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Home > Products >  Phenol,4-(1,1-dimethylpropyl)-

Phenol,4-(1,1-dimethylpropyl)- CAS NO.80-46-6

  • Min.Order: 1 Kilogram
  • Payment Terms: L/C,T/T,MoneyGram,Other
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Quick Details

  • ProName: Phenol,4-(1,1-dimethylpropyl)-
  • CasNo: 80-46-6
  • Molecular Formula: C11H16O
  • Appearance: White little spiculate crystal
  • Application: Used in organic synthesis
  • DeliveryTime: 15 days after order confirmed
  • PackAge: 1kg/bag, 1kg/drum or 25kg/drum or as p...
  • Port: Shanghai, Ningbo, Tianjin, etc
  • ProductionCapacity: 1 Metric Ton/Month
  • Purity: 99%
  • Storage: Stored in cool, dry and ventilation pl...
  • Transportation: by courier door to door or by sea
  • LimitNum: 1 Kilogram

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4-tert-Amylphenol Chemical Properties
mp  88-89 °C(lit.)
bp  255 °C(lit.)
density  0,96 g/cm3
Fp  111 °C
Water Solubility  37 mg/L (20 ºC)
Merck  14,7142
Stability: Stable. Incompatible with acid chlorides, acid anhydrides, strong oxidizing agents.
CAS DataBase Reference 80-46-6(CAS DataBase Reference)
NIST Chemistry Reference Phenol, 4-(1,1-dimethylpropyl)-(80-46-6)
EPA Substance Registry System Phenol, 4-(1,1-dimethylpropyl)-(80-46-6)
 
Safety Information
Hazard Codes  C,N
Risk Statements  21/22-34-51/53
Safety Statements  26-27-36/37/39-45-61
RIDADR  UN 2430 8/PG 2
WGK Germany  2
RTECS  SM6825000
HazardClass  8
PackingGroup  III
Hazardous Substances Data 80-46-6(Hazardous Substances Data)
MSDS Information
Provider Language
4-tert-Amylphenol English
SigmaAldrich English
ACROS English
ALFA English
 
4-tert-Amylphenol Usage And Synthesis
Chemical Properties solid
General Description Colorless needles or beige solid.
Air & Water Reactions Insoluble in water.
Reactivity Profile Phenols, such as 4-tert-Amylphenol, 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. Nitrated phenols often explode when heated. Many of them form metal salts that tend toward detonation by rather mild shock. 4-tert-Amylphenol can react with oxidizing materials.
Health Hazard ACUTE/CHRONIC HAZARDS: 4-tert-Amylphenol is toxic by ingestion and can be absorbed through the skin. Hazardous fumes are evolved when 4-tert-Amylphenol is heated to decomposition.
Fire Hazard 4-tert-Amylphenol is combustible.
 
4-tert-Amylphenol Preparation Products And Raw materials
Raw materials Aluminium chloride hexahydrate

 

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