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Merck
CN

766399

2-Bromoisobutyric anhydride

95%

Synonym(s):

2-Bromo-2-methylpropanoic anhydride, ATRP initiator

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About This Item

Empirical Formula (Hill Notation):
C8H12Br2O3
CAS Number:
42069-15-8
Molecular Weight:
315.99
NACRES:
NA.23
PubChem Substance ID:
329767232
UNSPSC Code:
12162002
MDL number:
MFCD23704416

Key Documents

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Product Name

2-Bromoisobutyric anhydride, 95%

InChI

1S/C8H12Br2O3/c1-7(2,9)5(11)13-6(12)8(3,4)10/h1-4H3

SMILES string

CC(C)(Br)C(=O)OC(=O)C(C)(C)Br

InChI key

CHYAZMNKLHWVBP-UHFFFAOYSA-N

assay

95%

form

powder

mp

56-60 °C

Application

Highly effective difunctional initiator for atom transfer radical polymerization (ATRP).

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKCH5088
MKBM3925

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Xiujun Ren et al.
Journal of chromatography. A, 1618, 460904-460904 (2020-01-30)
A novel chiral stationary phase (CSP) was prepared through the reaction of surface-initiated atom transfer radical polymerization (ATRP) by the copolymerization of thermoresponsive N-isopropylacrylamide (NIPAM) and β-cyclodextrin (β-CD) on the silica beads for high performance liquid chromatography (HPLC). X-ray photoelectron
Shuaidong Huo et al.
Nature chemistry, 13(2), 131-139 (2021-01-31)
Pharmaceutical drug therapy is often hindered by issues caused by poor drug selectivity, including unwanted side effects and drug resistance. Spatial and temporal control over drug activation in response to stimuli is a promising strategy to attenuate and circumvent these

Articles

Functional Biomaterials Synthesized by Double-Head Polymerization Agents

Over the past two decades, the rapid advance of controlled living polymerization (CLP) techniques.

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