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CAS

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62127-47-3

2,2,3-TRIBROMOBUTANE, with the chemical formula C4H7Br3, is a colorless liquid that exhibits limited solubility in water. As a chemical intermediate, it plays a significant role in the synthesis of various other chemicals. However, it is recognized as a hazardous substance due to its potential to cause harm if ingested, inhaled, or absorbed through the skin, and it can lead to respiratory and skin irritations, as well as being harmful to aquatic life.

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  • 62127-47-3 Structure

  • Basic information

    1. Product Name: 2,2,3-TRIBROMOBUTANE
    2. Synonyms: 2,2,3-TRIBROMOBUTANE;2,2,3-tribromo-butan;tribromobutane;Butane, 2,2,3-tribromo-;Inchi=1/C4H7br3/C1-3(5)4(2,6)7/H3H,1-2h
    3. CAS NO:62127-47-3
    4. Molecular Formula: C4H7Br3
    5. Molecular Weight: 294.81
    6. EINECS: 263-424-7
    7. Product Categories: N/A
    8. Mol File: 62127-47-3.mol

  • Chemical Properties

    1. Melting Point: 1.85°C
    2. Boiling Point: 86 °C / 14mmHg
    3. Flash Point: 110 °C
    4. Appearance: /
    5. Density: 2.18
    6. Refractive Index: 1.5610 to 1.5640
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,2,3-TRIBROMOBUTANE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2,3-TRIBROMOBUTANE(62127-47-3)
    11. EPA Substance Registry System: 2,2,3-TRIBROMOBUTANE(62127-47-3)

  • 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: 62127-47-3(Hazardous Substances Data)

62127-47-3 Usage

Uses

Used in Chemical Synthesis:
2,2,3-TRIBROMOBUTANE is used as a chemical intermediate for the synthesis of other chemicals. Its reactivity with oxidizing agents makes it a valuable component in the production of various compounds.
Used in Industrial Applications:
In the industrial sector, 2,2,3-TRIBROMOBUTANE is utilized in specific processes that require its unique chemical properties. However, due to its hazardous nature, strict safety measures and handling protocols are essential to mitigate risks to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 62127-47-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,2 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62127-47:
(7*6)+(6*2)+(5*1)+(4*2)+(3*7)+(2*4)+(1*7)=103
103 % 10 = 3
So 62127-47-3 is a valid CAS Registry Number.

62127-47-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3-TRIBROMOBUTANE

1.2 Other means of identification

Product number -
Other names Butane,2,2,3-tribromo

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:62127-47-3 SDS

62127-47-3Relevant articles and documents

A reinvestigation of the vapor phase bromination of 2-bromobutane

Tanner, Dennis D.,Ruo, Tomoki C. S.,Kosugi, Yoshio,Potter, Alan

, p. 2310 - 2316 (2007/10/02)

The soltuion phase photobromination of 2-bromobutane yields 2,2-dibromobutane, meso-2,3-dibromobutane, dl-2,3-dibromo-dibromobutane, small amounts of 1,2-dibromobutane, and 2,2,3-tribromobutane.However, in the corresponding vapor phase bromination these products appear along with other polybrominated products.The yield of these polybromides increases with temperature.The increase in yield of the polyhalogenated materials is rationalized by considering the thermal instabilty of the β-bromoalkyl radical, which eliminates a bromine atom to form the corresponding alkene.It is demonstrated that in the vapor phase allylic bromination competes succesfully with bromine addition.Reaction schemes are suggested to explain the formation of polybromides.An explanation is also offered for the dicrepancy between these results and those of previously reported vapor phase work.

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