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Merck
CN

236365

Sebacoyl chloride

99%

Synonym(s):

Sebacyl chloride

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About This Item

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

Key Documents

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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

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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

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
MKCX3086
MKCT5504
MKCN5598
MKCM7520
MKCJ5012

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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)
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)
P L Madan et al.
Pharmaceutical research, 6(8), 714-718 (1989-08-01)
The effect of selected variables on the release characteristics of theophylline microcapsules prepared with 1,6-hexamethylene diamine and sebacoyl chloride via interfacial polycondensation has been investigated. The nature of the microcapsules and the release characteristics of theophylline from the microcapsules were
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
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