
2,6-Dichloroindophenol Sodium Salt, also known as 2,6-Dichlorophenolindophenol Sodium Salt Dihydrate (DCPIP, DCIP, or DPIP), is a synthetic indophenol dye widely used as a redox indicator and analytical reagent. It is best known for the determination of vitamin C (ascorbic acid), where it changes from its blue oxidized form to a colorless reduced form during the reaction. In its oxidized state, it shows a maximum absorption of about 600 nm, making it valuable for spectrophotometric and oxidation-reduction analyses.

CAS No.: 620-45-1
Synonyms: 2,6-Dichlorobenzenone-indophenolsodium salt, Tillman’s reagent, 2,6-Dichlorophenol Indophenol Sodium SaltÂ
| Physical Properties | |
| Chemical formula | C12H6Cl2NNaO2 |
| IUPAC Name | sodium 4-[(3,5-dichloro-4-oxocyclohexa-2,5-dien-1-ylidene)amino]phenolate |
| Molecular weight | 290.07 g/mol |
| Solubility | Soluble in water |
| Appearance | Dark green to Dark purple powder |
| Storage | Store at room temperature |
| Chemical Properties | |
| Color | Dark Green |
| Physical State at 20 °C | Solid |
| Melting Point | >300 °C |
| Odor | Odorless |
| Pictograms : | ![]() |
| Hazard Statements : | H315: Causes skin irritation. H319: Causes serious eye irritation. H335: May cause respiratory irritation. |
| Precautionary statements : | P261: Avoid breathing dust/fume/gas/mist/vapours/spray. P304+P340: IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing. P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.   |
2,6-Dichloroindophenol Sodium Salt, also known as 2,6-Dichlorophenolindophenol Sodium Salt Dihydrate (DCPIP, DCIP, or DPIP), is a synthetic indophenol dye widely used as a redox indicator and analytical reagent. It is best known for the determination of vitamin C (ascorbic acid), where it changes from its blue oxidized form to a colorless reduced form during the reaction. In its oxidized state, it shows a maximum absorption of about 600 nm, making it valuable for spectrophotometric and oxidation-reduction analyses.

CAS No.: 620-45-1
Synonyms: 2,6-Dichlorobenzenone-indophenolsodium salt, Tillman’s reagent, 2,6-Dichlorophenol Indophenol Sodium SaltÂ
| Physical Properties | |
| Chemical formula | C12H6Cl2NNaO2 |
| IUPAC Name | sodium 4-[(3,5-dichloro-4-oxocyclohexa-2,5-dien-1-ylidene)amino]phenolate |
| Molecular weight | 290.07 g/mol |
| Solubility | Soluble in water |
| Appearance | Dark green to Dark purple powder |
| Storage | Store at room temperature |
| Chemical Properties | |
| Color | Dark Green |
| Physical State at 20 °C | Solid |
| Melting Point | >300 °C |
| Odor | Odorless |
| Pictograms : | ![]() |
| Hazard Statements : | H315: Causes skin irritation. H319: Causes serious eye irritation. H335: May cause respiratory irritation. |
| Precautionary statements : | P261: Avoid breathing dust/fume/gas/mist/vapours/spray. P304+P340: IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing. P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.   |
2,6-Dichloroindophenol Sodium Salt is mainly used for vitamin C determination, redox reactions, photosynthesis studies, spectrophotometric analysis, electron transfer experiments, and electrophoresis staining.
2,6-Dichloroindophenol Sodium Salt (DCPIP) functions as a redox dye. In its oxidized state it is blue, and when it accepts electrons during a reduction reaction, it becomes colorless.
2,6-Dichloroindophenol Sodium Salt should be handled using appropriate laboratory safety practices such as wearing suitable personal protective equipment, avoiding inhalation or ingestion, and follow the safety instructions provided in the product Safety Data Information.
2,6-Dichloroindophenol Sodium Salt acts as an artificial electron acceptor (Hill reagent), replacing NADP+ to observe electron transport during photosynthesis.
The Dichloroindophenol test is a colorimetric method used to establish vitamin C concentration by measuring the reduction of DCPIP from blue to colorless.