- Product Details
Keywords
- 2,6-DIISOPROPYLNAPHTHALENE
- 24157-81-1
- 99% purity
Quick Details
- ProName: 2,6-DIISOPROPYLNAPHTHALENE
- CasNo: 24157-81-1
- Molecular Formula: C16H20
- Appearance: powder
- Application: intermediate
- DeliveryTime: in stock
- PackAge: accroding to the need
- Port: Shanghai Port
- ProductionCapacity: 100 Kilogram/Day
- Purity: 99% purity
- Storage: Sealed in dry,Room Temperature
- Transportation: air,sea and courier
- LimitNum: 1 Gram
- Grade: Industrial Grade,Pharma Grade,Electron...
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