2,6-DIISOPROPYLNAPH...

2,6-DIISOPROPYLNAPHTHALENE

2,6-DIISOPROPYLNAPHTHALENE

Min.Order / FOB Price:Get Latest Price

1 Gram

Negotiable

  • Min.Order :1 Gram
  • Purity: 99% purity
  • Payment Terms : T/T,,MoneyGram,Other

Keywords

2,6-DIISOPROPYLNAPHTHALENE 24157-81-1 99% purity

Quick Details

  • Appearance:powder
  • Application:intermediate
  • PackAge:accroding to the need
  • ProductionCapacity:100|Kilogram|Day
  • Storage:Sealed in dry,Room Temperature
  • Transportation:air,sea and courier

Superiority:

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            
           

Details:

2,6-DIISOPROPYLNAPHTHALENE Chemical Properties
Melting point     67-70 °C
Boiling point     279.3 °C
density     0.9560 (estimate)
refractive index     1.5774 (estimate)
RTECS     QJ1536000
Fp     140 °C
Specific Gravity    0.968
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
MSDS Information
Provider    Language
ACROS    English
ALFA    English
2,6-DIISOPROPYLNAPHTHALENE Usage And Synthesis
Chemical Properties    beige crystalline platelets
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.                  
2,6-DIISOPROPYLNAPHTHALENE Preparation Products And Raw materials
Preparation Products    2,6-NAPHTHALENEDICARBOXYLIC ACID                

Related Searches

Confirm to collect the product to my collection?

OKCancel

About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia

Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog

©2008 LookChem.com,License: ICP

NO.:Zhejiang16009103

complaints:service@lookchem.com Desktop View