High Purity Benzyl Benzoate with Competitive Price (120-51-4)
|Purchase Qty. (kg)||FOB Price|
|1-999||US $1 / /|
|1,000+||US $1 / /|
Benzyl benzoate Synonyms: Benzoic acid benzyl ester; Ascabin; Ascabiol; Benylate; Benzyl alcohol benzoic ester; BENZOATO DE BENCILO; Benzoic acid phenylmethyl ester; Benzyl benzene carboxylate; Benzyl phenylformate; Phenylmethyl benzoate; Scabagen; Vanzoate; Benzyl benzoate BP
Benzyl benzoate Assay: 99.5% 99%
Benzyl benzoate CAS No.: 120-51-4
Benzyl benzoate EINECS No.: 204-402-9
Benzyl benzoate Molecular Formula: C14H12O2
Benzyl benzoate Molecular Weight: 212.24
Benzyl benzoate Density: 1.118 g/mL at 20 º C(lit. )
Benzyl benzoate Melting point: 18 º C
Benzyl benzoate Boiling point: 323-324 º C(lit. )
Benzyl benzoate Flashing point: 298 º F
Benzyl benzoate Water Solubillity: Practically insoluble
Benzyl benzoate Appearance: Colorless Oily liquid
Benzyl benzoate Packing: 25kg/Drum
Benzyl benzoate Application: Pharmaceuticals; Fixing agents; Plasticizer
Benzyl benzoate is the organic compound with the formula C6H5CH2O2CC6H5. It is the ester of benzyl alcohol and benzoic acid. It forms either a viscous liquid or solid flakes and has a weak, sweet-balsamic odor. It occurs in a number of blossoms (e. g. tuberose, hyacinth) and is a component of Balsam of Peru and Tolu balsam.
It is on the World Health Organization's List of Essential Medicines, a list of the most important medication needed in a basic health system.
Benzyl benzoate is used as an acaricide, scabicide, and pediculicide in veterinary hospitals. It is also a repellent for chiggers, ticks, and mosquitoes. It is an effective and inexpensive topical treatment for human scabies.It has vasodilating and spasmolytic effects and is present in many asthma and whooping cough drugs.
Other uses of benzyl benzoate are dye carrier, solvent for cellulose derivatives, plasticizer, and fixative in the perfume industry.
Production: Benzyl benzoate is produced industrially by the reaction of sodium benzoate with benzyl alcohol in the presence of a base. Alternatively, it is produced by transesterification of methylbenzoate and benzyl alcohol. It is also a byproduct of benzoic acid synthesis by toluene oxidation. It can also be generated by the Tishchenko reaction of benzaldehyde, using sodium benzylate and aluminium benzylate as catalysts.
|Items of Analysis||BP2000||Perfumery Grade|
|Appearance||yellowish transparent liquid||colorless transparent liquid|
|Fragrance||_||light scent of flower|
|Acidity(ml,0.1N NaOH 2.0g)||≤0.2||≤0.2|
|Specific Gravity(20°C, kg/ m3)||1118_1122||1118_1122|
(Copper Wire Mesh)