Thermo Scientific Chemicals

2-Bromoisobutyryl bromide, 97%, Thermo Scientific Chemicals

Catalog number: B24249.22
100 g, Each
Thermo Scientific Chemicals

2-Bromoisobutyryl bromide, 97%, Thermo Scientific Chemicals

Catalog number: B24249.22
100 g, Each
Quantity
Informational:Informational:This chemical may require us to obtain additional information for our regulatory and chemical compliance records. If required, we will contact you for this information once your order is placed.
Catalog number: B24249.22
also known as B24249-22
Price (EUR)
Price: 40,70
Online price: 36,63
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Chemical Identifiers

CAS
20769-85-1
IUPAC Name
2-bromo-2-methylpropanoyl bromide
Molecular Formula
C4H6Br2O
InChI Key
YOCIJWAHRAJQFT-UHFFFAOYSA-N
SMILES
CC(C)(Br)C(Br)=O
Appearance (Color)
Clear colorless to pale yellow or pale pink
Form
Liquid
Assay (GC)
≥96.0%
Refractive Index
1.5075-1.5125 @ 20?C

Description

2-Bromoisobutyryl bromide is used to prepare N-protected halodienamide, which provides four- and five-membered lactams in the presence of copper(I) and a tertiary amine. Further, it is used as atom transfer radical polymerization(ATRP) initiator for functionalization of hydroxyl groups present on the surface of graphene oxide. It is also used in preparation of polycaprolactone macroinitiators through reaction with oligomeric caprolactone diol and mesoporous silica nanoparticles with ATRP initiator anchored on the exterior surface.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2-Bromoisobutyryl bromide is used to prepare N-protected halodienamide, which provides four- and five-membered lactams in the presence of copper(I) and a tertiary amine. Further, it is used as atom transfer radical polymerization(ATRP) initiator for functionalization of hydroxyl groups present on the surface of graphene oxide. It is also used in preparation of polycaprolactone macroinitiators through reaction with oligomeric caprolactone diol and mesoporous silica nanoparticles with ATRP initiator anchored on the exterior surface.

Solubility
Miscible with acetone and carbon disulfide.

Notes
Moisture sensitive. Incompatible with strong oxidizing agents and strong alkalis.
RUO – Research Use Only

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    Safety and Handling


    Classification of the substance or mixture
    CLP classification - Regulation(EC) No 1272/2008
    Acute oral toxicity
    Category 4
    Skin Corrosion/Irritation
    Category 1
    Serious Eye Damage/Eye Irritation
    Category 1
    Skin Sensitization
    Category 1
    Germ Cell Mutagenicity
    Category 1B
    Label Elements
    Signal Word

    Danger

    Hazard Statements

    H302 - Harmful if swallowed

    H314 - Causes severe skin burns and eye damage

    H317 - May cause an allergic skin reaction

    H340 - May cause genetic defects

    Precautionary Statements

    P280 - Wear protective gloves/protective clothing/eye protection/face protection

    P301 + P330 + P331 - IF SWALLOWED: Rinse mouth. Do NOT induce vomiting

    P303 + P361 + P353 - IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water or shower

    P305 + P351 + P338 - IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing

    P310 - Immediately call a POISON CENTER or doctor/physician

    Additional EU labelling

    Restricted to professional users