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2-hydroxybenzene 2,6-Dibromophenol, 1,3-Dibromo-2-hydroxybenzene 3,4-Dibromophenol, 1,2-Dibromo-4-hydroxybenzene 3,5-Dibromophenol, 1,3-Dibromo-5-hydroxybenzene Structural formula: CAS Number: 57383-80-9: 615-58-7: 28165-52-8: 608-33-3: 615-56-5: 626-41-5 PubChem: CID 34264 from PubChem: CID 12005 from PubChem: CID 34177 from PubChem: CID 11847 ...
Chemical structure of 2-bromophenol. A bromophenol is an organic compound consisting of hydroxyl groups and bromine atoms bonded to a benzene ring. They may be viewed as hydroxyl derivatives of bromobenzene, or as brominated derivatives of phenol.
2-Bromophenol: 3-Bromophenol: 4-Bromophenol: Other names o-Bromophenol: m-Bromophenol: p-Bromophenol Chemical structure: CAS number: 95-56-7: 591-20-8: 106-41-2 PubChem ID CID 7244 from PubChem: CID 11563 from PubChem: CID 7808 from PubChem: Chemical formula: C 6 H 5 BrO Molar mass: 173.02 g/mol 1: Physical state: liquid solid Melting point: 3 ...
The odour is caused by 2,6-dibromophenol, a phenol [8] also reported from crustaceans, where it is the cause of a similar odour. [9] [10] Balanglossus gigas also has accumulation of iodine throughout its body, something reported from no other acorn worm or protochordate.
A study was published by the European Food Safety Authority (EFSA) in December 2011 on the exposure of TBBPA and its derivatives in food. The study, which examined at 344 food samples from the fish and other seafood food group, concluded that “current dietary exposure to TBBPA in the European Union does not raise a health concern.”
2,4,6-Tribromophenol (TBP) is a brominated derivative of phenol. It is used as a fungicide, as a wood preservative, and an intermediate in the preparation of flame ...
At room temperature, 2,4-dibromophenol is a solid with needle-like crystals. It melts at 38 °C (100.4 °F) and boils at 238.5 °C (461.3 °F). it has a molecular weight of 251.905 g/mol. It is soluble in water, ethanol, ether and benzene and slightly soluble in carbon tetrachloride. [1]
2,6-Dibromoquinonechlorimide is used in a buffer solution around pH 9.4. It is very sensitive and can detect down to 0.05 parts per million of phenols. The mechanism is the chlorimide group (=NCl) reaction with the phenol to produce an indophenol , with two rings joined via an =N- link.