| Identification | More | [Name]
2,4-Dibromophenol | [CAS]
615-58-7 | [Synonyms]
2,4-DIBROMOPHENOL
AKOS BBB/366
2,4-dibromo-pheno
Emery 9331
FR-612
Phenol, 2,4-dibromo-
phenol,2,4-dibromo
2,4-DIBROMOPHENOL, 1000MG,NEAT
2,4-Dibromophenol, tech.
2,4-Dibromophenol,95%
2,4-BROMOPHENOL | [EINECS(EC#)]
210-436-5 | [Molecular Formula]
C6H4Br2O | [MDL Number]
MFCD00002149 | [Molecular Weight]
251.9 | [MOL File]
615-58-7.mol |
| Safety Data | Back Directory | [Hazard Codes ]
T,Xi,Xn | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin .
R25:Toxic if swallowed.
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . | [Safety Statements ]
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S37/39:Wear suitable gloves and eye/face protection .
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 .
S36:Wear suitable protective clothing . | [RIDADR ]
2811 | [WGK Germany ]
3 | [RTECS ]
SK8010000 | [Hazard Note ]
Irritant | [TSCA ]
Yes | [HazardClass ]
6.1 | [PackingGroup ]
II | [HS Code ]
29081990 | [Hazardous Substances Data]
615-58-7(Hazardous Substances Data) |
| Hazard Information | Back Directory | [Chemical Properties]
white crystalline powder | [Definition]
ChEBI: 2,4-dibromophenol is a bromophenol that is phenol in which the hydrogens at positions 2 and 4 have been replaced by bromines. It has a role as a marine metabolite. It is a bromophenol, a dibromobenzene and a brominated flame retardant. | [Synthesis Reference(s)]
Tetrahedron, 45, p. 7869, 1989 DOI: 10.1016/S0040-4020(01)85800-2 | [General Description]
The electrochemical hydrodehalogenation of 2,4-dibromophenol has been studied by electrochemical reduction in H-cells and solid polymer electrolyte cells using catalyzed cathodes. 2,4-Dibromophenol inhibits the microbial activity in marine sediments. | [Purification Methods]
Crystallise the phenol from CHCl3 at -40o, or distil it in a vacuum. [Beilstein 6 H 202, 6 I 106, 6 II 188, 6 III 753, 6 IV 1061.] |
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