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4074-43-5

4074-43-5 Structure

4074-43-5 Structure
IdentificationBack Directory
[Name]

3-butylphenol
[CAS]

4074-43-5
[EINECS(EC#)]

223-790-0
[Molecular Formula]

C10H14O
[MOL File]

4074-43-5.mol
[Molecular Weight]

150.218
Chemical PropertiesBack Directory
[Appearance]

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

46.81°C (estimate)
[Boiling point ]

247°C
[density ]

0.9740
[refractive index ]

1.5094 (estimate)
Hazard InformationBack Directory
[Chemical Properties]

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

If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least 15 minutes, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR if heart action has stopped. Transfer promptly to a medical facility. When this chemical has been swallowed, get medical attention. Give large quantities of water and induce vomiting. Do not make an unconscious person vomit
[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
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