B6630
Benzyl benzoate
≥99.0%, liquid, ReagentPlus®
동의어(들):
Benzoic acid benzyl ester
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
C6H5COOCH2C6H5
CAS 번호:
Molecular Weight:
212.24
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
204-402-9
MDL number:
Beilstein/REAXYS Number:
2049280
제품 이름
Benzyl benzoate, ReagentPlus®, ≥99.0%
InChI key
SESFRYSPDFLNCH-UHFFFAOYSA-N
InChI
1S/C14H12O2/c15-14(13-9-5-2-6-10-13)16-11-12-7-3-1-4-8-12/h1-10H,11H2
SMILES string
O=C(OCc1ccccc1)c2ccccc2
vapor pressure
1 mmHg ( 125 °C)
product line
ReagentPlus®
assay
≥99.0%
form
liquid
autoignition temp.
896 °F
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.)
functional group
ester
phenyl
Quality Level
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Application
Benzyl benzoate has been used to:
- Prepare benzyl alcohol/benzyl benzoate (BABB) solution employed for enhancing the tissue transparency during the whole-mount immunostaining BABB method.
- Study its ability to induce an olfactory response in the third instar larvae of Drosophila melanogaster.
- Prepare Spalteholz fluid in combination with methyl salicylate, employed during LSFM (light sheet fluorescence microscopy) imaging.
General description
Benzyl benzoate is a benzyl compound that can be synthesized by reacting benzyl chloride with sodium benzoate in the presence of tetrabutylaramonium iodide. It is reported to be the key constituent in the essential oils isolated from leaves and stem bark of Cinnamomum zeylanicum. Its toxicity has been assessed. The mechanism of thermal decomposition of benzyl benzoate has been investigated.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2
저장 등급
10 - Combustible liquids
wgk
WGK 2
flash_point_f
298.4 °F - closed cup
flash_point_c
148 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Toxicity studies on benzyl benzoate and related benzyl compounds.
B E GRAHAM et al.
The Journal of pharmacology and experimental therapeutics, 84, 358-362 (1945-08-01)
Benzyl benzoate, the major component of the leaf and stem bark oil of Cinnamomum zeylanicum Blume.
Nath SC, et al.
J. Essent. Oil Res., 8(3), 327-328 (1996)
Kinetics of phase transfer catalytic preparation of benzyl benzoate.
Chang JR, et al.
J. Chin. Chem. Soc., 31(2), 185-190 (1984)
Jos van Rooij et al.
Biomedical optics express, 10(4), 1782-1793 (2019-05-16)
In this work we demonstrate large-scale high-sensitivity optical diffraction tomography (ODT) of zebrafish. We make this possible by three improvements. First, we obtain a large field of view while still maintaining a high resolution by using a high magnification over
Pyrolytic Chemistry of Benzyl Benzoate.
Chen PS and Chou CH.
J. Chin. Chem. Soc., 41(5), 597-599 (1994)
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