Skip to Content
Merck
All Photos(1)

Documents

251313

Sigma-Aldrich

Pimeloyl chloride

98%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
ClCO(CH2)5COCl
CAS Number:
142-79-0
Molecular Weight:
197.06
EC Number:
205-561-7
MDL number:
MFCD00000762
UNSPSC Code:
12352100
PubChem Substance ID:
24855125
NACRES:
NA.22

Assay

98%

refractive index

n20/D 1.469 (lit.)

bp

113 °C/5 mmHg (lit.)

density

1.205 g/mL at 25 °C (lit.)

SMILES string

ClC(=O)CCCCCC(Cl)=O

InChI

1S/C7H10Cl2O2/c8-6(10)4-2-1-3-5-7(9)11/h1-5H2

InChI key

LVIMBOHJGMDKEJ-UHFFFAOYSA-N

Application

Pimeloyl chloride has been used in preparation of:
  • bis-acylureas, by the coupling reaction with ureas
  • triacetyl-15-pimelate-nivalenol, required for production of antibody against nivalenol tetraacetate
  • macrocyclic tetralactones, via condensation with stannoxane

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H314,H335

Hazard Classifications

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

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

Tin derivatives for synthesis: the preparation of macrocyclic lactones.
Shanzer A and Mayer-Shochet N.
Journal of the Chemical Society. Chemical Communications, 4, 176-177 (1980)
Jong-Uk Kim et al.
Journal of colloid and interface science, 359(2), 428-435 (2011-05-04)
We present the synthesis and morphology study of thirteen bis-acylurea molecules with various functional end groups. The bis-acylureas have two acylurea groups, -NH-CO-NH-CO-, divided by a pentamethylene spacer, -(CH(2))(5)-, and two symmetric functional end groups, such as, aliphatic, benzyl, mono-
C R Wang et al.
Applied and environmental microbiology, 57(4), 1026-1030 (1991-04-01)
Antibody against nivalenol tetraacetate (tetra-Ac-NIV) was prepared by immunization of rabbits with triacetyl-15-pimelate-NIV conjugated to bovine serum albumin. By using tritiated tetra-Ac-NIV as the test ligand, antibody titers were demonstrated as early as 4 weeks after immunization. Useful antibody for

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