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723274

4-Cyano-4-[(dodecylsulfanylthiocarbonyl)sulfanyl]pentanoic acid

97% (HPLC)

Synonym(s):

4-Cyano-4-(((dodecylthio)carbonothioyl)thio)pentanoic acid

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About This Item

Empirical Formula (Hill Notation):
C19H33NO2S3
CAS Number:
870196-80-8
Molecular Weight:
403.67
NACRES:
NA.23
PubChem Substance ID:
329763992
UNSPSC Code:
12352100
MDL number:
MFCD11040288
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Quality Level

100

assay

97% (HPLC)

form

solid

mp

64-68 °C

storage temp.

−20°C

SMILES string

CCCCCCCCCCCCSC(=S)SC(C)(CCC(O)=O)C#N

InChI

1S/C19H33NO2S3/c1-3-4-5-6-7-8-9-10-11-12-15-24-18(23)25-19(2,16-20)14-13-17(21)22/h3-15H2,1-2H3,(H,21,22)

InChI key

RNTXYZIABJIFKQ-UHFFFAOYSA-N

General description

Need help choosing the correct RAFT Agent? Please consult the RAFT Agent to Monomer compatibility table.

Application

Reversible Addition Fragmentation Chain Transfer (RAFT) Polymerization

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Deleterious substance

pdsc

723274-5G:4.548173301242E12 + 723274-1G:4.548173301235E12

jan

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Certificates of Analysis (COA)

Lot/Batch Number
MKCX0867
MKCV0818
MKCW4637
MKCW4638
MKCW4639

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Protocols

ATRPによる重合

ウォーリック大学のProf. Dave Haddletonの研究グループによって実証された、ATRPによる重合。

RAFT剤を用いた典型的な重合反応例

RAFT（可逆的付加-開裂連鎖移動）重合によるPMMAおよびPVAcの典型的な重合手順をご紹介します。

Articles

Protein- and Peptide- Polymer Conjugates by RAFT Polymerization

The modification of biomacromolecules, such as peptides and proteins, through the attachment of synthetic polymers has led to a new family of highly advanced biomaterials with enhanced properties.

RAFT Polymerization

RAFT polymerization offers living characteristics to radical polymerization, contributing versatility to reversible deactivation radical polymerization methods.

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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