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Sigma-Aldrich

Pimeloyl chloride

98%

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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)

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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
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-
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)

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