Name | DIBROMOISOCYANURIC ACID |
Synonyms | DIBROMOISOCYANURIC ACID 1,3-DibroMoisocyanuricacid 1,3-Dibromo-1,3,5-triazine-2,4,6-trione 1,3-Dibromo-1,3,5-triazinane-2,4,6-trione 1,3-dibromo-1,3,5-triazinane-2,4,6-trione 1,3-Dibromo-1,3,5-triazine-2,4,6-trioneDBI Dibromoisocyanuric acid, 1,3-Dibromo-1,3,5-triazine-2,4,6-trione Dibromoisocyanuric acid, 1,3-Dibromo-2,4,6-trioxo-1,3,5-triazinane |
CAS | 15114-43-9 |
InChI | InChI=1/C3HBr2N3O3/c4-7-1(9)6-2(10)8(5)3(7)11/h(H,6,9,10) |
InChIKey | HHBCEKAWSILOOP-UHFFFAOYSA-N |
Molecular Formula | C3HBr2N3O3 |
Molar Mass | 286.87 |
Density | 2.789±0.06 g/cm3(Predicted) |
Melting Point | 309 °C |
Solubility | DMSO, Methanol |
Appearance | Solid |
Color | Off-White to Pale Yellow |
pKa | 3.23±0.20(Predicted) |
Storage Condition | 2-8°C |
Refractive Index | 1.712 |
Risk Codes | R8 - Contact with combustible material may cause fire R22 - Harmful if swallowed R31 - Contact with acids liberates toxic gas R34 - Causes burns R50/53 - Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. |
Safety Description | S8 - Keep container dry. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S41 - In case of fire and / or explosion do not breathe fumes. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) S60 - This material and its container must be disposed of as hazardous waste. S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. |
UN IDs | UN 3085 8(5.1) / PGII |
WGK Germany | 3 |
HS Code | 29336990 |
Hazard Class | 5.1/8 |
Packing Group | II |
Use | 1, 3-dibromo-1, 3, 5-triazine-2, 4, 6-trione is a mild and efficient bromination reagent. Compared with N-bromosuccinimide (NBS), which is commonly used in organic synthesis, it also has better bromination ability. 1, 3-dibromo-1, 3, 5-triazine-2, 4, 6-trione is a mild and efficient brominating reagent. Compared with N-bromosuccinimide (NBS), which is commonly used in organic synthesis, it also has better bromination ability. Under the condition of adding DBI to concentrated sulfuric acid and reacting at room temperature of 20 ° C. For 5min, nitrobenzene was converted into 3-bromo derivative, and the yield was 88%. In the same experiment, NBS was added to 50% sulfuric acid and reacted at 85 ° C. For 3H, and the yield was only 50%. Therefore, DBI has been widely used as a highly efficient bromination reagent. |