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| | 1,6-Dibromohexane Basic information |
| Product Name: | 1,6-Dibromohexane | | Synonyms: | 1,6-Dibromhexan;1,6-Dibromohexan;1,6-dibromo-hexan;1,6-Dibromohexane,98%;1,6-DibroMohexane, 98% 100ML;1,6-DibroMohexane, 98% 500ML;Hexamethylene Bromide
Hexamethylene Dibromide;1,6-DIBROMOHEXANE FOR SYNTHESIS | | CAS: | 629-03-8 | | MF: | C6H12Br2 | | MW: | 243.97 | | EINECS: | 211-067-2 | | Product Categories: | Industrial/Fine Chemicals;DIBROMOALKANE;Bromine Compounds;alpha,omega-Bifunctional Alkanes;alpha,omega-Dibromoalkanes;Monofunctional & alpha,omega-Bifunctional Alkanes;bc0001 | | Mol File: | 629-03-8.mol |  |
| | 1,6-Dibromohexane Chemical Properties |
| Melting point | -2-2.5 °C (lit.) | | Boiling point | 243 °C (lit.) | | density | 1.586 g/mL at 25 °C (lit.) | | vapor pressure | <1 hPa (20 °C) | | refractive index | n20/D 1.507(lit.) | | Fp | 110 °C | | storage temp. | Store below +30°C. | | solubility | soluble in Chloroform, Ethyl Acetate | | form | Liquid | | color | colorless to brownish-yellow | | Water Solubility | insoluble | | BRN | 1236322 | | Stability: | Stable. Incompatible with strong oxidizing agents. | | InChIKey | SGRHVVLXEBNBDV-UHFFFAOYSA-N | | CAS DataBase Reference | 629-03-8(CAS DataBase Reference) | | NIST Chemistry Reference | Hexane, 1,6-dibromo-(629-03-8) | | EPA Substance Registry System | Hexane, 1,6-dibromo- (629-03-8) |
| Hazard Codes | T,N,C | | Risk Statements | 25-51/53-43 | | Safety Statements | 36-45-61-36/37 | | RIDADR | UN 2810 6.1/PG 3 | | WGK Germany | 3 | | RTECS | MO1515000 | | TSCA | Yes | | HazardClass | 9 | | PackingGroup | III | | HS Code | 29033036 | | Toxicity | LD50 orally in Rabbit: 1800 mg/kg LD50 dermal Rabbit > 2000 mg/kg |
| | 1,6-Dibromohexane Usage And Synthesis |
| Chemical Properties | colourless or pale yellow liquid. soluble in ethanol, ether, benzene and chloroform, insoluble in water. It is used in the synthesis of the hypotensive drug hexamethonium bromide. | | Uses | 1,6-Dibromohexane is used as a reagent in the synthesis of novel benzo[b]xanthone derivatives which have a potential antitumor activity. It is also used as a cross-linker for the cross-linking of glycuronans. | | Uses | 1,6-Dibromohexane is generally used to introduce C6 spacer in the molecular architecture. Some of the examples are:
Synthesis of solvent processable and conductive polyfluorene ionomers for alkaline fuel cell applications.
Synthesis of cross-linkable regioregular poly(3-(5-hexenyl)thiophene) (P3HNT) for stabilizing the film morphology in polymer photovoltaic cells.
Synthesis of pyrrolo-tetrathiafulvalene molecular bridge (6PTTF6) to study redox switching behavior of single molecules.
Synthesis of water-soluble thermoresponsive polylactides. | | Preparation | 1,6-Dibromohexane is synthesized from hexanediol by bromination. |
| | 1,6-Dibromohexane Preparation Products And Raw materials |
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