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UV Absorber 326

Characterization Physical Properties Features/Benefits Applications Guidelines for use Handling & Safety

UV Absorber 326

CAS No.3896-11-5
Chemical Name:UV Absorber 326
CBNumber:CB4256124
Molecular Formula:C17H18ClN3O
Formula Weight:315.8
MOL File:3896-11-5.mol

UV Absorber 326 Property

Melting point 144-147 °C(lit.)
Boiling point 460.4±55.0 °C(Predicted)
Density 1.26±0.1 g/cm3(Predicted)
vapor pressure 0Pa at 20℃
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form Solid
pka 9.31±0.48(Predicted)
color Pale Yellow to Light Yellow
Water Solubility 4μg/L at 20℃
InChI InChI=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
InChIKey OCWYEMOEOGEQAN-UHFFFAOYSA-N
SMILES C1(O)=C(C(C)(C)C)C=C(C)C=C1N1N=C2C=C(Cl)C=CC2=N1
LogP 6.580 (est)
Indirect Additives used in Food Contact Substances 2-(3'-TERT-BUTYL-2'-HYDROXY-5'-METHYL-PHENYL)-5-CHLOROBENZOTRIAZOLE
CAS DataBase Reference 3896-11-5(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 7ZF18Q354W
EPA Substance Registry System 2-tert-Butyl-6-(5-chloro-2H-benzotriazol-2-yl)-p-cresol (3896-11-5)
UNSPSC Code 12162002
NACRES NA.23

Safety

Hazard Codes :Xi
Risk Statements :36/37/38-53
Safety Statements :26-36-61
WGK Germany :1
HS Code :29339900

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal wordWarning
Hazard statements H315-H319
Precautionary statements P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313

UV Absorber 326 Price More Price(3)

Brand: Sigma-Aldrich(India)
Product number: 422479
Product name : 2-tert-Butyl-6-(5-chloro-2H-benzotriazol-2-yl)-4-methylphenol
Purity: 98%
Packaging: 50G
Price: ₹5423.33
Updated: 2022/06/14
Buy: Buy

Brand: TCI Chemicals (India)
Product number: H0559
Product name : 2-(5-Chloro-2-benzotriazolyl)-6-tert-butyl-p-cresol
Purity: min. 98.0 %
Packaging: 25G
Price: ₹2900
Updated: 2022/05/26
Buy: Buy

Brand: TCI Chemicals (India)
Product number: H0559
Product name : 2-(5-Chloro-2-benzotriazolyl)-6-tert-butyl-p-cresol
Purity: min. 98.0 %
Packaging: 500G
Price: ₹8100
Updated: 2022/05/26
Buy: Buy

UV Absorber 326 Chemical Properties,Usage,Production

Characterization UV Absorber 326 is a UV absorber of the hydroxyphenylbenzotriazole class, which imparts outstanding light stability to plastics and other organic substrates.
Physical Properties
Features/Benefits UV Absorber 326 has a wide range of indirect food approvals in polyolefins. It has a low volatility at high temperatures and high resistance to thermal degradation and can therefore be used without significant loss or decomposition in the polyolefin compounding and molding processes. In the use for the UV protection of polyester resins, TINUVIN 326 does not form colored complexes with the metallic salts used for the curing process of these resins.
Applications UV Absorber 326 is especially suited for polyolefins and cold cured polyesters.
Guidelines for use
Handling & Safety In accordance with good industrial practice, handle with care and avoid unnecessary personal contact. Avoid continuous or repetitive breathing of dust. Use only with adequate ventilation. Prevent contamination of the environment. Avoid dust formation and ignition sources. For more detailed information please refer to the material safety data sheet.
Chemical Properties Pale Yellow Solid
Originator Bumetrizole,Onbio Inc.
Uses Bumetrizole is an intermediate reactant in the synthesis of UV light absorbers for polyester fibers.
Uses UV-326 can potentially be used as a UV light filter in cosmetics and sunscreens. It may also be used as a corrosion inhibitor for the protection of building materials and automobiles.
Manufacturing Process To a 2000 ml 3-necked, round-bottomed flask equipped with an agitator, reflux condenser, nitrogen inlet and thermometer were charged 140.5 g of 2'- hydroxy-3'-t-butyl-5'-methyl-5-chloro-2-nitroazobenzene, 119 g of isopropanol and 80 g of Amsco mineral spirits. A stream of nitrogen was introduced over the surface of the contents of the flask and the nitrogen atmosphere was then maintained throughout the remainder of the reduction process. 13.7 g of 50% aqueous sodium hydroxide solution and 222 g of water were added and the temperature of the contents of the flask were adjusted to 55°C. The ratio of the moles of alkali to moles of o-nitroazobenzene intermediate used was is 0.848/1. 104 g of zinc dust was added in 5 portions over a 2 hours period with the temperature of the flask being held at 55-60°C with some slight external cooling. The total concentration of iron impurities from all reactants less than 150 ppm based on zinc used. After all the zinc was added, the temperature was raised to 60°C and held at this temperature until a spot test indicated no more o-nitroazobenzene intermediate was present. The temperature was then raised to 65°C and held there for 4 to 5 hours or until TLC analysis indicated that no more of the N-oxy-intermediate was present. 62.6 g of anhydrous sodium sulfate and 35.6 g of water were then added, the batch was heated to 70°C and stirred for 15 min. The material was then allowed to stand and separate into three liquid phases plus unreacted zinc dust. The top two layers containing the desired product were transferred to another flask. The remaining aqueous zinc slurry was washed at 65-70°C with three successive 16 g portions of Amsco mineral spirits: isopropanol 50:50. The combined product layers and wash liquids were then washed once at 70°C with an aqueous hydrochloric acid solution made from 130 g of water and 40 g of 32% hydrochloric acid to remove cleavage amine by-products. A second and third wash followed at 70°C with aqueous hydrochloric acid solutions made each from 65 g of water and 20 g of 32% hydrochloric acid. The last wash was essentially colorless. 14 g of 32% hydrochloric acid and 220 g of isopropanol were added to the solution of the product. The batch was allowed to crystallize slowly. The solid product form was filtered and washed with isopropanol at 0°C to give 110 g of 5-chloro-2-(2-hydroxy-3-t-butyl-5- methylphenyl)-2H-benzotriazole with a melting point of 140-141°C.
Therapeutic Function Sunscreen agent
General Description 2-tert-Butyl-6-(5-chloro-2H-benzotriazol-2-yl)-4-methylphenol (UV-326) is a benzotriazole based UV absorber that can be used in the photostabilization of industrial materials. It can absorb the harmful UV radiation for the wavelength of about 290 nm.
Flammability and Explosibility Not classified