5-BROMO-6-CHLORO-3-INDOLYL PHOSPHATE P-TOLUIDINE SALT
5-Bromo-6-chloro-3-indolyl phosphate p-toluidine salt
CAS: 6769-80-8
Molecular Formula: C15H15BrClN2O4P
5-BROMO-6-CHLORO-3-INDOLYL PHOSPHATE P-TOLUIDINE SALT - Names and Identifiers
| Name | 5-Bromo-6-chloro-3-indolyl phosphate p-toluidine salt |
| Synonyms | MAGENTA PHOSPHATE Magenta(R) phosphate MAGENTA(TM)-PHOS P-TOL BCIP RED P-TOLUIDINE SALT MAGENTA(TM)-PHOSPHATE P-TOLUIDINE SALT 5-BROMO-6-CHLORO-3-INDOLYL PHOSPHATEP-TO LUIDINE 5-Bromo-6-chloro-3-indolyl phosphate p-toluidine salt 5-BROMO-6-CHLORO-3-INDOLYL PHOSPHATE P-TOLUIDINE SALT 5-BROMO-6-CHLORO-3-INDOXYL PHOSPHATE, P-TOLUIDINE SALT |
| CAS | 6769-80-8 |
| EINECS | 1533716-785-6 |
| InChI | InChI:1S/C8H6BrClNO4P.C7H9N/c9-5-1-4-7(2-6(5)10)11-3-8(4)15-16(12,13)14;1-6-2-4-7(8)5-3-6/h1-3,11H,(H2,12,13,14);2-5H,8H2,1H3 |
5-BROMO-6-CHLORO-3-INDOLYL PHOSPHATE P-TOLUIDINE SALT - Physico-chemical Properties
| Molecular Formula | C15H15BrClN2O4P |
| Molar Mass | 433.62 |
| Melting Point | 198-200℃ |
| Boling Point | 580.2°C at 760 mmHg |
| Flash Point | 304.7°C |
| Vapor Presure | 2.65E-14mmHg at 25°C |
| Storage Condition | Inert atmosphere,Store in freezer, under -20°C |
5-BROMO-6-CHLORO-3-INDOLYL PHOSPHATE P-TOLUIDINE SALT - Risk and Safety
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| FLUKA BRAND F CODES | 10 |
| HS Code | 29339900 |
5-BROMO-6-CHLORO-3-INDOLYL PHOSPHATE P-TOLUIDINE SALT - Introduction
5-Bromo-6-choro-3-indolyl phosphate p-toluidine salt is an organic compound with the chemical formula C16H16BrClN2O4P. It is a colorless crystalline powder with a blue color when dissolved in an organic solvent such as DMF (N,N-dimethylformamide) or DMSO (dimethyl sulfoxide).
5-Bromo-6-chloroo-3-indolyl phosphate p-toluidine salt is often used as a substrate in biochemical research, especially as a substrate for alkaline phosphatase. It can be combined with alkaline phosphatase to produce a labeled color reaction, which is used in the detection of phosphatase activity, enzyme kinetics and cell signaling.
The method for preparing 5-Bromo-6-chloro-3-indolyl phosphate p-toluidine salt is generally obtained by the reaction of synthesizing indole group and phosphoric acid ester, and then forming hydrochloride with toluidine. Specific synthetic procedures and methods may vary depending on laboratory conditions.
For safety information, 5-Bromo-6-choro-3-indolyl phosphate p-toluidine salt should be considered hazardous to people and the environment. Observe relevant safety operation regulations and protective measures during use and handling. It is recommended to operate in a specialized chemical laboratory environment and prevent contact with skin, eyes and inhalation. If the skin or eyes are exposed, rinse immediately with plenty of water and seek medical attention.
5-Bromo-6-chloroo-3-indolyl phosphate p-toluidine salt is often used as a substrate in biochemical research, especially as a substrate for alkaline phosphatase. It can be combined with alkaline phosphatase to produce a labeled color reaction, which is used in the detection of phosphatase activity, enzyme kinetics and cell signaling.
The method for preparing 5-Bromo-6-chloro-3-indolyl phosphate p-toluidine salt is generally obtained by the reaction of synthesizing indole group and phosphoric acid ester, and then forming hydrochloride with toluidine. Specific synthetic procedures and methods may vary depending on laboratory conditions.
For safety information, 5-Bromo-6-choro-3-indolyl phosphate p-toluidine salt should be considered hazardous to people and the environment. Observe relevant safety operation regulations and protective measures during use and handling. It is recommended to operate in a specialized chemical laboratory environment and prevent contact with skin, eyes and inhalation. If the skin or eyes are exposed, rinse immediately with plenty of water and seek medical attention.
Last Update：2024-04-10 22:29:15
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