Skip to Content
Merck
CN
All Photos(1)

Documents

Safety Information

236365

Sigma-Aldrich

Sebacoyl chloride

99%

Sign Into View Organizational & Contract Pricing
All Photos(1)
Synonym(s):
Sebacyl chloride
Linear Formula:
ClCO(CH2)8COCl
CAS Number:
111-19-3
Molecular Weight:
239.14
Beilstein:
1365665
EC Number:
203-843-4
MDL number:
MFCD00000770
UNSPSC Code:
12162002
PubChem Substance ID:
24854167
NACRES:
NA.23

Quality Level

100

Assay

99%

form

liquid

refractive index

n20/D 1.468 (lit.)

bp

168 °C/12 mmHg (lit.)

mp

−5-−3 °C (lit.)

density

1.121 g/mL at 25 °C (lit.)

SMILES string

ClC(=O)CCCCCCCCC(Cl)=O

InChI

1S/C10H16Cl2O2/c11-9(13)7-5-3-1-2-4-6-8-10(12)14/h1-8H2

InChI key

WMPOZLHMGVKUEJ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Sebacocyl chloride (SC) can be used as a lipophilic monomer for the formation of polyamide microcapsules by an interfacial polycondensation reaction. It can also be utilized in the synthesis of modified chitosan nanoparticle hydrogels with high absorption capacity and high swelling ratio for the removal of metal ions from an aqueous solution. SC can also be used in the preparation of sebacic biscyclocarbonate, which can be used in the synthesis of biobased nonisocyanate polyurethanes.

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H314,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Preparation of robust polyamide microcapsules by interfacial polycondensation of p-phenylenediamine and sebacoyl chloride and plasticization with oleic acid
Rosa N, et al.
Journal of Microencapsulation, 32(4), 349-357 (2015)
Synthesis and in vitro Anti-tumor Activity of Some New Sebacoyl Chloride Based Heterocycles
H El Azab I and AA EN
Current Organic Synthesis, 14(2), 309-320 (2017)
Chitosan nanoparticle hydrogel based sebacoyl moiety with remarkable capability for metal ion removal from aqueous systems
Kandile NG and Mohamed HM
International Journal of Biological Macromolecules, 122(4), 578-586 (2019)
Zhenhua Xu et al.
International journal of pharmaceutics, 426(1-2), 182-192 (2012-01-24)
In this study we describe a novel polymer, mPPS-FA, synthesized as a potential gene transfer vector. To complete mPPS-FA, folic acid was conjugated to a backbone (named mPPS) consisting of a copolymer of methyl PEG-2000, PEI-600, and sebacoyl chloride. (1)H
D Poncelet et al.
Journal of microencapsulation, 11(1), 31-40 (1994-01-01)
A microencapsulation technique is proposed involving the formation of a polyethyleneimine (PEI) membrane crosslinked by an acid dichloride. The membranes were formed at pH 8 in a non-polar solvent, conditions which are better suited for the encapsulation of biocatalysts or
View All Related Papers

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

Contact Technical Service