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Dibromoacetaldehyde is an organic compound with the chemical formula C2H2Br2O. It is a brominated acetaldehyde derivative, characterized by the presence of two bromine atoms attached to the carbonyl group. DIBROMOACETALDEHYDE is known for its reactivity and is often utilized in various chemical and analytical applications due to its unique properties.

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  • 3039-13-2 Structure
  • Basic information

    1. Product Name: DIBROMOACETALDEHYDE
    2. Synonyms: DIBROMOACETALDEHYDE;Acetaldehyde, dibroMo-;2,2-dibromoacetaldehyde
    3. CAS NO:3039-13-2
    4. Molecular Formula: C2H2Br2O
    5. Molecular Weight: 201.84
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3039-13-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 136.3°Cat760mmHg
    3. Flash Point: 68.7°C
    4. Appearance: /
    5. Density: 2.357g/cm3
    6. Vapor Pressure: 7.41mmHg at 25°C
    7. Refractive Index: 1.541
    8. Storage Temp.: Hygroscopic, Refrigerator, under inert atmosphere
    9. Solubility: DMSO (Very Slightly), Methanol (Slightly, Heated)
    10. Stability: Extremely Moisture Sensitive, Hygroscopic
    11. CAS DataBase Reference: DIBROMOACETALDEHYDE(CAS DataBase Reference)
    12. NIST Chemistry Reference: DIBROMOACETALDEHYDE(3039-13-2)
    13. EPA Substance Registry System: DIBROMOACETALDEHYDE(3039-13-2)
  • 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: 3039-13-2(Hazardous Substances Data)

3039-13-2 Usage

Uses

Used in Analytical Chemistry:
Dibromoacetaldehyde is used as a reagent in analytical chemistry for the determination of haloacetaldehydes in treated water. It plays a crucial role in micro liquid-liquid extraction combined with large volume injection gas chromatography-mass spectrometry (GC-MS). This application is essential for monitoring and ensuring the quality of treated water, as haloacetaldehydes can be harmful to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 3039-13-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,3 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3039-13:
(6*3)+(5*0)+(4*3)+(3*9)+(2*1)+(1*3)=62
62 % 10 = 2
So 3039-13-2 is a valid CAS Registry Number.
InChI:InChI=1/C2H2Br2O/c3-2(4)1-5/h1-2H

3039-13-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dibromoacetaldehyde

1.2 Other means of identification

Product number -
Other names DIBROMOACETALDEHYDE

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:3039-13-2 SDS

3039-13-2Relevant articles and documents

REACTION OF 2-TERT-BUTOXY-4,5-BENZO-1,3,2-DIOXAPHOSPHOLANE WITH TRIBROMOACETALDEHYDE

Sinyashina, T. N.,Mironov, V. F.,Ofitserov, E. N.,Konovalova, I. V.,Pudovik, A. N.

, p. 1755 - 1757 (2007/10/02)

The reaction of 2-tert-butoxy-4,5-benzo-1,3,2-dioxaphospholane with tribromoacetaldehyde proceeds by initial halophilic attack on the bromine atom, leading to a product with retention of the P-Br bond (pyrocatechol bromophosphate) and an anion exchange product (pyrocatechol dibromovinylphosphate), and by initial attack at the carbon atom of the C=O group, which is accompanied by the elimination of isobutylene to form an α-hydroxyphosphonate.

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