Ultraviolet absorber UV-326 CAS#:3896-11-5; 凯望编码 (ChemWhat Code): 50770

IdentificationPhysical DataSpectra
Route of Synthesis (ROS)Safety and HazardsOther Data

Identification

Product NameUltraviolet absorber UV-326
IUPAC Name2-tert-butyl-6-(5-chlorobenzotriazol-2-yl)-4-methylphenoll
Molecular StructureStructure of Ultraviolet absorber UV-326 CAS 3896-11-5
CAS Registry Number 3896-11-5
EINECS Number223-445-4
MDL NumberMFCD00059707
Beilstein Registry NumberNo data available
Synonyms2-(3-tert-butyl-2-hydroxy-5-methylphenyl)-2H-5-chlorobenzotriazole
Molecular FormulaC17H18ClN3O
Molecular Weight315.797
InChIInChI=1S/C17H18ClN3O/c1-10-7-12(17(2,3)4)16(22)15(8-10)21-19-13-6-5-11(18)9-14(13)20-21/h5-9,22H,1-4H3
InChI KeyOCWYEMOEOGEQAN-UHFFFAOYSA-N
Canonical SMILESCc1cc(c(c(c1)n2nc3ccc(cc3n2)Cl)O)C(C)(C)C
Patent Information
Patent IDTitlePublication Date
US2020/325107BENZOTRIAZOLE COMPOUND2020
US2019/107647OPTICAL MATERIAL COMPRISING A RED-SHIFTED BENZOTRIAZOLE UV ABSORBER2019
CN108148009A transfer method using catalytic preparation of benzo triazole ultraviolet ray absorbing agent (by machine translation)2018
WO2013/188490STABILIZER COMPOSITIONS CONTAINING SUBSTITUTED CHROMAN COMPOUNDS AND METHODS OF USE2013

Physical Data

AppearanceLight yellow powder
SolubilityNo data available
Flash PointNo data available
Refractive indexNo data available
SensitivityNo data available
Melting Point, °C Solvent (Melting Point)
140 – 141
140 – 141ethanol, CH2Cl2
139 – 141
141.5 – 142

Spectra

Description (NMR Spectroscopy)Nucleus (NMR Spectroscopy)Solvents (NMR Spectroscopy)Comment (NMR Spectroscopy)
Chemical shifts, Spectrum1Hchloroform-d1
Chemical shifts13Cchloroform-d1
Chemical shifts13Cneat (no solvent, solid phase)
Chemical shifts15Nneat (no solvent, solid phase)
Chemical shifts, Spectrum15Nchloroform-d1
HMBC (Heteronuclear Multiple Bond Coherence), Spectrum1H,15Nchloroform-d1
Description (IR Spectroscopy)Comment (IR Spectroscopy)
Bands3080 cm**(-1)
IR
Description (Mass Spectrometry)
liquid chromatography mass spectrometry (LCMS), tandem mass spectrometry, spectrum
spectrum
negative ion spectroscopy
Description (UV/VIS Spectroscopy)Solvent (UV/VIS Spectroscopy)Absorption Maxima (UV/VIS), nm
Spectrumdichloromethane
Spectrumchloroform353
Spectrumchloroform353
Spectrum353.5

Route of Synthesis (ROS)

Route of Synthesis (ROS) of Ultraviolet absorber UV-326 CAS 3896-11-5
Route of Synthesis (ROS) of Ultraviolet absorber UV-326 CAS 3896-11-5
ConditionsYield
With platinum on activated charcoal; hydrogen at 50 – 75℃; under 3750.38 – 6000.6 Torr; Autoclave;

Experimental Procedure
Step 3: The intermediate nitrogen oxide solution of formula II obtained in step 2 is transferred to an autoclave, Pt / C catalyst is introduced and hydrogen gas is introduced; the reaction temperature is controlled at 50-65 DEG C and the hydrogen pressure is adjusted to 0.5 to 0.8 MPa (constant), when the hydrogen absorption amount is lower than 0.05MPa / min, and the temperature is raised to 75 DEG C for 0.5 to 3 hours, the hydrogen reduction reaction is completed; Step 4: The mixed solution obtained in Step 3 is filtered to remove the catalyst,Reducing the temperature of the reducing liquid to 5-10 DEG C to precipitate the solid, separating the aqueous phase and adjusting the pH to 8.5-9.5,Precipitating a solid; combining the two solids to give a crude product of the trisazolyl type ultraviolet absorber of formula III;Step 5: A portion of the second solvent was added to the crude product obtained in Step 4,Heating to 50 to 75 DEG C and holding for 0.5 to 2 hours,Keeping and slowly adding the remaining second solvent to the system near the dissolution or just clear (visual),The filtrate was cooled to 0 to 10 ° C after hot filtration, and the precipitated solid was collected,To obtain a benzotriazole-based light stabilizer of high purity as shown in Formula III;
92.1%

Safety and Hazards

GHS Hazard StatementsH413 (88.99%): May cause long lasting harmful effects to aquatic life [Hazardous to the aquatic environment, long-term hazard]
Information may vary between notifications depending on impurities, additives, and other factors.
Precautionary Statement CodesP273, and P501
(The corresponding statement to each P-code can be found at the GHS Classification page.)

Other Data

TransportationNONH for all modes of transport
Under the room temperature and away from light
HS CodeNo data available
StorageUnder the room temperature and away from light
Shelf Life2 years
Market PriceUSD
Druglikeness
Lipinski rules component
Molecular Weight315.802
logP6.455
HBA3
HBD1
Matching Lipinski Rules3
Veber rules component
Polar Surface Area (PSA)50.94
Rotatable Bond (RotB)2
Matching Veber Rules2
Use Pattern
Ultraviolet absorber UV-326 CAS#:3896-11-5 Environmental protection
Ultraviolet absorber UV-326 CAS#:3896-11-5 UV absorber
Ultraviolet absorber UV-326 CAS#:3896-11-5 UVA (ultraviolet absorber)
Ultraviolet absorber UV-326 CAS#:3896-11-5 ultraviolet ray absorbing agent
UV absorber for dye liquor
precipitating additive for antimicrobial thermoplastic elastomer compositions
useful as UV absorbing and light stabilizing additive in plastic films and fibers

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