369497

N,N,N′,N′′,N′′-Pentamethyldiethylenetriamine

99%

• Synonym(s): PMDETA, PMDTA
• Linear Formula: [(CH₃)₂NCH₂CH₂]₂NCH₃
• CAS Number: 3030-47-5
• Molecular Weight: 173.30
• UNSPSC Code: 12162002
• NACRES: NA.23
• PubChem Substance ID: 24862979
• EC Number: 221-201-1
• Beilstein/REAXYS Number: 1741396
• MDL number: MFCD00014876

Properties

• vapor pressure: 0.23 mmHg ( 20 °C)
• Quality Segment: 300
• assay: 99%
• form: liquid
• autoignition temp.: 311 °F
• expl. lim.: 5.6 %
• refractive index: n20/D 1.442 (lit.)
• bp: 198 °C (lit.)
• mp: −20 °C (lit.)
• density: 0.83 g/mL at 25 °C (lit.)
• SMILES string: CN(C)CCN(C)CCN(C)C
• InChI: 1S/C9H23N3/c1-10(2)6-8-12(5)9-7-11(3)4/h6-9H2,1-5H3
• InChI key: UKODFQOELJFMII-UHFFFAOYSA-N

Description

General 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.

Application

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.[1]
• An initiator to grow polystyrene chains to prepare polyolefin-polystyrene copolymers.[2]

Safety Information

• pictograms: GHS06,GHS05
• signalword: Danger
• hcodes: H302,H311,H314
• pcodes: P270 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
• Hazard Classifications: Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
• Storage Class: 6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
• wgk: WGK 2
• flash_point_f: 168.8 °F - closed cup
• flash_point_c: 76 °C - closed cup
• ppe: Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter