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364754

Sigma-Aldrich

trans-4-Nitrocinnamoyl chloride

97%

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About This Item

Linear Formula:
O2NC6H4CH=CHCOCl
CAS Number:
Molecular Weight:
211.60
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

powder

mp

150-153 °C (lit.)

SMILES string

[O-][N+](=O)c1ccc(\C=C\C(Cl)=O)cc1

InChI

1S/C9H6ClNO3/c10-9(12)6-3-7-1-4-8(5-2-7)11(13)14/h1-6H/b6-3+

InChI key

RUPXNPWALFDXJD-ZZXKWVIFSA-N

Application

trans-4-Nitrocinnamoyl chloride may be used as derivatization reagent for the analysis of perhexiline and its monohydroxy metabolite in plasma by HPLC. It may be used as derivatization reagent to investigate the in vitro enzyme kinetics and CYP isoform selectivity of perhexiline monohydroxylation using human liver microsomes.

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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N Grgurinovich
Journal of chromatography. B, Biomedical sciences and applications, 696(1), 75-80 (1997-08-15)
A high-performance liquid chromatographic method for the analysis of perhexiline and its monohydroxy metabolite in plasma has been developed. After a simple extraction procedure, the analytes are derivatized over a 30-min period with trans-4-nitrocinnamoyl chloride. The derivatized products are monitored
L B Sørensen et al.
British journal of clinical pharmacology, 55(6), 635-638 (2003-06-20)
The aims of this study were to examine the in vitro enzyme kinetics and CYP isoform selectivity of perhexiline monohydroxylation using human liver microsomes. Conversion of rac-perhexiline to monohydroxyperhexiline by human liver microsomes was assessed using a high-performance liquid chromatography

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