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| 2,6-DIISOPROPYLNAPHTHALENE Basic information |
Product Name: | 2,6-DIISOPROPYLNAPHTHALENE | Synonyms: | 2,6-bis(1-methylethyl)-naphthalen;Naphthalene, 2,6-bis(1-methylethyl)-;Naphthalene, 2,6-diisopropyl-;2,6-DIISOPROPYLNAPHTHALENE;2,6-BIS(1-METHYLETHYL)-NAPHTHALENE;2,6-DIISOPRYLNAPHTHALENE;2,6-DIISOPROPYL NAHPTHALENE TECHNICAL;2,6-diisopropyl naphtalene | CAS: | 24157-81-1 | MF: | C16H20 | MW: | 212.33 | EINECS: | 246-045-1 | Product Categories: | Color Former & Related Compounds;Functional Materials;Sensitizer | Mol File: | 24157-81-1.mol | |
| 2,6-DIISOPROPYLNAPHTHALENE Chemical Properties |
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) |
Hazard Codes | Xn,N | Risk Statements | 22-50/53 | Safety Statements | 24/25-61-60 | RIDADR | 3077 | TSCA | Yes | HazardClass | 9 | PackingGroup | III | HS Code | 29029090 |
| 2,6-DIISOPROPYLNAPHTHALENE Usage And Synthesis |
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. | General Description | Clear yellowish brown liquid with a faint sweet odor. | Air & Water Reactions | Insoluble in water. | Reactivity Profile | Vigorous reactions, sometimes amounting to explosions, can result from the contact between aromatic hydrocarbons, such as 2,6-DIISOPROPYLNAPHTHALENE, 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]. | 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. | Flammability and Explosibility | Notclassified |
| 2,6-DIISOPROPYLNAPHTHALENE Preparation Products And Raw materials |
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