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Benzyl benzoate, Benzyl phenylformate, Benzyl alcohol benzoic ester,  Ascabin, Benylate, Ascabiol, Scabagen, Vanzoate, Benzyl ester, 120-51-4 

Benzyl benzoateBenzyl phenylformateBenzyl alcohol benzoic ester,  AscabinBenylateAscabiolScabagenVanzoateBenzyl ester, 120-51-4 

CAS: 120-51-4

Molecular Formula: C14H12O2

Names and Identifiers

Name Benzyl benzoate
Synonyms Ascabin
Benylate
Ascabiol
Scabagen
Vanzoate
VANZOATE(R)
Benzyl ester
VENZONATE(R)
Benzyl benzoate
Benzyl benzoate BP
BENZOATO DE BENCILO
Benzyl phenylformate
Phenylmethyl benzoate
Benzoic acid benzyl ester
Benzyl benzene carboxylate
Benzyl alcohol benzoic ester
Benzoic acid phenylmethyl ester
CAS 120-51-4
EINECS 204-402-9
InChI InChI=1/C14H12O2/c15-14(13-9-5-2-6-10-13)16-11-12-7-3-1-4-8-12/h1-10H,11H2
InChIKey SESFRYSPDFLNCH-UHFFFAOYSA-N

120-51-4 - Physico-chemical Properties

Molecular Formula C14H12O2
Molar Mass 212.24
Density 1.118 g/mL at 20 °C (lit.)
Melting Point 17-20 °C (lit.)
Boling Point 323-324 °C (lit.)
Flash Point 298°F
JECFA Number 24
Water Solubility practically insoluble
Solubility Miscible with ethanol, alcohol, chloroform, ether, oils
Vapor Presure 1 mm Hg ( 125 °C)
Appearance Transparent liquid
Color Clear colorless
Merck 14,1127
BRN 2049280
Storage Condition 2-8°C
Stability Stable. Substances to be avoided include strong oxidizing agents. Combustible.
Sensitive Sensitive to light
Refractive Index n20/D 1.568(lit.)
MDL MFCD00003075
Physical and Chemical Properties Character white oily liquid, slightly viscous, pure product is flake crystal. There is a weak plum, almond aroma.
melting point 21 ℃
boiling point 323~324 ℃
relative density 1.1121
refractive index 1.5690
flash point 148 ℃
solubility-insoluble in water and glycerol, soluble in most organic solvents.
Use It is used for fixative of solvent and essence of Musk, substitute of camphor, also used for preparation of pertussis medicine, asthma medicine, etc

120-51-4 - Risk and Safety

Risk Codes R22 - Harmful if swallowed
R51/53 - Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. 
Safety Description S25 - Avoid contact with eyes.
S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. 
S46 - If swallowed, seek medical advice immediately and show this container or label.
UN IDs UN 3082 9 / PGIII
WGK Germany 2
RTECS DG4200000
TSCA Yes
HS Code 29163100
Hazard Class 9
Toxicity LD50 in rats, mice, rabbits, guinea pigs (g/kg): 1.7, 1.4, 1.8, 1.0 orally (Draize)

120-51-4 - Upstream Downstream Industry

Raw Materials Benzoic acid
Benzoic acid

120-51-4 - Nature

Open Data Verified Data

colorless oily liquid with weak Balsam and almond fragrance. Soluble in ethanol, ether, chloroform and oil, almost insoluble in water and glycerol.

Last Update:2024-01-02 23:10:35

120-51-4 - Preparation Method

Open Data Verified Data

The product was obtained by transesterification of ethyl benzoate with benzyl alcohol, washed with water, layered, dried and distilled. Alternatively, it is prepared by condensation of benzaldehyde.

Last Update:2022-01-01 10:07:29

120-51-4 - Introduction

It has a slightly pleasant aromatic smell and a burning smell. Can volatilize with water vapor. It is miscible with alcohol, chloroform, ether and oil, and insoluble in water or glycerin. Low toxicity, half lethal dose (rat, oral) 1700mg/kg. It's irritating.

Last Update:2022-10-16 17:12:33

120-51-4 - Use

Open Data Verified Data

mainly used as fixative. For the preparation of strawberry, pineapple, cherry and other fruit food flavor and wine flavor, but also for Jasmine, lily of the valley, ylang ylang, gardenia, Terminus, clove and other daily flavor. The amount of gum used was 280mg/kg; 39mg/kg in candy; 33mg/kg in baked food; 45mg/kg in soft drinks; 12mg/kg in cold drinks.

