Inhibitor 701 99% CAS#2226-96-2
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Chemical Name:Inhibitor 701 99%
CAS No.:2226-96-2
Molecular Formula:C9H18NO2*
Molecular weight:172.24
Sample: Available
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Products Description of Inhibitor 701 99% CAS#2226-96-2
Inhibitor 701 is a nitroxide free radical inhibitor, which is suitable for preventing the self-polymerization of olefins and unsaturated monomers during production, separation, refining, storage and transportation, and controlling and regulating the degree of polymerization of olefins and their derivatives in organic synthesis reactions2. The inhibitory performance of Inhibitor 701 is better than that of phenols, aromatic amines, ethers, quinones and nitro compounds, and can replace hydroquinone, which has a greater environmental pollution. Its inhibitory effect is about 4 times that of hydroquinone2.
4-Hydroxy-2,2,6,6-tetramethyl-piperidinooxy Chemical Properties
Melting point | 69-71 °C(lit.) |
Boiling point | 302.58°C (rough estimate) |
density | 1.0402 (rough estimate) |
vapor pressure | 0.025Pa at 20℃ |
refractive index | 1.4350 (estimate) |
Fp | 146°(295°F) |
storage temp. | 2-8°C |
solubility | 1670g/l |
form | Crystals or Crystalline Powder |
pka | 5.07[at 20 ℃] |
color | Orange |
PH | 8.2 (20g/l, H2O, 20℃) |
Water Solubility | soluble |
Merck | 14,9141 |
BRN | 1422990 |
Stability: | Stable. Incompatible with strong oxidizing agents. |
InChIKey | FAPCFNWEPHTUQK-UHFFFAOYSA-N |
LogP | 0.56 at 25℃ |
CAS DataBase Reference | 2226-96-2(CAS DataBase Reference) |
NIST Chemistry Reference | 1-Piperidinyloxy, 4-hydroxy-2,2,6,6-tetramethyl-(2226-96-2) |
EPA Substance Registry System | 1-Piperidinyloxy, 4-hydroxy-2,2,6,6-tetramethyl- (2226-96-2) |
Safety Information
Hazard Codes | Xn,Xi |
Risk Statements | 22-36/37/38-36/38 |
Safety Statements | 26-36-37/39-36/37/39-27 |
WGK Germany | 1 |
RTECS | TN8991000 |
TSCA | Yes |
HS Code | 29333999 |
Hazardous Substances Data | 2226-96-2(Hazardous Substances Data) |
Toxicity | LD50 oral in rat: 1053mg/kg |
Product Application of Inhibitor 701 99% CAS#2226-96-2
Inhibitor 701 has a good inhibitory effect on acrylates, methacrylates, acrylic acid, acrylonitrile, styrene, and butadiene. Its inhibitory performance is better than that of inhibitors such as phenols, aromatic amines, ethers, quinones, and nitro compounds. Inhibitor 701 can be used as a spin label for studying biological compounds and polymers; a spin labeling reagent for identifying antagonist and agonist binding sites of NK1 receptors, and can also be used for electron spin resonance spectroscopy to determine the generation of reactive oxygen species in the myocardium; TEMPOL can protect cells overexpressing CYP2E1 from toxic damage caused by arachidonic acid; it can be used to prepare fluorine-labeled TEMPO derivatives by derivatizing TEMPO propargyl ether and then reacting with fluorine azide in a "click" reaction; it can be used as an efficient catalyst in the reaction of oxidizing alcohols with bleach. It is used to prevent the self-polymerization of olefin monomers during production, separation, refining, storage or transportation, and to control and regulate the degree of polymerization of olefins and their derivatives.
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