Dodecahydrotriphenylene
Dodecahydrotriphenylene Basic information
- Product Name:
- Dodecahydrotriphenylene
- Synonyms:
-
- DODECAHYDROTRI-O-PHENYLENE
- DODECAHYDROTRIPHENYLENE
- 1,2,3,4,5,6,7,8,9,10,11,12-Dodecahydrotriphenylene
- 1,2,3,4,4a,4b,5,6,7,8,8a,8b-dodecahydrotriphenylene
- triphenylene,1,2,3,4,5,6,7,8,9,10,11,12-dodecahydro-
- Tritetralin
- Dodecahydrotriphenylene,99%
- 200000.000 KG
- CAS:
- 1610-39-5
- MF:
- C18H24
- MW:
- 240.38
- EINECS:
- 216-550-1
- Product Categories:
-
- Arenes
- Building Blocks
- Miscellaneous
- Organic Building Blocks
- Mol File:
- 1610-39-5.mol
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Dodecahydrotriphenylene Chemical Properties
- Melting point:
- 231-233 °C (lit.)
- Boiling point:
- 318.11°C (rough estimate)
- Density
- 0.9356 (estimate)
- refractive index
- 1.5500 (estimate)
- solubility
- hexane: soluble
- BRN
- 2051002
- CAS DataBase Reference
- 1610-39-5(CAS DataBase Reference)
- NIST Chemistry Reference
- Triphenylene, 1,2,3,4,5,6,7,8,9,10,11,12-dodecahydro-(1610-39-5)
MSDS
- Language:English Provider:Dodecahydrotriphenylene
- Language:English Provider:SigmaAldrich
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Dodecahydrotriphenylene Usage And Synthesis
Chemical Properties
white to yellow-beige fine crystalline powder
Uses
Dodecahydrotriphenylene was used to develop a set of new bacterial bioreporters and assays for detection of long chain alkanes based on the marine bacterium Alcanivorax borkumensis strain SK2.
General Description
Dodecahydrotriphenylene forms metal-carbonyl complexes. It undergoes hydrogenation and rearrangement by action of AlCl3 in inert atmosphere conditions at 20°C (hexane solution) or 70°C (heptane solution). It is formed by trimerization of cyclohexanone. It undergoes oxidation by peroxytrifluoroacetic acid and boron fluoride etherate at 0°C to form cross-conjugated cyclohexadieone.
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