCFC-233ab, HCFC-226ba, and HFC-227ca.

CATALYTIC FLUORINATION PROCESS OF MAKING HYDROHALOALKANE

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Paragraph 0072; 0073, (2013/05/23)

The present disclosure provides a fluorination process which involves reacting a hydrohaloalkene of the formula RfCCl=CH2 with HF in a reaction zone in the presence of a fluorination catalyst selected from the group consisting of TaF5 and TiF4 to produce a product mixture containing a hydrohaloalkane of the formula RfCFClCH3, wherein Rf is a perfluorinated alkyl group.

METHOD FOR PRODUCING TETRAFLUOROPROPENES

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Page/Page column 4, (2011/11/12)

The current invention relates to a process for making a tetrafluoropropene using a tetrafluorochloropropane and/or a pentafluoropropane as starting or intermediate reagents. More specifically, though not exclusively, the present invention relates to a novel method for preparing a tetrafluoropropene by dehydrohalogenating a starting or intermediate tetrafluorochloropropane and/or pentafluoropropane material in the presence of a caustic solution at a temperature range greater than 40° C. and less than or equal to 80° C.

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

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Page/Page column 5-6, (2011/10/12)

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.

HYDROFLUORINATION OF 2-CHLORO-3,3,3-TRIFLUOROPROPENE TO 2-CHLORO-1,1,1,2-TETRAFLUOROPROPANE WITH CATALYSTS OF SBCL3, SBCL5, SBF5, TICL4, SNCL4, CR2O3 AND FLUORINATED CR2O3

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Page/Page column 3-7, (2009/07/25)

A process for making 2-chloro-1,1,1,2-tetrafluoropropane comprising hydrofluorinating 2-chloro-3,3,3-trifluoropropene in the presence of a catalyst selected from the group consisting of: SbCl3, SbCl5, SbF5, TiCl4, SnCl4, Cr2O3, and fluorinated Cr2O3.

GAS PHASE SYNTHESIS OF 2,3,3,3-TETRAFLUORO-1-PROPENE FROM 2-CHLORO-3,3,3-TRIFLUORO-1-PROPENE

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Page/Page column 2, (2009/05/28)

A multi-step process for preparing 2,3,3,3-tetrafluoro-1-propene comprising the steps of (a) contacting a starting material comprising 2-chloro-3,3,3-trifluoro-1-propene with hydrogen fluoride in the presence of activated first catalyst selected from the group consisting of antimony-halides, iron-halides, titanium halides, and tin-halides, to produce an intermediate composition; and (b) contacting said intermediate composition with a second catalyst of activated carbon to produce a final product comprising 2,3,3,3-tetrafluoro-1-propene.

Hydrofluorination of 2-chloro-3,3,3-trifluoropropene to 2-chloro-1,1,1,2-tetrafluoropropane

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Page/Page column 6-9, (2009/08/14)

A process for making 2-ch1oro-1,1,1,2-tetrafluoropropane comprising hydrofluorinating 2-chloro-3,3,3-trifluoropropene in the presence of a catalyst selected from the group consisting of: SbC13, SbCl5, SbF5, TiCl4, SnCl4, Cr2O3, and fluorinated Cr2O3.

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