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CAS

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422-01-5

3-Bromo-1,1,1,2,2-pentafluoropropane is a halogenated hydrocarbon with the chemical formula C3HBrF5. It is a colorless, volatile liquid at room temperature and is characterized by its high electronegativity and low reactivity. 3-BroMo-1,1,1,2,2-pentafluoropropane is primarily used as a refrigerant, fire suppressant, and blowing agent in various industrial applications. Due to its low global warming potential and non-ozone-depleting properties, it is considered an environmentally friendly alternative to traditional chlorofluorocarbons (CFCs) and hydrochlorofluorocarbons (HCFCs). However, it is important to note that 3-bromo-1,1,1,2,2-pentafluoropropane is still a potent greenhouse gas, and its use should be carefully managed to minimize its impact on climate change.

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  • 422-01-5 Structure

  • Basic information

    1. Product Name: 3-BroMo-1,1,1,2,2-pentafluoropropane
    2. Synonyms: 3-BroMo-1,1,1,2,2-pentafluoropropane
    3. CAS NO:422-01-5
    4. Molecular Formula: C3H2BrF5
    5. Molecular Weight: 212.943996
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 422-01-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 45.2°C at 760 mmHg
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.8217 (rough estimate)
    6. Vapor Pressure: 366mmHg at 25°C
    7. Refractive Index: 1.4820 (estimate)
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-BroMo-1,1,1,2,2-pentafluoropropane(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-BroMo-1,1,1,2,2-pentafluoropropane(422-01-5)
    12. EPA Substance Registry System: 3-BroMo-1,1,1,2,2-pentafluoropropane(422-01-5)

  • 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: 422-01-5(Hazardous Substances Data)

422-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 422-01-5 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 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 422-01:
(5*4)+(4*2)+(3*2)+(2*0)+(1*1)=35
35 % 10 = 5
So 422-01-5 is a valid CAS Registry Number.
InChI:InChI=1/C3H2BrF5/c4-1-2(5,6)3(7,8)9/h1H2

422-01-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-1,1,1,2,2-pentafluoropropane

1.2 Other means of identification

Product number -
Other names 2,2,3,3,3-Pentafluoropropyl bromide

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:422-01-5 SDS

422-01-5Relevant articles and documents

HYDROFLUOROOLEFINS AND METHODS OF USING SAME

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Page/Page column 18-19, (2020/07/14)

A hydrofluoroolefin compound represented by the following general formula (II): Formula (II) where Rf is a linear, branched, or cyclic perfluoroalkyl group having 1-6 carbon atoms, and optionally comprises at least one catenated heteroatom selected from nitrogen or oxygen; n is 0 or 1; X is Cl or Br; with the following proviso: when Rf is CF3, then n is 1.

Catalytical production processes for making hydrohalopropanes and hydrofluorobutanes

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Page/Page column 4, (2008/06/13)

A process is disclosed for making hydrohalopropanes or hydrofluorobutanes. The process involves reacting a hydrofluoromethane with a fluoroolefin in the presence of an aluminum catalyst to produce a hydrohalopropane or a hydrofluorobutane. The hydrofluoromethane is CH2F2 or CH3F. The fluoroolefin is CF2═CF2, ClFC═CF2, or CF3CF═CF2.

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