Last Update:2022-01-01 10:07:30

120-51-4 - Reference Information

FEMA 2138 | BENZYL BENZOATE
LogP 4 at 20℃
NIST chemical information Information provided by: webbook.nist.gov (external link)
EPA chemical information Information provided by: ofmpub.epa.gov (external link)
freezing point the freezing point of benzyl benzoate is ≥ 17 ℃. in winter, because it condenses into a solid, when using, the benzyl benzoate package can be placed in a drying room (temperature 35-70 ℃) or warm water (temperature 40-90 ℃) water bath for use after melting.
content analysis determined by method 1 in ester content determination method (OT-18). The amount of sample taken is 1g. Equivalent factor in calculation (e)
toxicity ADI 0~5 mg/kg(FAO/WHO,1994). LD50500mg/kg (rat, oral).
usage limit FEMA(mg/kg): soft drink 4.5; Cold drink 12; Candy 39; Baked food 33; Gum sugar 280. Moderate limit (FDA § 172.515,2000).
use is a good fixer, diluent or solvent in essence, especially in flower fragrance. It can be used as a modifier in heavy floral and oriental fragrance types, tuberose, ylang ylang, lilac, gardenia and other fragrance types. It is also a stabilizer for high-carbon aldehyde or alcohol fragrances, and a good solvent for certain solid fragrances. It is also commonly used as a fixer in the formulation of edible flavors.
benzyl benzoate can be used as a solvent for cellulose acetate, perfume fixing agent, candy flavoring agent, plastic plasticizer and insect repellent. When the product is used as a spice, the product specification can refer to Shanghai Q/QBH68-79, and the ester content is above 99%. It can be used as a fixer for a variety of floral flavors, and is also the only best solvent for solid flavors that are difficult to dissolve in flavors. It can dissolve artificial musk in flavors (1kg benzyl benzoate can dissolve 0.45kg sunflower musk, 0.205kg ketone musk or 0.28kg xylene musk), and is also used to prepare whooping cough medicine, asthma medicine, etc. In addition, benzyl benzoate is also used in textile auxiliaries, scabies creams, pesticide intermediates, etc.; in textile auxiliaries, mainly used as a dye guide, leveling agent, repair agent, etc.; in polyester and compact fiber The field is widely used.
Production method Heat reaction of sodium benzyl alcohol with benzaldehyde, or reaction of sodium benzoate with benzyl chloride. Ethyl benzoate and benzyl alcohol are also used in the perfume industry.
It is formed by the co-thermal esterification of sodium benzoate and benzoyl chloride in the presence of triethylamine. Under the conditions of stirring and cooling, sodium is dissolved in benzyl alcohol, then benzaldehyde is slowly added, and the effect is completely heated in a water bath for 1~2h, the precipitated oil layer is separated, washed and fractionated. Benzyl alcohol is esterified with benzoic acid. It is obtained by transesterification and fractionation of benzoate with benzyl alcohol using sodium carbonate as a catalyst. Br> benzyl benzoate naturally exists in Peruvian balsam, tuberose, carnation and tulu balsam, etc. It is usually produced by chemical synthesis in industry. 7g(0.07 mo1) benzyl alcohol was added to a 100mL round bottom flask, 0.3g(0.013mol) of sodium metal was added to dissolve in it within 30min, and after cooling to room temperature, it was slowly added into a 250mL three-mouth bottle containing 45.4g(0.43 mo1) benzaldehyde. The mixture heats up due to the reaction and is cooled with water so that the temperature does not exceed 50~60 ℃. After about 30min, when the temperature stopped rising, heating in the water bath to continue the reaction for 1h. After the reactants are cooled, use 40mI. Wash with water twice. The obtained oil is distilled under reduced pressure. Benzyl alcohol, unreacted benzaldehyde and a small amount of water are first distilled, and then a fraction of 184~185 ℃(2kPa) is collected to obtain about 40g of product. 2C6H5CHO→ C6H5COOCH2C6H5 benzyl alcohol and ethyl benzoate are transesterified in the presence of sodium carbonate. After the reaction is over, the ethanol is removed by atmospheric distillation, and then the benzyl alcohol is removed by vacuum distillation. After cooling, the product is washed, layered, dried, and finally distilled under reduced pressure. C6H5COOCH2CH3 C6H5CH2OH[Na2CO3]→C6H5COOCH2C6H5 CH3CH2OH
category pesticide
toxicity classification poisoning
acute toxicity oral-rat LD50:1700 mg/kg; Oral-mouse LD50: 1400 mg/kg
Explosive hazard characteristics Intense reaction with oxidant
flammability hazard characteristics more flammable liquid; combustion produces stimulating smoke
storage and transportation characteristics ventilation and low temperature drying; storage with oxidant
fire extinguishing agent dry powder, carbon dioxide, mist water
auto-ignition temperature 896 °F

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