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 Structure
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 Gravity0.968
Water Solubility 1mg/L at 25℃
LogP6.5 at 25℃
CAS DataBase Reference24157-81-1(CAS DataBase Reference)
EPA Substance Registry System2,6-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
MSDS Information
ProviderLanguage
ACROS English
ALFA English
2,6-DIISOPROPYLNAPHTHALENE Usage And Synthesis
Chemical Propertiesbeige crystalline platelets
Uses2,6-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.
DefinitionChEBI: 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 DescriptionClear yellowish brown liquid with a faint sweet odor.
Air & Water ReactionsInsoluble in water.
Reactivity ProfileVigorous 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 HazardExposure can cause irritation of eyes, nose and throat.
Fire HazardSpecial 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 ExplosibilityNotclassified
2,6-DIISOPROPYLNAPHTHALENE Preparation Products And Raw materials
Preparation Products2,6-NAPHTHALENEDICARBOXYLIC ACID
2-[6-(1-hydroxy-1-methylethyl)-2-naphthyl]-2-propanol 2,6-Di-tert-butylnaphthalene 2,6-DIISOPROPYLNAPHTHALENE 1,7-diisopropylnaphthalene 1,8-diisopropylnaphthalene 3,7-di-tert-butylnaphthalene-1,5-disulphonic acid 1,3-Diisopropylnaphthalene Dibunate sodium 3,7-DI(TERT-BUTYL)-1,5-DINITRONAPHTHALENE 2,3-diisopropylnaphthalene 1,2-Diisopropylnaphthalene 2,6-DIISOPROPYLNAPHTHALENE SOLUTION 100UG/ML IN ACETONITRILE 1ML DIISOPROPYLNAPHTHALENE,Diisopropylnaphthalene: (Bis(isopropyl)naphthalene) 2,6-DI-TERT-BUTYLNAPHTHALENE DISULFONIC ACID, NA 1,6-Diisopropylnaphthalene sodium diisopropylnaphthalenesulphonate TIPS 2,6-DI-TERT-BUTYLNAPHTHALENE DISULFONIC ACID SODIUM SALT

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