2,6-DIISOPROPYLNAPHTHALENE
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
- Flash point:
- 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 Information
- 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
Not classified
2,6-DIISOPROPYLNAPHTHALENE Preparation Products And Raw materials
Preparation Products
2,6-DIISOPROPYLNAPHTHALENESupplier
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2,6-DIISOPROPYLNAPHTHALENE(24157-81-1)Related Product Information
- DIISOPROPYLNAPHTHALENE,Diisopropylnaphthalene: (Bis(isopropyl)naphthalene)
- 3,7-DI(TERT-BUTYL)-1,5-DINITRONAPHTHALENE
- TIPS
- Dibunate sodium
- 2,6-Di-tert-butylnaphthalene
- 2,6-DIISOPROPYLNAPHTHALENE
- sodium diisopropylnaphthalenesulphonate
- 2,7-DIISOPROPYLNAPHTHALENE,3,6-diisopropylnaphthalen
- Naphthalene
- 1,3-Diisopropylnaphthalene
- 1,4-Diisopropylnaphthalene
- 3,7-di-tert-butylnaphthalene-1,5-disulphonic acid
- 1,5-DIISOPROPYLNAPHTHALENE SPECIALITY CHEMICALS
- 2,6-DIISOPROPYLNAPHTHALENE SOLUTION 100UG/ML IN ACETONITRILE 1ML
- 2,3-diisopropylnaphthalene
- 1,2-Diisopropylnaphthalene
- 1,6-Diisopropylnaphthalene
- 1,7-diisopropylnaphthalene