UV Absorber 326

UV Absorber 326 price More Price(3)

Manufacturer	Product number	Product description	CAS number	Packaging	Price	Updated	Buy
Sigma-Aldrich	422479	2-tert-Butyl-6-(5-chloro-2H-benzotriazol-2-yl)-4-methylphenol 98%	3896-11-5	50g	$60.7	2020-08-18	Buy
TCI Chemical	H0559	2-(5-Chloro-2-benzotriazolyl)-6-tert-butyl-p-cresol >98.0%(GC)	3896-11-5	25g	$60	2020-06-24	Buy
TCI Chemical	H0559	2-(5-Chloro-2-benzotriazolyl)-6-tert-butyl-p-cresol >98.0%(GC)	3896-11-5	500g	$189	2020-06-24	Buy

UV Absorber 326 Chemical Properties,Uses,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.

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

UV Absorber 326 Preparation Products And Raw materials

Raw materials

Preparation Products

UV Absorber 326 Suppliers

Supplier	Tel	Fax	Email	Country	ProdList	Advantage
QINGDAO JADE NEW MATERIAL TECNOLOGY CO.,LTD	+86 13658692156	（+86-532）68077006	zandrew@jadenmtc.com	CHINA	219	58
RIANLON CORPORATION	+(86)13011086067 +86 18522174966	+86 22 8371 8815	market@rianlon.com	CHINA	88	58
Henan DaKen Chemical CO.,LTD.	+86-371-55531817		info@dakenchem.com	CHINA	21842	58
Shanghai Bojing Chemical Co.,Ltd.	+86-21-37122233	+86-21-37127788	Candy@bj-chem.com	CHINA	497	55
Henan Tianfu Chemical Co.,Ltd.	0371-55170693	0371-55170693	info@tianfuchem.com	CHINA	22625	55
Shanghai Time Chemicals CO., Ltd.	+86-021-57951555	+86-021-57951555	jack.li@time-chemicals.com	CHINA	1365	55
Hangzhou FandaChem Co.,Ltd.	0086 158 5814 5714 (Mobile	+86-571-56059825	fandachem@gmail.com	CHINA	3274	55
Hefei TNJ Chemical Industry Co.,Ltd.	86-0551-65418684 18949823763	86-0551-65418684	info@tnjchem.com	China	2754	55
Tianjin Zhongxin Chemtech Co., Ltd.	022-66880623	022-66880086	sales@tjzxchem.com	CHINA	602	58
career henan chemical co	+86-371-86658258		sales@coreychem.com	CHINA	30039	58

3896-11-5(UV Absorber 326)Related Search:

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• UV ABSORBER 326
• Ultraviolet absorber UV-326 Bumetrizole
• Phenol, 2-(5-chloro-2H-benzotriazol-2-yl)-6-(1,1-dimethylethyl)-4-methyl-
• ACETOSTAB 326
• ULTRA-VIOLET ABSORBER UV-326
• ULTRAVIOLET ABSORBENT UV-326
• 2-(5-chloro-2h-benzotriazol-2-yl)-6-(1,1-dimethylethyl)-4-methyl-pheno
• 2-T-BUTYL-6-(5-CHLORO-2 H-BENZOTRIAZOL-2-YL)-4-METHYLPHENOL
• BUMETRIZOLE
• LABOTEST-BB LT00138024
• TINUVIN 326
• Tinuvin 326 Ciba
• 2-(5-Chloro-2H-benzotriazole-2-yl)-4-methyl-6-(tert-butyl)phenol
• 5-Chloro-2-[3-(tert-butyl)-2-hydroxy-5-methylphenyl]-2H-benzotriazole
• Sumisorb 300
• 2(2’-Hydroxy-3’-t-butyl-5’-methylphenyl-5-chlorobenzotriazol
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• 2-tert-butyl-6-(5-chlorobenzotriazol-2-yl)-4-methyl-phenol
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• 2-(tert-Butyl)-6-(5-chloro-2H-benzo[d][1,2,3]triazol-2-yl)-4-Methylphenol
• 2-tert-Butyl-6-(5-chloro-2H-benzotriazol-2-yl)-4-Methylphenol 98%
• 2-(5-Chloro-2-benzotriazolyl)-6-tert-butyl-p-cresol
• HRsorb-326
• 2-(2'-Hydroxy-3'-tert-butyl-5'-methylphenyl)-5-chlorobenzortriazole
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• 2-(5-chloro-2h-benzotriazol-2-yl)-6
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• 2-tert-butyl-6-(5-chloro-2H-1,2,3-benzotriazol-2-yl)-4-methylphenol
• 2-(5-Chloro-2H-benzotriazol-2-yl)-6-tert-butyl-p-cresol (OH=1)
• 2-tert-butyl-6-(5-chloro-2h-benzotriazol-2-yl)-4-
• tinuvin
• 2-(3-tert-butyl-2-hydroxy-5-methylphenyl)-5-chlorobenzotriazole
• 6-tert-butyl-2-(5-chlorobenzotriazol-2-yl)-p-cresol
• UV-326
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• UV ABSORBER UV-326
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• 2-(2-HYDROXY-3-TERT-BUTYL-5-METHYLPHENYL)-5-CHLOROBENZOTRIAZOLE
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• 2-(3-tert-Butyl-2-hydroxy-5-methylphenyl)-5-chloro-2H-benzotriazole
• 2-(5-TERT-BUTYL-6-HYDROXY-M-TOLYL)-5-CHLOROBENZOTRIAZOLE
• 2-(5-CHLORO-2-BENZOTRIAZOLYL)-6-TERT-BUTYL-P-CRESOL
• 2-(5-chloro-2h-benzotriazol-2-yl)-6-(1,1-dimethylethyl)-4-methylphenol
• 2-TERT-BUTYL-6-(5-CHLORO-2 H-BENZOTRIAZOL-2-YL)-4-METHYLPHENOL
• 2-tert-butyl-6-(5-chloro-2-benzotriazolyl)-4-methylphenol
• Bumetrizole UV-326 3896-11-5
• Absorber UV-326
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• 2-(5-Chlor-2H-benzotriazol-2-yl)-6-(1,1-dimethylethyl)-4-methyl-phenol
• 2-(5-Chloro-2-benzotriazolyl)-6-tert-butyl-p-cresol>
• 2-tert-Butyl-6(5-chloro-2H-benzotriazol-2-yl)-4-methylphenol @1000 μg/mL in Acetonitrile
• 3896-11-5
• 3869-11-5
• C17H18N3OCl
• C17H18ClN3O