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Quality Level
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
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
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Tin derivatives for synthesis: the preparation of macrocyclic lactones.
Journal of the Chemical Society. Chemical Communications, 4, 176-177 (1980)
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-
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
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