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BENZOIN
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PRODUCT IDENTIFICATION |
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CAS NO. | 119-53-9 | |
EINECS NO. | 204-331-3 | |
FORMULA | C6H5CH(OH)COC6H5 | |
MOL WT. | 212.25 | |
H.S. CODE | 2914.49 | |
TOXICITY | Oral rat LD50: 10 gm/Kg | |
SYNONYMS | 2-Hydroxy-2-phenylacetophenone; | |
2-Hydroxy-1,2-Diphenylethanone; Alpha-hydroxybenzyl phenyl ketone; DL-Benzoin; | ||
SMILES |
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CLASSIFICATION |
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PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE | Off-white crystals, Slight camphor odor | |
MELTING POINT | 137 C | |
BOILING POINT | 344 C | |
SPECIFIC GRAVITY |
1.31 | |
SOLUBILITY IN WATER | 0.03 g/100ml | |
AUTOIGNITION | ||
pH | ||
VAPOR PRESSURE | 1.1 | |
NFPA RATINGS | Health: 1 Flammability: 1 Reactivity: 0 | |
FLASH POINT |
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STABILITY | Stable under ordinary conditions | |
APPLICATIONS |
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Benzoin is a highly toxic crystalline substance with formula of C6H5CH(OH)COC6H5, alpha-hydroxy aromatic ketone. It is a white to yellowish crystals; slightly soluble in water, soluble in acetone; melting at 137 C. It is prepared by the condensation of benzaldehyde in an alkaline cyanide solution. Benzoin and its derivatives are used as intermedaites for the synthesis of organic compounds and as catalysts in photopolymerization. They are used for anticratering in powder coatings. | ||
SALES SPECIFICATION | ||
APPEARANCE |
Light yellow powder | |
ASSAY |
99.5% min | |
MELTING POINT | 134 C min | |
LOSS ON DRYING |
0.5% max | |
TRANSPORTATION | ||
PACKING | 25kgs in Bag | |
HAZARD CLASS | ||
UN NO. | ||
GENERAL DESCRIPTION OF PHOTOINITIATOR | ||
Polymerization is initiated generally by free radical. There are four types of
free radical initiators which initiate polymerization.
The main advantage of polymerization started by photoinitiators is temperature-independence and easy control. It can be conducted at very low temperatures and can be stopped simply by removing the light source. Photoinitiators are compounds that break down into free radicals upon exposure to ultraviolet radiation. Photoinitiators undergo a unimolecular bond cleavage upon irradiation to yield free radicals (benzoin esters; benzil ketals; alpha-dialkoxy acetophenones; alpha-hydroxy-alkylphenones; alpha-amino alkyl- phosphine; acylphosphine oxides). Another type of photoinitiators undergo a bimolecular reaction where the excited state of the photoinitiator interacts with a second molecule (a coinitiator) to generate free radicals(benzo phenones,amines; thioxanthones,amines; titanocenes). Photoinitiators are widely applied in UV curing inks, wood coatings, paper coatings, optical fiber, PCB, screen printing , paper varnish and other surface coatings. |
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