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Xiamen ShengLang SaiChuang Biological Technology Co., Ltd
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​benzyl benzoate
​benzyl benzoate
Supply Ability:
100 Kilogram/Kilograms per Month
Port:
shenzhen
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Kilogram
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Place of Origin:
China
Brand Name:
yc
Model Number:
Packaging & Delivery
Product Description

Product name 

benzyl benzoate 


Molecular formula C14H12O2 

Molecular weight 212.24 

Melting point 17 oC 



Alias: Benzoic acid benzyl ester 

Purity : 99% 

CAS Registry Number: 120-51-4 

Einecs No: 204-402-9 

Type: Synthetic Flavour & Fragrance 

Storage: in dry cool place,keep container closed tightly,well ventilated. 

Lead time :within 24 hours upon receipt of payment 

Delivery time : 4-6 working days by Air for quantity less than 200kgs 

Appearance:colorless to pale yellow transparent liquid 


Description:


 


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.


Usage: 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.


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