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  • 1,1,3,3-Tetramethylguanidine, 99%, Thermo Scientific Chemicals

    A12314.AC

      CAT NUM
      PRODUCT NAME
      Pack Size
      PRICE
      QUANTITY
       
      CAT NUM: A12314.AC
      1,1,3,3-Tetramethylguanidine, 99%, Thermo Scientific Chemicals
      Pack Size: 25ML
      PRICE: 
      CAT NUM: A12314.AE
      1,1,3,3-Tetramethylguanidine, 99%, Thermo Scientific Chemicals
      Pack Size: 100ML
      PRICE: 
      CAT NUM: A12314.AP
      1,1,3,3-Tetramethylguanidine, 99%, Thermo Scientific Chemicals
      Pack Size: 500ML
      PRICE: 

      CAS Number
      80-70-6
      Hazard Class
      8
      Pack Size
      25ML, 100ML, 500ML
      Molecular Formula
      C5 H13 N3
      Molecular Weight
      115.18
      MFCD
      00008323
      Density
      0.918
      UN Number
      2920
      Flash Point
      60
      Storage Temp
      RT
      Brand
      Thermo Scientific - Alfa Aesar

      1,1,3,3-Tetramethylguanidine is employed as a polyurethane foam catalyst, as an accelerator for the syntheses of polysulfured rubber. It is also used as a strong base in the photochemical (couplers) and in the pharmaceutical (steroids) industries. It is essential for the preparation of alkyl nitriles from alkyl halides and 3'-alkylthymidines from 3'-nitrothymidines. It serves as an efficient and selective catalyst for the benzoylation of alcohols. It replaces the expensive bases 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) and 1,5-Diazabicyclo[4.3.0]non-5-ene (DBN) in organic synthesis.

      This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.


      Applications
      1,1,3,3-Tetramethylguanidine is employed as a polyurethane foam catalyst, as an accelerator for the syntheses of polysulfured rubber. It is also used as a strong base in the photochemical (couplers) and in the pharmaceutical (steroids) industries. It is essential for the preparation of alkyl nitriles from alkyl halides and 3′-alkylthymidines from 3′-nitrothymidines. It serves as an efficient and selective catalyst for the benzoylation of alcohols. It replaces the expensive bases 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) and 1,5-Diazabicyclo[4.3.0]non-5-ene (DBN) in organic synthesis.

      Solubility
      Miscible with water.

      Notes
      Air sensitive. Incompatible with strong oxidizing agents, mineral and organic acids, carbon dioxide. Keep away from sources of ignition.
      Certifications
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