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ChemicalBook--->CAS DataBase List--->24157-81-1

24157-81-1

24157-81-1 Structure

24157-81-1 Structure
IdentificationMore
[Name]

2,6-DIISOPROPYLNAPHTHALENE
[CAS]

24157-81-1
[Synonyms]

2,6-BIS(1-METHYLETHYL)-NAPHTHALENE
2,6-DIISOPROPYLNAPHTHALENE
2,6-bis(1-methylethyl)-naphthalen
Naphthalene, 2,6-bis(1-methylethyl)-
Naphthalene, 2,6-diisopropyl-
2,6-DIISOPRYLNAPHTHALENE
2,6-DIISOPROPYL NAHPTHALENE TECHNICAL
[EINECS(EC#)]

246-045-1
[Molecular Formula]

C16H20
[MDL Number]

MFCD00021648
[Molecular Weight]

212.33
[MOL File]

24157-81-1.mol
Chemical PropertiesBack Directory
[Appearance]

beige crystalline platelets
[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 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)
Safety DataBack Directory
[Hazard Codes ]

Xn,N
[Risk Statements ]

22-50/53
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
[RIDADR ]

3077
[TSCA ]

Yes
[HazardClass ]

9
[PackingGroup ]

III
[HS Code ]

29029090
Raw materials And Preparation ProductsBack Directory
[Preparation Products]

2,6-NAPHTHALENEDICARBOXYLIC ACID
Hazard InformationBack Directory
[General Description]

Clear yellowish brown liquid with a faint sweet odor.
[Reactivity Profile]

Vigorous reactions, sometimes amounting to explosions, can result from the contact between aromatic hydrocarbons, such as DIISOPROPYL NAPHTHALENE(24157-81-1), 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].
[Air & Water Reactions]

Insoluble in water.
[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.
[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.
[Flammability and Explosibility]

Notclassified
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2,6-Diisopropylnaphthalene, 99%(24157-81-1)
[Alfa Aesar]

2,6-Diisopropylnaphthalene, 99%(24157-81-1)
[TCI AMERICA]

2,6-Diisopropylnaphthalene,>99.0%(GC)(24157-81-1)
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