CB-110 - Names and Identifiers
Name | 2,3,3,4,6-Pentabromobiphenyl
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Synonyms | CB-110 PCB 110 BZNO 110 PCB NO 110 2,3,3,4,6-Pentabromobiphenyl 2,3,3',4',6-PENTACHLOROBIPHENYL 2,3,3',4',6-Pentachloro-1,1'-biphenyl 2,3,3',4',6-PENTACB UNLABELED CERTIFIED STANDARD
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CAS | 38380-03-9
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EINECS | 630-502-0 |
CB-110 - Physico-chemical Properties
Molecular Formula | C12H5Cl5
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Molar Mass | 326.43 |
Density | 1.5220 (rough estimate) |
Melting Point | 95.86°C (estimate) |
Boling Point | 412.3°C (rough estimate) |
Water Solubility | 28.82ug/L(20 ºC) |
Storage Condition | Room Temprature |
Refractive Index | 1.6200 (rough estima |
CB-110 - Risk and Safety
Risk Codes | R33 - Danger of cumulative effects
R50/53 - Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.
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Safety Description | S35 - This material and its container must be disposed of in a safe way.
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.
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UN IDs | UN 3432 9/PG 2 |
RTECS | DV8201000 |
CB-110 - Introduction
2,3,3,4,6-Pentabromobiphenyl is an organic compound with the chemical formula C12H5Br5. The following is a detailed description of its nature, use, preparation and safety information:
Nature:
2,3,3,4,6-Pentabromobiphenyl is a solid with yellow crystals and a melting point of about 150-155 degrees Celsius. It is almost insoluble in water at room temperature, but soluble in organic solvents such as ether, dichloromethane, etc. It is stable to air and has high thermal stability.
Use:
2,3,3,4,6-Pentabromobiphenyl is a bromide, which is widely used in electronic components, plastics and foam materials in electronic equipment to improve its flame retardant properties. It can also be used as a flame retardant for coatings, adhesives and polymer additives.
Preparation Method:
The preparation of 2,3,3,4,6-Pentabromobiphenyl can be obtained by reacting brominated biphenyl with hydrogen bromide. The specific preparation method involves organic synthetic chemistry and needs to be carried out under appropriate laboratory conditions.
Safety Information:
Last Update:2024-04-10 22:29:15