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2,6-DIISOPROPYLNAPHTHALENE

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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
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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)
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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

  • Language:English Provider:ACROS
  • Language:English Provider:ALFA
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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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