Molecular Formula | C7H3Br3O3 |
Molar Mass | 374.81 |
Density | 2.3705 (rough estimate) |
Melting Point | 145-148 °C (lit.) |
Boling Point | 121°C (rough estimate) |
Flash Point | 168.7°C |
Water Solubility | insoluble |
Vapor Presure | 1.16E-05mmHg at 25°C |
Appearance | Solid |
Color | White |
BRN | 2844497 |
pKa | 1.15±0.10(Predicted) |
Storage Condition | Keep in dark place,Inert atmosphere,Room temperature |
Sensitive | Sensitive to light |
Refractive Index | 1.5438 (estimate) |
MDL | MFCD00055557 |
Use | Ultrapure biochemical reaction chromogen. Good water solubility, high sensitivity and stability |
Risk Codes | R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. R36/37/38 - Irritating to eyes, respiratory system and skin. R20/22 - Harmful by inhalation and if swallowed. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S37/39 - Wear suitable gloves and eye/face protection |
WGK Germany | 3 |
HS Code | 29182900 |
Hazard Class | IRRITANT |
Biological activity | TBHBA (2,4,6-Tribromo-3-hydroxybenzoic acid) is a highly stable dye formed by oxidative coupling reaction with 4-aminoantipyrine (4-AA) or 3-methylbenzothiazolone hydrazone (MBTH) in the presence of hydrogen peroxide and peroxidase. |
Use | Used as biochemical reagent Ultrapure biochemical reaction chromogen. With good water solubility, high sensitivity and strong stability enzyme colorimetric determination, "TBHBA" uric acid is oxidized by uricase in allantoin, and the produced hydrogen peroxide reacts with 4-aminoantipyrine and 2,4, 6-tribromo-3-hydroxybenzoic acid to form Chinonimine. |