2,6-Dichloroquinone-4-chloroimide
AR,98.0%
Reagent
Code: #111571
Alias
2,6-Dichloroquinone Chlorimide; 2,6-Dichlorobenzoquinone Chlorimide; 2,6-Dichloro-4-(Chloroimine)-2,5-Cyclohexadiene-1- Ketone
CAS Number
101-38-2
blur_circular Chemical Specifications
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Molecular Information
Weight
210.45 g/mol
Formula
C₆H₂Cl₃NO
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Registry Numbers
EC Number
202-937-2
MDL Number
MFCD00001611
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Physical Properties
Melting Point
65-67 °C(lit.)
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Storage & Handling
Storage
2~8℃
description Product Description
2,6-Dichloroquinone-4-chloroimide is primarily used as a reagent in analytical chemistry for the detection and determination of phenolic compounds. It reacts with phenols to form colored products, which can be measured spectrophotometrically, making it valuable in qualitative and quantitative analysis. This chemical is particularly useful in environmental testing to identify phenolic pollutants in water and soil samples. Additionally, it is employed in pharmaceutical analysis to detect phenolic components in drug formulations. Its specificity and sensitivity to phenols make it a crucial tool in various chemical and biochemical research applications.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Carbon | 32.4-36 |
| Melting Point | 64-67 |
| Nitrogen | 6.3-7.3 |
| Purity (HPLC) | 95-100 |
| Purity (Iodometric Titration) | 95-100 |
| Appearance | Yellow to orange powder and/or chunks |
| Infrared Spectrometry | Conforms To Structure |
| Solubility | Colorless or yellow, clear (50 mg/mL, ethanol) |
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2,6-Dichloroquinone-4-chloroimide
2,6-Dichloroquinone-4-chloroimide is primarily used as a reagent in analytical chemistry for the detection and determination of phenolic compounds. It reacts with phenols to form colored products, which can be measured spectrophotometrically, making it valuable in qualitative and quantitative analysis. This chemical is particularly useful in environmental testing to identify phenolic pollutants in water and soil samples. Additionally, it is employed in pharmaceutical analysis to detect phenolic components in drug formulations. Its specificity and sensitivity to phenols make it a crucial tool in various chemical and biochemical research applications.
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