2,6-DIISOPROPYLNAPHTHALENE

2,6-DIISOPROPYLNAPHTHALENE Suppliers list
Company Name:J & K SCIENTIFIC LTD.  
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Products Intro: Product Name:2,6-Diisopropylnaphthalene
CAS:24157-81-1
Purity:99% Package:100G,25G
Company Name:Meryer (Shanghai) Chemical Technology Co., Ltd.  
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Products Intro: Product Name:2,6-Diisopropylnaphthalene
CAS:24157-81-1
Purity:>99.0%(GC) Package:25g;500g Remarks:D1598
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Products Intro: Product Name:2,6-Diisopropylnaphthalene
CAS:24157-81-1
Purity:99.0%(GC) Package:500G;25G
Company Name:Energy Chemical  
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Products Intro: Product Name:2,6-DIISOPROPYLNAPHTHALENE
CAS:24157-81-1
Purity:99% Package:1kg,250g,50g
Company Name:Adamas Reagent, Ltd.   
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Products Intro: Product Name:2,6-Diisopropylnaphthalene
CAS:24157-81-1
Purity:98%+ Package:25g;100g
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-Diisopropylnaphthalene,99%
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
mp 67-70 °C
bp 279.3 °C
Fp 140 °C
CAS DataBase Reference24157-81-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,N
Risk Statements 22-50/53
Safety Statements 24/25-61-60
RIDADR 3077
HazardClass 9
PackingGroup III
MSDS Information
ProviderLanguage
ACROS English
ALFA English
2,6-DIISOPROPYLNAPHTHALENE Usage And Synthesis
Chemical Propertiesbeige crystalline platelets
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.
2,6-DIISOPROPYLNAPHTHALENE Preparation Products And Raw materials
Preparation Products2,6-NAPHTHALENEDICARBOXYLIC ACID
Tag:2,6-DIISOPROPYLNAPHTHALENE(24157-81-1) Related Product Information
1,5-DIISOPROPYLNAPHTHALENE SPECIALITY CHEMICALS 2,6-DIISOPROPYLNAPHTHALENE SOLUTION 100UG/ML IN ACETONITRILE 1ML 2,3-diisopropylnaphthalene 1,2-Diisopropylnaphthalene DIISOPROPYLNAPHTHALENE,Diisopropylnaphthalene: (Bis(isopropyl)naphthalene) 1,6-Diisopropylnaphthalene 1,7-diisopropylnaphthalene 1,8-diisopropylnaphthalene sodium diisopropylnaphthalenesulphonate 1,3-Diisopropylnaphthalene 2-[6-(1-hydroxy-1-methylethyl)-2-naphthyl]-2-propanol 3,7-DI(TERT-BUTYL)-1,5-DINITRONAPHTHALENE TIPS Dibunate sodium 2,6-DI-TERT-BUTYLNAPHTHALENE DISULFONIC ACID SODIUM SALT 2,6-DI-TERT-BUTYLNAPHTHALENE DISULFONIC ACID, NA 3,7-di-tert-butylnaphthalene-1,5-disulphonic acid 2,6-Di-tert-butylnaphthalene