| Identification | More | [Name]
Cycloheptatriene | [CAS]
544-25-2 | [Synonyms]
1，3，5-Cycioheptatriene
1,3,5-CYCLOHEPTATRIENE
CHT
CYCLOHEPTATRIENE
TROPILIDENE
Cyclohepta-1,3,5-triene
Cycloheptatrien
tropiliden
Tropilidin
Cycloheptatrienetech
Tropylidene
CYCLOHEPTATRIENE, STANDARD FOR GC
Cycloheptatriene,tech.90%
1,3,5-Cycloheptariene
Cyclohepta-2,4,6-triene | [EINECS(EC#)]
208-866-3 | [Molecular Formula]
C7H8 | [MDL Number]
MFCD00004146 | [Molecular Weight]
92.14 | [MOL File]
544-25-2.mol |
| Safety Data | Back Directory | [Hazard Codes ]
F,T | [Risk Statements ]
R11:Highly Flammable.
R25:Toxic if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin .
R65:Harmful: May cause lung damage if swallowed. | [Safety Statements ]
S16:Keep away from sources of ignition-No smoking .
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 .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S62:If swallowed, do not induce vomiting: seek medical advice immediately and show this container or label . | [RIDADR ]
UN 2603 3/PG 2
| [WGK Germany ]
3
| [RTECS ]
GU3675000
| [F ]
10-23 | [HazardClass ]
3 | [PackingGroup ]
II | [HS Code ]
29021990 | [Safety Profile]
Poison by ingestion and
skin contact. Mutation data reported. A very
dangerous fire hazard when exposed to heat,
flame, or oxidzers. Potentially violent
reaction with nitrogen monoxide. Whenheated to decomposition it emits acrid
smoke and fumes. |
| Hazard Information | Back Directory | [General Description]
A colorless liquid. Insoluble in water and less dense than water. Flash point 35°F. Vapors heavier than air. Inhalation of high concentrations may have a narcotic effect. Used to make other chemicals. | [Reactivity Profile]
CYCLOHEPTATRIENE(544-25-2) may react vigorously with strong oxidizing agents. May react exothermically with reducing agents to release hydrogen gas. In the presence of various catalysts (such as acids) or initiators, may undergo exothermic addition polymerization reactions. | [Air & Water Reactions]
Highly flammable. Insoluble in water. | [Health Hazard]
TOXIC; may be fatal if inhaled, ingested or absorbed through skin. Inhalation or contact with some of these materials will irritate or burn skin and eyes. Fire will produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution. | [Fire Hazard]
HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion and poison hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water. | [Chemical Properties]
Cycloheptatriene is a clear yellow to brownish liquid. Insoluble in water and less dense than water. Vapors heavier than air. Inhalation of high concentrations may have a narcotic effect. It is a ligand in organometallic chemistry and as a building block in organic synthesis. Cycloheptatriene is not aromatic, as reflected by the nonplanarity of the methylene bridge with respect to the other atoms. | [Uses]
1,3,5-Cycloheptatriene functions as a ligand in organometallic chemistry and also as a building block in organic synthetic processes. 1,3,5-Cycloheptatriene is applied in cycloheptatrienyl transition zirconium complexes formation and in other organic complex formation processes. | [Definition]
ChEBI: A cycloheptatriene with unsaturation at positions 1, 3 and 5. | [Synthesis Reference(s)]
Journal of the American Chemical Society, 81, p. 5009, 1959 DOI: 10.1021/ja01527a075
Tetrahedron, 21, p. 1673, 1965 DOI: 10.1016/S0040-4020(01)98637-5 | [Purification Methods]
Wash the triene with alkali, then fractionally distil it. Store it under N2 or Ar as it resinifies in air. [Dryden J Am Chem Soc 76 2814 1954, Kohler et al. J Am Chem Soc 61 1057 1939, Beilstein 5 IV 280.] |
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