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Merck
CN

723185

1,1,1-Tris(2-bromoisobutyryloxymethyl)ethane

97%

Synonym(s):

3f-BiB, Trifunctional initiator

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About This Item

Empirical Formula (Hill Notation):
C17H27Br3O6
CAS Number:
Molecular Weight:
567.10
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
MDL number:
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InChI

1S/C17H27Br3O6/c1-14(2,18)11(21)24-8-17(7,9-25-12(22)15(3,4)19)10-26-13(23)16(5,6)20/h8-10H2,1-7H3

SMILES string

CC(C)(Br)C(=O)OCC(C)(COC(=O)C(C)(C)Br)COC(=O)C(C)(C)Br

InChI key

VLRDGSDXAISNJF-UHFFFAOYSA-N

assay

97%

form

powder

mp

54-60 °C

Application

Atom Transfer Radical Polymerization (ATRP) initiator for the creation of trifunctional polymers.
Polymerization will occur at three sites creating a three-arm star polymer.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

nwg

flash_point_f

>230.0 °F - closed cup

flash_point_c

> 110 °C - closed cup


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Coessens, V.; Pintauer, T.; Matyjaszewski, K.
Progress in Polymer Science, 36, 337-337 (2001)
Atom transfer radical polymerization.
K Matyjaszewski et al.
Chemical reviews, 101(9), 2921-2990 (2001-12-26)
"Green" atom transfer radical polymerization: from process design to preparation of well-defined environmentally friendly polymeric materials.
Nicolay V Tsarevsky et al.
Chemical reviews, 107(6), 2270-2299 (2007-05-29)

Articles

ATRP is a successful method for precise polymer synthesis with controlled molecular weights and high chain end functionalities.

Protocols

Polymerization via ATRP procedures demonstrated by Prof. Dave Haddleton's research group at the University of Warwick.

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