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763071

Sigma-Aldrich

3,5-Bis(2-dodecylthiocarbonothioylthio-1-oxopropoxy)benzoic acid

98% (HPLC)

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About This Item

Fórmula empírica (notación de Hill):
C39H62O6S6
Peso molecular:
819.30
MDL number:
MFCD22666443
UNSPSC Code:
12352100
PubChem Substance ID:
329767026
NACRES:
NA.23

assay

98% (HPLC)

form

powder or crystals

mp

60-65 °C

storage temp.

2-8°C

SMILES string

CCCCCCCCCCCCSC(=S)SC(C)C(=O)Oc1cc(OC(=O)C(C)SC(=S)SCCCCCCCCCCCC)cc(c1)C(O)=O

InChI

1S/C39H62O6S6/c1-5-7-9-11-13-15-17-19-21-23-25-48-38(46)50-30(3)36(42)44-33-27-32(35(40)41)28-34(29-33)45-37(43)31(4)51-39(47)49-26-24-22-20-18-16-14-12-10-8-6-2/h27-31H,5-26H2,1-4H3,(H,40,41)

InChI key

GOLRGLNMILBFFI-UHFFFAOYSA-N

General description

Need help choosing the correct RAFT Agent? Please consult the RAFT Agent to Monomer compatibility table.
Reversible addition-fragmentation chain transfer (RAFT) polymerization is used to produce narrow polydispersity polymers of complex architecture. 3,5-Bis(2-dodecylthiocarbonothioylthio-1-oxopropoxy)benzoic acid is a carboxylic acid functionalised trithiocarbonate RAFT agent. It is used to form well-defined block copolymers. They have good control of polymerisation for a wide range of vinyl monomers.

Application

Used in the synthesis of macro-Chain Transfer Agent (CTA) which are used in the RAFT polymerisation of vinylic monomers like styrene, acrylate and acrylamide.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Block copolymers of poly (2-oxazoline) s and poly (meth) acrylates: a crossover between cationic ring-opening polymerization (CROP) and reversible addition-fragmentation chain transfer (RAFT).
Krieg, A., Weber, C., Hoogenboom, R., Becer, C. R., & Schubert, U. S.
ACS Macro Letters, 1(6), 776-779 (2012)
Thiocarbonylthio compounds (SC (Z) SR) in free radical polymerization with reversible addition-fragmentation chain transfer (RAFT polymerization).
Chiefari, J., Mayadunne, R. T., Moad, C. L., Moad, G., Rizzardo, E., Postma, A., & Thang, S. H.
Macromolecules, 36(7), 2273-2283 (2003)
One-step synthesis of block copolymers using a hydroxyl-functionalized trithiocarbonate RAFT agent as a dual initiator for RAFT polymerization and ROP
Kang, H. U., Yu, Y. C., Shin, S. J., & Youk, J. H.
Journal of Polymer Science Part A: Polymer Chemistry, 51(4), 774-779 (2013)
Massimo Benaglia et al.
Journal of the American Chemical Society, 131(20), 6914-6915 (2009-05-01)
The polymerization of most monomers that are polymerizable by radical polymerization can be controlled by the reversible addition-fragmentation chain transfer (RAFT) process. However, it is usually required that the RAFT agent be selected according to the types of monomer being

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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.

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