3-butylphenol

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Factory supply 3-butylphenol 4074-43-5 with low price

  • Molecular Formula: C10H14 O
  • Molecular Weight: 150.221
  • Vapor Pressure: 0.016mmHg at 25°C 
  • Melting Point: 46.81°C (estimate) 
  • Refractive Index: 1.5094 (estimate) 
  • Boiling Point: 247.7°Cat760mmHg 
  • Flash Point: 122.7°C 
  • PSA: 20.23000 
  • Density: 0.977g/cm3 
  • LogP: 2.73480 

3-butylphenol(Cas 4074-43-5) Usage

Potential Exposure

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

Shipping

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

Incompatibilities

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

InChI:InChI=1/C10H14O/c1-2-3-5-9-6-4-7-10(11)8-9/h4,6-8,11H,2-3,5H2,1H3

4074-43-5 Relevant articles

Scalable Negishi Coupling between Organozinc Compounds and (Hetero)Aryl Bromides under Aerobic Conditions when using Bulk Water or Deep Eutectic Solvents with no Additional Ligands

Dilauro, Giuseppe,Azzollini, Claudia S.,Vitale, Paola,Salomone, Antonio,Perna, Filippo M.,Capriati, Vito

supporting information, p. 10632 - 10636 (2021/04/09)

Pd-catalyzed Negishi cross-coupling reac...

Copper-catalyzed oxidative aromatization of 2-cyclohexen-1-ones to phenols in the presence of catalytic hydrogen bromide under molecular oxygen

Kikushima, Kotaro,Nishina, Yuta

, p. 20150 - 20156 (2013/11/06)

Catalytic oxidative aromatization has be...

A 'meta effect' in the fragmentation reactions of ionised alkyl phenols and alkyl anisoles

Bouchoux, Guy,Sablier, Michel,Miyakoshi, Tetsuo,Honda, Takashi

experimental part, p. 539 - 546 (2012/09/22)

The competition between benzylic cleavag...

The separation and synthesis of lipidic 1,2- and 1,3-diols from natural phenolic lipids for the complexation and recovery of boron

Tyman, John H.P.,Mehet, Satinderjit K.

, p. 177 - 199 (2007/10/03)

A study has been made of the semi-synthe...

4074-43-5 Process route

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Conditions
Conditions Yield
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95.8%
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Conditions
Conditions Yield
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97%

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