2,6-Diisopropylnaphthalin

Bezeichnung:2,6-Diisopropylnaphthalin

CAS-Nr24157-81-1

Englisch Name:2,6-DIISOPROPYLNAPHTHALENE

CBNumberCB1702468

SummenformelC16H20

Molgewicht212.33

MOL-Datei24157-81-1.mol

Synonyma

2,6-Diisopropylnaphthalin

2,6-Diisopropylnaphthalin physikalisch-chemischer Eigenschaften

Schmelzpunkt	67-70 °C
Siedepunkt	279.3 °C
Dichte	0.9560 (estimate)
Dampfdruck	0.08Pa at 25℃
Brechungsindex	1.5774 (estimate)
RTECS-Nr.	QJ1536000
Flammpunkt	140 °C
Löslichkeit	Acetonitrile (Slightly), Chloroform (Slightly), Methanol
Aggregatzustand	powder to crystal
Farbe	White to Almost white
Wichte	0.968
Wasserlöslichkeit	1mg/L at 25℃
LogP	6.5 at 25℃
CAS Datenbank	24157-81-1(CAS DataBase Reference)
EPA chemische Informationen	2,6-Diisopropylnaphthalene (24157-81-1)

Sicherheit

Kennzeichnung gefährlicher	Xn,N
R-Sätze:	22-50/53
S-Sätze:	24/25-61-60
RIDADR	3077
TSCA	Yes
HazardClass	9
PackingGroup	III
HS Code	29029090

Gefahreninformationscode (GHS)

2,6-DIISOPROPYLNAPHTHALENE Chemische Eigenschaften,Einsatz,Produktion Methoden

S-Sätze Betriebsanweisung:
S24/25:Berührung mit den Augen und der Haut vermeiden.
Chemische Eigenschaften
beige crystalline platelets
Verwenden
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.
Allgemeine Beschreibung
Clear yellowish brown liquid with a faint sweet odor.
Air & Water Reaktionen
Insoluble in water.
Reaktivität anzeigen
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.
Brandgefahr
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 Upstream-Materialien And Downstream Produkte

2,6-Diisopropylnaphthalin Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

24157-81-1, 2,6-DIISOPROPYLNAPHTHALENE Verwandte Suche:

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