Weight | 113.16 g/mol |
---|---|
Formula | C6H11NO |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
N-ISOPROPYLACRYLAMIDE (2210-25-5)
Score:
#153 in Materials science
,
#1143 in Physics
,
#3259 in Chemistry
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- Poly (N-isopropylacrylamide) : experiment, theory and application (Progress in Polymer Science, 1992)
- Solution Properties of Poly(N-isopropylacrylamide) (Journal of Macromolecular Science, Part A, 1968)
- Effect of comonomer hydrophilicity and ionization on the lower critical solution temperature of N-isopropylacrylamide copolymers (Macromolecules, 1993)
- A novel recovery system for cultured cells using plasma-treated polystyrene dishes grafted with poly(N-isopropylacrylamide) (Journal of Biomedical Materials Research, 1993)
- Phase transition of aqueous solutions of poly(N-isopropylacrylamide) and poly(N-isopropylmethacrylamide) (The Journal of Physical Chemistry, 1989)
- Preparation of aqueous latices with N-isopropylacrylamide (Colloids and Surfaces, 1986)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 -
SMILESCC(C)NC(=O)C=C
-
InChIKeyQNILTEGFHQSKFF-UHFFFAOYSA-N
- Pubchem - N-ISOPROPYLACRYLAMIDE
- Wikipedia - Poly(N-isopropylacrylamide)
Poly(N-isopropylacrylamide) (variously abbreviated PNIPA, PNIPAAm, NIPA, PNIPAA or PNIPAm) is a temperature-responsive polymer that was first synthesized in the 1950s. It can be synthesized from N-isopropylacrylamide which is commercially available. It is synthesized via free-radical polymerization and is readily functionalized making it useful in a variety of applications.
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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