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Home > Products >  MCMCAS NO.:598-55-0

MCMCAS NO.:598-55-0 CAS NO.598-55-0

  • FOB Price: USD: 1.00-2.00 /Kilogram Get Latest Price
  • Min.Order: 1 Gram
  • Payment Terms: L/C,D/A,D/P,T/T,MoneyGram,Other
  • Available Specifications:

    first class(1-10)Kilogramfirst class(10-100)Kilogram

  • Product Details

Keywords

  • MCM
  • p110-alpha
  • CARBAMIC ACID METHYL ESTER

Quick Details

  • ProName: MCMCAS NO.:598-55-0
  • CasNo: 598-55-0
  • Molecular Formula: C2H5NO2
  • Appearance: white powder
  • Application: Pharmaceutical intermediates
  • DeliveryTime: In stock
  • PackAge: bag
  • Port: China main port
  • ProductionCapacity: 10000 Gram/Day
  • Purity: 0.99
  • Storage: Room temperature
  • Transportation: By Sea/Air/DHL
  • LimitNum: 1 Gram
  • Heavy metal: N/A
  • Grade: Industrial Grade
  • first class: 1-10

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8) all your money be refund immediately if quality issue happens.

Details

Chemical Properties WHITE ADHERING CRYSTALS
Definition ChEBI: A carbamate ester resulting from the formal condensation of the carboxy group of carbamic acid with methanol.
General Description White crystals.
Air & Water Reactions Water soluble.
Reactivity Profile Methyl carbamate is a carbamate ester. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates.
Fire Hazard Flash point data for Methyl carbamate are not available; however, Methyl carbamate is probably combustible.
Safety Profile Poison by ingestion and intraperitoneal routes. Questionable carcinogen with experimental carcinogenic and tumorigenic data. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx. See also CARBAMATES.
Purification Methods Crystallise the carbamate from *benzene or distil it. [Beilstein 3 H 21.]

 

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