2,2,6,6-Tetramethylpiperidine

99%

Reagent Code: #238112
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CAS Number 768-66-1

science Other reagents with same CAS 768-66-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 141.25 g/mol
Formula C₉H₁₉N
badge Registry Numbers
MDL Number MFCD00005985
thermostat Physical Properties
Melting Point -59 °C
Boiling Point 152 °C
inventory_2 Storage & Handling
Density 0.837 g/mL
Storage Room temperature

description Product Description

Used primarily as a precursor in the synthesis of hindered amine light stabilizers (HALS), this compound plays a critical role in protecting polymers and coatings from degradation caused by ultraviolet (UV) light. Its derivatives help prevent photo-oxidative damage in plastics, paints, and adhesives, significantly extending the lifespan of outdoor materials such as polyolefins, automotive finishes, and agricultural films. Due to its stable amine structure, it effectively scavenges free radicals formed under UV exposure, reducing cracking, fading, and loss of mechanical strength. It is also employed in organic synthesis as a building block for specialty amines and nitroxyl radicals used in catalysis and analytical chemistry.

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Size Availability Unit Price Quantity
inventory 5ml
10-20 days ฿440.00
inventory 25ml
10-20 days ฿630.00
inventory 100ml
10-20 days ฿1,580.00
inventory 500ml
10-20 days ฿6,900.00

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2,2,6,6-Tetramethylpiperidine
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Used primarily as a precursor in the synthesis of hindered amine light stabilizers (HALS), this compound plays a critical role in protecting polymers and coatings from degradation caused by ultraviolet (UV) light. Its derivatives help prevent photo-oxidative damage in plastics, paints, and adhesives, significantly extending the lifespan of outdoor materials such as polyolefins, automotive finishes, and agricultural films. Due to its stable amine structure, it effectively scavenges free radicals formed under UV exposure, reducing cracking, fading, and loss of mechanical strength. It is also employed in organic synthesis as a building block for specialty amines and nitroxyl radicals used in catalysis and analytical chemistry.
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