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Home > Products >  1,4-Naphthalenedione,2-hydroxy-

1,4-Naphthalenedione,2-hydroxy- CAS NO.83-72-7

  • Min.Order: 1 Kilogram
  • Payment Terms: L/C,T/T,MoneyGram,Other
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  • 1,4-Naphthalenedione,2-hydroxy- CAS83-72-7
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Quick Details

  • ProName: 1,4-Naphthalenedione,2-hydroxy-
  • CasNo: 83-72-7
  • Molecular Formula: C10H6O3
  • Appearance: Yellow crystal powder
  • Application: antifungal, sunscreen, antibacterial, ...
  • 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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2-Hydroxy-1,4-naphoquinone Chemical Properties
mp  192-195 °C (dec.)(lit.)
Colour Index  75480
Water Solubility  2 g/L (20 ºC)
Merck  14,5393
BRN  1565260
Stability: Stable. Combustible. Incompatible with strong oxidizing agents.
CAS DataBase Reference 83-72-7(CAS DataBase Reference)
NIST Chemistry Reference 1,4-Naphthalenedione, 2-hydroxy-(83-72-7)
EPA Substance Registry System 1,4-Naphthalenedione, 2-hydroxy-(83-72-7)
 
Safety Information
Hazard Codes  Xi,Xn
Risk Statements  36/37/38-68-36-22
Safety Statements  26-37/39-36/37/39-36
WGK Germany  3
RTECS  QL8200000
MSDS Information
Provider Language
2-Hydroxy-1,4-naphoquinone English
ACROS English
SigmaAldrich English
ALFA English
 
2-Hydroxy-1,4-naphoquinone Usage And Synthesis
Chemical Properties Yellow crystal powder
Usage antifungal, sunscreen, antibacterial, antineoplastic
General Description Yellow prisms or yellow powder.
Air & Water Reactions Insoluble in water.
Reactivity Profile Phenols, such as 2-Hydroxy-1,4-naphoquinone, 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.
Health Hazard ACUTE/CHRONIC HAZARDS: 2-Hydroxy-1,4-naphoquinone may be absorbed through the skin and can cause skin irritation.
Fire Hazard Flash point data for 2-Hydroxy-1,4-naphoquinone are not available but 2-Hydroxy-1,4-naphoquinone is probably combustible.
 
2-Hydroxy-1,4-naphoquinone Preparation Products And Raw materials
Preparation Products NILE RED
Raw materials Ammonium sulfamate-->1,4-Naphthoquinone-->1,2-NAPHTHOQUINONE

 

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