UV 327
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UV 327
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CAS No:
3864-99-1
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Formula:
C20H24ClN3O
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Chemical Name:
UV 327
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Synonyms:
Phenol,2-(5-chloro-2H-benzotriazol-2-yl)-4,6-bis(1,1-dimethylethyl)-;Phenol,2,4-di-tert-butyl-6-(5-chloro-2H-benzotriazol-2-yl)-;2-(5-Chloro-2H-benzotriazol-2-yl)-4,6-bis(1,1-dimethylethyl)phenol;2-(3,5-Di-tert-butyl-2-hydroxyphenyl)-5-chlorobenzotriazole;2-(2′-Hydroxy-3′,5′-di-tert-butylphenyl)-5-chlorobenzotriazole;Tinuvin 327;2-(2-Hydroxy-3,5-di-tert-butylphenyl)-5-chlorobenzotriazole;2-(3,5-Di-tert-butyl-2-hydroxyphenyl)-5-chloro-2H-benzotriazole;2-(2-Hydroxy-3,5-di-tert-butylphenyl)-5-chloro-2H-benzotriazole;2,4-Di-tert-butyl-6-(5-chloro-2H-benzotriazol-2-yl)phenol;5-Chloro-2-(2-hydroxy-3,5-di-tert-butylphenyl)benzotriazole;5-Chloro-2-(3,5-di-tert-butyl-2-hydroxyphenyl)benzotriazole;5-Chloro-2-(3′,5′-di-tert-butyl-2′-hydroxyphenyl)benzotriazole;UV 2;5-Chloro-2-(3,5-di-tert-butyl-2-hydroxyphenyl)-2H-benzotriazole;UV 327;UV-Chek AM 607;Viosorb 580;Kemisorb 72;LA 34;ADK Stab LA 34;5-Chloro-2-(2-hydroxy-3,5-di-tert-butylphenyl)-2H-benzotriazole;Cyasorb UV 5357;2-(3′,5′-Di-tert-butyl-2′-hydroxyphenyl)-5-chlorobenzotriazole;Seesorb 702;UV 2 (UV stabilizer);Hisorp 327;2,4-Di-tert-butyl-6-(5-chlorobenzotriazol-2-yl)phenol;TNV 327;Mark LA 34;Lowilite 27;Eversorb 75;Hisorb 327;Antioxidant 327;Songsorb 3270;2,4-Di-(tert-butyl)-6-(5-chloro-2H-benzo[d][1,2,3]triazol-2-yl)phenol;Chiguard 327;UVP 327;Light stabilizer 327;Sunsorb 327;2,4-Ditert-butyl-6-(5-chlorobenzotriazol-2-yl)phenol;60712-40-5;102257-29-4;106085-69-2;114625-87-5;153613-74-2;188025-33-4;189456-66-4;659718-57-7;796971-90-9;1350838-92-4;1399293-74-3
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CAS No:
Description
Solid
DryPowder|Solid
5-Chloro-2-(3,5-di-tert-butyl-2-hydroxyphenyl)-2H-benzotriazole is a member of triazoles.
Characteristics
50.9
6.9
DryPowder
1.2±0.1 g/cm3
147.6-148.8 °C @ Solvent: Methanol
469.2°C at 760 mmHg
234°C
1.596
0.02628 mg/L @ 25 °C (est)
Safety Information
9
3077
2
36/37/38
26-36
3425000
Xi
P261-P305 + P351 + P338
H315-H319-H335
|Warning|H373 (92.82%): Causes damage to organs through prolonged or repeated exposure [Warning Specific target organ toxicity, repeated exposure]|P260, P273, P314, and P501|Aggregated GHS information provided by 606 companies from 24 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|Not Classified
UV 327 Use and Manufacturing
The p-chloro-o-nitroaniline is diazotized with sodium nitrite, and then coupled with 2, 4-di-tert-butylphenol. The coupling product is reduced by adding zinc powder in an alcohol-alkali medium to obtain a crude product, and then to be purified to obtain a finished product. Raw material consumption (kg/t) phenol (99%) 2201 isobutylene (99.5%) 2615 (used to synthesize 2, 4-di-tert-butylphenol) p-chloro-o-nitroaniline (60%) 2044 ethyl acetate (98% ) 6765 (for purification)
Excellent light stabilizer, good synergistic effect when used with antioxidant. The product has low volatility and good compatibility with resin. It is suitable for polypropylene, polyethylene, polyoxymethylene and polymethyl methacrylate, etc., especially for polypropylene fiber. Especially suitable for polyethylene and polypropylene, but also for polyoxymethylene, polymethyl methacrylate, polyurethane and various coatings
Photosensitive chemicals
25,000 - 100,000 lb
Plastic material and resin manufacturing|Phenol, 2-(5-chloro-2H-benzotriazol-2-yl)-4,6-bis(1,1-dimethylethyl)-: ACTIVE
Computed Properties
Molecular Weight:357.9
XLogP3:6.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:357.1607901
Monoisotopic Mass:357.1607901
Topological Polar Surface Area:50.9
Heavy Atom Count:25
Complexity:473
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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