Identification | More | [Name]
2,6-DIISOPROPYLNAPHTHALENE | [CAS]
24157-81-1 | [Synonyms]
2,6-BIS(1-METHYLETHYL)-NAPHTHALENE 2,6-DIISOPROPYLNAPHTHALENE 2,6-bis(1-methylethyl)-naphthalen Naphthalene, 2,6-bis(1-methylethyl)- Naphthalene, 2,6-diisopropyl- 2,6-DIISOPRYLNAPHTHALENE 2,6-DIISOPROPYL NAHPTHALENE TECHNICAL | [EINECS(EC#)]
246-045-1 | [Molecular Formula]
C16H20 | [MDL Number]
MFCD00021648 | [Molecular Weight]
212.33 | [MOL File]
24157-81-1.mol |
Chemical Properties | Back Directory | [Appearance]
beige crystalline platelets | [Melting point ]
67-70 °C | [Boiling point ]
279.3 °C | [density ]
0.9560 (estimate) | [vapor pressure ]
0.08Pa at 25℃ | [refractive index ]
1.5774 (estimate) | [RTECS ]
QJ1536000 | [Fp ]
140 °C
| [solubility ]
Acetonitrile (Slightly), Chloroform (Slightly), Methanol | [form ]
powder to crystal | [color ]
White to Almost white | [Specific Gravity]
0.968 | [Water Solubility ]
1mg/L at 25℃ | [LogP]
6.5 at 25℃ | [CAS DataBase Reference]
24157-81-1(CAS DataBase Reference) | [EPA Substance Registry System]
2,6-Diisopropylnaphthalene (24157-81-1) |
Safety Data | Back Directory | [Hazard Codes ]
Xn,N | [Risk Statements ]
22-50/53 | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [RIDADR ]
3077 | [TSCA ]
Yes | [HazardClass ]
9 | [PackingGroup ]
III | [HS Code ]
29029090 |
Hazard Information | Back Directory | [General Description]
Clear yellowish brown liquid with a faint sweet odor. | [Reactivity Profile]
Vigorous reactions, sometimes amounting to explosions, can result from the contact between aromatic hydrocarbons, such as DIISOPROPYL NAPHTHALENE(24157-81-1), and strong oxidizing agents. They can react exothermically with bases and with diazo compounds. Substitution at the benzene nucleus occurs by halogenation (acid catalyst), nitration, sulfonation, and the Friedel-Crafts reaction. Friedel-Crafts acylation of naphthalene using benzoyl chloride, catalyzed by AlCl3, must be conducted above the melting point of the mixture, or the reaction may be violent [Clar, E. et al., Tetrahedron, 1974, 30, 3296]. | [Air & Water Reactions]
Insoluble in water. | [Health Hazard]
Exposure can cause irritation of eyes, nose and throat. | [Fire Hazard]
Special Hazards of Combustion Products: Irritating vapors and toxic gases, such as carbon dioxide and carbon monoxide, may be formed when involved in fire. | [Chemical Properties]
beige crystalline platelets | [Uses]
2,6-Diisopropylnaphthalene, is a building block used for the synthesis of more complex compounds. 2,6-Diisopropylnaphthalene (2,6-DIPM) is also used in the manufacturing of pesticide products intended to prevent sprouting of stored potatoes. | [Definition]
ChEBI: 2,6-diisopropylnaphthalene is a member of the class of napthalenes that is naphthalene which is substituted by an isopropyl group at positions 2 and 6. It is a plant growth regulator which inhibits the sprouting of potatoes during storage. It has a role as a plant growth retardant and an agrochemical. | [Flammability and Explosibility]
Notclassified |
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