10081-39-7

10081-39-7 - Names and Identifiers

Name	2,6-diphenyl-4-(2,4,6-triphenyl-1-pyri-dinio)phenolate
Synonyms	REICHARDT'S DYE 4-(2,4,6-Triphenylpyridinio)-2,6-diphenylphenolate 2,6-DIPHENYL-4-(2,4,6-TRIPHENYLPYRIDINIO)PHENOLATE 2,6-DIPHENYL-4-(2,4,6-TRIPHENYL-1-PYRIDINIO)PHENOLATE 2,6-diphenyl-4-(2,4,6-triphenyl-1-pyri-dinio)phenolate 2,6-Diphenyl-4-(2,4,6-triphenylpyridinio)benzene-1-olate 1-(4-Oxylato-3,5-diphenylphenyl)-2,4,6-triphenylpyridinium 2,6-Diphenyl-4-(2,4,6-triphenyl-1-pyridinio)phenolate, 2,6-Diphenyl-4-(2,4,6-triphenylpyridinio)phenolate
CAS	10081-39-7
InChI	InChI=1/C41H29NO/c43-41-37(31-18-8-2-9-19-31)28-36(29-38(41)32-20-10-3-11-21-32)42-39(33-22-12-4-13-23-33)26-35(30-16-6-1-7-17-30)27-40(42)34-24-14-5-15-25-34/h1-29H

10081-39-7 - Physico-chemical Properties

Molecular Formula	C41H29NO
Molar Mass	551.68
Melting Point	271-275°C(lit.)
Solubility	Chloroform (Slightly), Ethyl Acetate (Slightly, Sonicated)
Appearance	Solid
Color	Dark Green to Very Dark Grey
BRN	1444580
Storage Condition	Hygroscopic, -20°C Freezer, Under inert atmosphere
Stability	Stable. Incompatible with acids and strong oxidizing agents.

10081-39-7 - Risk and Safety

Safety Description	S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes.
WGK Germany	3

10081-39-7 - Introduction

2,6-diphenyl-4-(2,4, 6-triphenyl-1-pyridinium) phenolic acid, also known as DPPH(2,6-diphenyl-4-(2,4,6-triphenyl-1-pyridinyl)phenol). The following is a description of its nature, use, formulation and safety information:

Nature:
-Appearance: DPPH is a dark purple crystalline solid.
-Solubility: It is soluble in organic solvents (such as ethanol, dimethylbenzene, dichloromethane), but insoluble in water.
-Oxidative: DPPH is a highly stable free radical that can be reduced by oxidants to colorless products.
-Stability: It is relatively stable to light and heat.

Use:
-Chemical analysis: DPPH can be used as a redox indicator to determine the reduction properties of substances.
-Antioxidant: DPPH is a commonly used natural antioxidant that can be used to detect and evaluate antioxidant properties in foods, drugs and cosmetics.
-Spectroscopy: DPPH can also be used in infrared spectroscopy and fluorescence spectroscopy.

Preparation Method:
The preparation method of DPPH is more complicated and usually needs to be synthesized by chemical reaction. One common method of preparation is the reaction of 2,6-diphenyl -4-cresol with 2,4, 6-triphenylpyridine to give 2,6-diphenyl -4-(2,4, 6-triphenyl-1-pyridinium) benzolic acid.

Safety Information:
- DPPH is relatively safe for human health under general conditions of use.
-It is a non-flammable solid, but contact with combustibles and high temperatures should be avoided.
-During operation, you should wear appropriate personal protective equipment, such as laboratory gloves and glasses, to avoid contact with skin and eyes.
-When performing large-scale synthesis or experimental operations, it is recommended to perform it in a well-ventilated laboratory, and take additional safety measures as needed.

Last Update：2024-04-09 15:17:50