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Sigma-Aldrich

N-tert-Butyl-O-[1-[4-(chloromethyl)phenyl]ethyl]-N-(2-methyl-1-phenylpropyl)hydroxylamine

Synonym(s):

Alkoxyamine NMP initiator

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About This Item

Empirical Formula (Hill Notation):
C23H32ClNO
CAS Number:
Molecular Weight:
373.96
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

form

solid

mp

43-47 °C

storage temp.

−20°C

SMILES string

CC(C)C(N(OC(C)c1ccc(CCl)cc1)C(C)(C)C)c2ccccc2

InChI

1S/C23H32ClNO/c1-17(2)22(21-10-8-7-9-11-21)25(23(4,5)6)26-18(3)20-14-12-19(16-24)13-15-20/h7-15,17-18,22H,16H2,1-6H3

InChI key

WZYBDTCNEIULNZ-UHFFFAOYSA-N

General description

For a synthetic protocol using NMP initiators, contributed by Prof. Karen Wooley, please visit our technology spotlight.

Pictograms

Flame over circleCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Ox. Sol. 3 - Skin Corr. 1B

Storage Class Code

5.1B - Oxidizing hazardous materials

WGK

WGK 3

Flash Point(F)

>230.0 °F - closed cup

Flash Point(C)

> 110 °C - closed cup


Certificates of Analysis (COA)

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Articles

Block copolymer synthesis using a commercially available nitroxide-mediated radical polymerization (NMP) initiator

Micro review of reversible addition/fragmentation chain transfer (RAFT) polymerization.

Protocols

We present an article about RAFT, or Reversible Addition/Fragmentation Chain Transfer, which is a form of living radical polymerization.

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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