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2-(2H-BENZOTRIAZOL-2-YL)-4,6-DI-tert-PENTYLPHENOL | ||
PRODUCT IDENTIFICATION |
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CAS NO. |
25973-55-1 |
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EINECS NO. |
247-384-8 | |
FORMULA | C22H29N3O | |
MOL WT. |
351.49 | |
H.S. CODE | 2933.99.8090 | |
TOXICITY |
Oral rat LD50: 5000 mg/kg | |
SMILES |
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SYNONYMS | 2-(3,5-Di-tert-pentyl-2-hyroxyphenyl) benzotriazole; | |
2-(2H-Benzotriazol-2-yl)-4,6-bis(1,1-dimethylpropyl)phenol; UV Absorber 328; Tinuvin®-328; | ||
SMILES |
n1(c2c(c(cc(c2)C(CC)(C)C)C(CC)(C)C)O)nc2ccccc2n1 | |
CLASSIFICATION |
Benzotriazole, UV Absorber, Light stabilizer | |
PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE |
Slightly yellowish powder | |
MELTING POINT |
80 - 83 C | |
BOILING POINT | ||
SPECIFIC GRAVITY |
1.17 | |
SOLUBILITY IN WATER |
Insoluble (0.015 mg/l at 25 C) | |
AUTOIGNITION | ||
pKa | (Dissociation Constant at 20 C) | |
log Pow | 7.25 (Octanol-water) | |
VAPOR PRESSURE | 1.93E-10 (mmHg at 25 C) | |
HENRY'S LAW | 6.52E-13 (atm-m3/mole at 25 C) | |
OH RATE | 1.58E-11 (cm3/molecule-sec at 25 C Atmospheric ) | |
VAPOR DENSITY | ||
NFPA RATINGS | ||
REFRACTIVE INDEX |
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FLASH POINT |
229 C | |
STABILITY | Stable under ordinary conditions | |
GENERAL DESCRIPTION & EXTERNAL LINKS |
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UV Absorber 328 has phenolic benzotriazole moiety and two substrates (tert-amylphenol) present on the phenolic group at 3,5 position. Phenolic Benzotriazole structure imparts important role in polymer and coating industry as UV absorbers, Light stabilizers. UV absorbers reduce or prevent the absorption of UV light by chromophores which in an excited state can form radicals that may have damaging effects on materials or alter their properties. UV Absorber 328 provides effective light stabilization and prevents yellowing and degradation of polymers such as polyurethanes, polyvinylchloride, unsaturated polyester and styrenics. http://botkinchemie.com/ 1. Strong UV absorption, especially in the 290 nm to 350 nm range which is very damaging to organic materials, and 2. Excited states formed upon UV absorption relax to the ground state extremely rapidly (picosecond time frame) and efficiently via radiation-less processes, which imparts high efficiency and excellent photostability. Chemical classes of UV absorbers suitable for use in polyolefins include 2-hydroxybenzophenones (e.g.UVA-1), 2-(2-hydroxyphenyl)-2H-benzotriazoles (e.g. UVA-2, UVA-3), tris-aryl-o-hydroxyphenyl-striazines (e.g. UVA-4), and cyanoacrylate derivatives (e.g. UVA-5, UVA-6). Chemical structures of representative UV absorbers are given in the Appendix. For food contact applications, products that have been designated as food contact compliant in polypropylene by the US FDA include UVA-1, UVA-3, UVA-4, and UVA-6......... |
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SALES SPECIFICATION | ||
APPEARANCE |
Slightly yellowish powder | |
ASSAY | 99.0 min | |
MELTING POINT |
80 C min | |
VOLATILES |
0.5% max | |
TRANSMITTANCE |
95.0% (460nm), 97.0% (500nm) | |
TRANSPORTATION | ||
PACKING | 20kg in fiber drum | |
HAZARD CLASS | ||
UN NO. |
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OTHER INFORMATION | ||
1,2,3-Benzotriazole: Benzene ring-fused azole compounds; white to off-white crystalline powder; insoluble in water, soluble in ethanol, melting at 98.5 C. Azole is a five-membered heterocycle compound containing unsaturated bonds and Nitrogen atoms. Triazole has three nitrogens. 1,2,3-Benzotriazole (1H-benzotriazole) has -N=N- bond whereas 2H-Benzotriazole has two -C=N- bonds. Benzotriazole is a parent material to produce UV-absorbers. Benzotriazole and its derivatives are versatile intermediates involved in the production of:
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