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Butylphenol, Isomere mixture

Butylphenol, Isomere mixture Struktur
28805-86-9
CAS-Nr.
28805-86-9
Englisch Name:
Butylphenol, Isomere mixture
Synonyma:
Phenol, butyl-;Einecs 249-246-2;Butylphenols, solid;Butylphenols, liquid;Butylphenol, isomer mixture
CBNumber:
CB4875213
Summenformel:
C10H14O
Molgewicht:
150.21756
MOL-Datei:
28805-86-9.mol

Butylphenol, Isomere mixture Eigenschaften

Schmelzpunkt:
98.9°C
Siedepunkt:
239.5°C (estimate)
Dichte
0.9108 (rough estimate)
Brechungsindex
1.4890 (estimate)
Wasserl?slichkeit
399.8mg/L(25 ºC)
EPA chemische Informationen
Phenol, butyl- (28805-86-9)

Sicherheit

Butylphenol, Isomere mixture Chemische Eigenschaften,Einsatz,Produktion Methoden

Chemische Eigenschaften

The butylphenols include several isomers. Solid butylphenols (28805-86-9) generally have properties similar to the above:

Allgemeine Beschreibung

Butyl phenol (para-tert) is a white crystalline solid. Butylphenol, Isomere mixture is insoluble in water. Butylphenol, Isomere mixture may burn though Butylphenol, Isomere mixture may require some effort to ignite. Butylphenol, Isomere mixture is corrosive to metals and tissue. Butylphenol, Isomere mixture is used to make other chemicals.

Air & Water Reaktionen

Insoluble in water.

Reaktivit?t anzeigen

Phenols, such as BUTYLPHENOL, do not behave as organic alcohols, as one might guess from the presence of a hydroxyl (-OH) group in their structure. Instead, they react as weak organic acids. Phenols and cresols are much weaker as acids than common carboxylic acids (phenol has Ka = 1.3 x 10^[-10]). These materials are incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may ignite the gas. Heat is also generated by the acid-base reaction between phenols and bases. Such heating may initiate polymerization of the organic compound. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). The reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid.

Health Hazard

Inhalation of vapors causes irritation of respiratory system. Ingestion causes irritation of mouth and stomach. Contact with eyes causes burns. Contact with dry skin produces no significant irritation, but wet skin is subject to moderate irritation, even a mild burn.

m?gliche Exposition

Butylphenols may be used as intermediates in manufacturing varnish and lacquer resins; as a germicidal agent in detergent disinfectants; as a pour point depressant, in motor-oil additives; de-emulsifier for oil; soap-antioxidant, plasticizer, fumigant, and insecticide

Versand/Shipping

UN2430 Alkylphenols, solid, n.o.s. (including C2-C12 homologues), Hazard class: 8; Labels: 8— Corrosive material

Inkompatibilit?ten

Vapors may form explosive mixture with air. These phenol/cresol materials can react with oxidizers; reaction may be violent. Incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may cause the gas to ignite and explode. Heat is also generated by the acid-base reaction with bases; such heating may initiate polymerization of the organic compound. React with boranes, alkalies, aliphatic amines, amides, nitric acid, sulfuric acid. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). These reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid and can explode when heated. Many phenols form metal salts that may be detonated by mild shock

Butylphenol, Isomere mixture Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


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  • Butylphenol, isomer mixture
  • Butylphenols, liquid
  • Butylphenols, solid
  • Einecs 249-246-2
  • Phenol, butyl-
  • 28805-86-9
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