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CS-W001157 4
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N1-(2-(Dimethylamino)ethyl)-N1,N2,N2-trimethylethane-1,2-diamine

  • CAS No. 3030-47-5

  • Cat. No. CS-0077160
  • Purity≥98%
  • MDL No.MFCD00014876

*For research and further manufacturing use only, not for direct human use.

N1-(2-(Dimethylamino)ethyl)-N1,N2,N2-trimethylethane-1,2-diamine|CS-0077160

Structure of 3030-47-5

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General Information

  • CAS No. 3030-47-5
  • Cat. No. CS-0077160
  • Purity ≥98%
  • MDL No. MFCD00014876
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₂₃N₃
  • Molecular Weight 173.30
  • Synonym(s) Pentamethyldiethylenetriamine
  • SMILES CN(C)CCN(CCN(C)C)C

Description

N,N,N,N,N-Pentamethyldiethylenetriamine (PMDETA) is an amine-based monomer compound that plays a crucial role in the field of polymers, particularly in the synthesis of TRPs- thermoresponsive polymers. PMDETA acts as a versatile ligand or catalyst in various polymerization reactions. It forms complexes with transition metals, which are utilized in the production of specialty polymers, block copolymers, and polymers with modified properties. These polymers find applications across a broad range of industries, including thermoplastics, elastomers, and coatings. When incorporated into the polymer structure, PMDETA helps impart thermoresponsive behavior to the final product, enabling reversible changes in solubility, conformation, or other physical properties in response to temperature variations. This makes PMDETA a valuable component in the synthesis and design of TRPs, which find uses in areas such as drug delivery systems, smart materials, and responsive coatings.N,N,N,N,N Pentamethyldiethylenetriamine can be used as:A catalyst in the synthesis of multifunctional silicone acrylate prepolymers for use in UV-curable coatings.A multifunctional initiating and cross-linking agent in the synthesis of polyacrylamide hydrogels. It improves the mechanical properties of the hydrogels, such as toughness and resilience, without compromising their biocompatibility.An organocatalyst in ring-opening polymerization (ROP) of trimethylene carbonate. This catalyst can be easily removed after the reaction compared to metal catalysts.A catalyst along with CuBr to synthesize a series of side-chain azobenzene poly(meth)acrylates via the atom transfer radical polymerization(ATRP) technique.An initiator to grow polystyrene chains to prepare polyolefin-polystyrene copolymers.

Synthesis

  • Route1
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    • In-stock
      N1-(2-(Dimethylamino)ethyl)-N1,N2,N2-trimethylethane-1,2-diamine|CS-0077160
      3030-47-5
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      106-64-9
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      75-50-3

    References

    • Journal of the American Chemical Society, , vol. 107, # 2 p. 361 - 369
  • Route2
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      110-18-9
    • ~%
    • null|null
      106-58-1
    • null|null
      104-19-8
    • In-stock
      N1-(2-(Dimethylamino)ethyl)-N1,N2,N2-trimethylethane-1,2-diamine|CS-0077160
      3030-47-5
    • null|null
      106-64-9
    • null|null
      75-50-3

    References

    • Journal of the American Chemical Society, , vol. 107, # 2 p. 361 - 369
  • Route3
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      50-00-0
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      111-40-0
    • ~87%
    • In-stock
      N1-(2-(Dimethylamino)ethyl)-N1,N2,N2-trimethylethane-1,2-diamine|CS-0077160
      3030-47-5

    References

    • Devinsky; Masarova; Lacko; Mlynarcik Collection of Czechoslovak Chemical Communications, 1984 , vol. 49, # 12 p. 2819 - 2827

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS05,GHS06
Signal Word : Danger
UN#: 2922
Class : 8(6.1)
Packing Group : Ⅱ
Hazard Statements : H302-H311-H314
Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P302+P352-P304+P340-P330-P361+P364-P363-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   9.72
  • LogP   0.0414
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   6

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