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1062008

USP

Benzyl benzoate

United States Pharmacopeia (USP) Reference Standard

Synonym(s):

Benzoic acid benzyl ester

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About This Item

Linear Formula:
C6H5COOCH2C6H5
CAS Number:
Molecular Weight:
212.24
Beilstein:
2049280
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

pharmaceutical primary standard

vapor pressure

1 mmHg ( 125 °C)

API family

benzyl benzoate

autoignition temp.

896 °F

manufacturer/tradename

USP

availability

not available in (Sales restrictions may apply - USP Product)

refractive index

n20/D 1.568 (lit.)

bp

323-324 °C (lit.)

mp

17-20 °C (lit.)

density

1.118 g/mL at 20 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

SMILES string

O=C(OCc1ccccc1)c2ccccc2

InChI

1S/C14H12O2/c15-14(13-9-5-2-6-10-13)16-11-12-7-3-1-4-8-12/h1-10H,11H2

InChI key

SESFRYSPDFLNCH-UHFFFAOYSA-N

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General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Application


  • Topical treatment for scabies: A randomized study compared the efficacy of topical benzyl benzoate versus oral ivermectin for treating scabies, highlighting its potential as an effective treatment option for this parasitic infestation (Meyersburg et al., 2023).

  • Repellency against Tribolium castaneum: Research on benzyl benzoate demonstrated its toxicity and repellency efficacy, offering an eco-friendly alternative for controlling the red flour beetle Tribolium castaneum, which poses a significant threat to stored agricultural products (Aboelhadid et al., 2023).

Analysis Note

These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.  ​

Other Notes

Sales restrictions may apply.

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Pictograms

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Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

298.4 °F - closed cup

Flash Point(C)

148 °C - closed cup


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Catherine W McCollum et al.
Aquatic toxicology (Amsterdam, Netherlands), 152, 152-163 (2014-04-29)
Exposure to arsenic in its inorganic form, arsenite, causes adverse effects to many different organs and tissues. Here, we have investigated arsenite-induced adverse effects on vascular tissues in the model organism zebrafish, Danio rerio. Zebrafish embryos were exposed to arsenite
Xiaonan Yan et al.
The Journal of endocrinology, 222(1), 73-85 (2014-05-16)
In adolescent girls with polycystic ovary syndrome (PCOS), neuroendocrine derangements manifest after the onset of puberty, characterized by rapid LH pulse frequency. The early mechanism underlying the pubertal regulation of the GNRH/LH pulsatile release in adolescents with PCOS remains uncertain.
Mervyn L Elgart
Expert opinion on pharmacotherapy, 4(9), 1521-1524 (2003-08-29)
In the US, 6% sulfur in petrolatum has been the most frequently administered treatment for infantile scabies. It appears to be safe but there is no literature containing a large series of patients on which to base that determination. In
Haribalan Perumalsamy et al.
Journal of medical entomology, 51(3), 650-657 (2014-06-06)
Pyroglyphid house dust mites are the most common cause of allergic symptoms in humans. An assessment was made of the toxicity of basil, Ocimum basilicum L, essential oil, 11 basil oil constituents, seven structurally related compounds, and another 22 previously
Sandrine Joly et al.
The European journal of neuroscience, 40(7), 3021-3031 (2014-07-22)
The lack of axonal regeneration in the adult central nervous system is in part attributable to the presence of inhibitory molecules present in the environment of injured axons such as the myelin-associated proteins Nogo-A and MAG and the repulsive guidance

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