Nylon-6,6
(C₁₂H₂₂N₂O₂)ₙCite "Nylon-6,6"
Nylon-6,6. (n.d.). In Compound. Retrieved from /compound/nylon-66/
"Nylon-6,6." Compound, /compound/nylon-66/.
@misc{nylon-66, title={Nylon-6,6}, url={/compound/nylon-66/}}
IUPAC: Poly(hexamethylene adipamide)
CAS: 32131-17-2
Overview
Nylon-6,6 was the first commercially successful synthetic polymer, developed by Wallace Carothers at DuPont in 1935. It revolutionized the textile industry by replacing silk in stockings. It is a polyamide with excellent strength, elasticity, and abrasion resistance.
Composition
Uses
- • Textiles (stockings, clothing)
- • Automotive parts (gears, bearings)
- • Carpet fibers
- • Cable ties and fasteners
Fun Facts
- ✦ Nylon stockings were such a sensation that 4 million pairs sold on the first day in 1940
- ✦ The name 'nylon' is not an acronym — it was chosen arbitrarily by DuPont
Safety
- ⚠ Melts and can cause burns
- ⚠ Releases toxic fumes when burned
Properties
- Type
- polymer
- State
- solid
- Molar Mass
- 226.32 g/mol
- Density
- 1.1400 g/cm³
- Melting Point
- 263.0 °C
- Solubility
- insoluble
Also Known As
Nylon
Nylon-6,6
Frequently Asked Questions
What is Nylon-6,6?
Nylon-6,6 ((C₁₂H₂₂N₂O₂)ₙ) is a polymer compound with the IUPAC name Poly(hexamethylene adipamide).
What is the molecular weight of Nylon-6,6?
Nylon-6,6 has a molar mass of 226.318 g/mol.
What state is Nylon-6,6 at room temperature?
Nylon-6,6 is a solid at room temperature.
Is Nylon-6,6 organic or inorganic?
Nylon-6,6 is classified as an inorganic compound.
What elements make up Nylon-6,6?
Nylon-6,6 ((C₁₂H₂₂N₂O₂)ₙ) is composed of Hydrogen (H), Carbon (C), Nitrogen (N), Oxygen (O).