319902
Ethyl acetate
ACS reagent, ≥99.5%
Synonym(s):
EtOAc
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About This Item
Linear Formula:
CH3COOC2H5
CAS Number:
Molecular Weight:
88.11
UNSPSC Code:
12352108
NACRES:
NA.21
PubChem Substance ID:
EC Number:
205-500-4
Beilstein/REAXYS Number:
506104
MDL number:
Assay:
≥99.5%
Grade:
ACS reagent
Bp:
76.5-77.5 °C (lit.)
Vapor pressure:
73 mmHg ( 20 °C)
grade
ACS reagent
Quality Level
agency
suitable for EPA ACB B21-02, suitable for EPA ACB B23-05b
vapor density
3 (20 °C, vs air)
vapor pressure
73 mmHg ( 20 °C)
assay
≥99.5%
form
liquid
autoignition temp.
801 °F
expl. lim.
2.2-11.5 %, 38 °F
dilution
(for analytical testing)
impurities
H2SO4, passes test (darkened), ≤0.0009 meq/g Titr. acid, ≤0.200% water
evapn. residue
≤0.0030%
color
APHA: ≤10
refractive index
n20/D 1.3720 (lit.)
bp
76.5-77.5 °C (lit.)
mp
−84 °C (lit.)
density
0.902 g/mL at 25 °C (lit.)
format
neat
SMILES string
CCOC(C)=O
InChI
1S/C4H8O2/c1-3-6-4(2)5/h3H2,1-2H3
InChI key
XEKOWRVHYACXOJ-UHFFFAOYSA-N
General description
Ethyl acetate ACS grade solvent meets or exceeds the high standards of the American Chemical Society (ACS). It is ideal for most research needs and delivers replicable, publishable results.
Ethyl acetate ACS grade solvent used in:
Ethyl acetate ACS grade solvent used in:
- Routine chemical synthesis
- Drying & purification
- Critical labware cleaning
Our premium ACS solvents are ideal for routine chemical synthesis, drying, purification, and critical labware cleaning. They meet or exceed the rigorous standards of the American Chemical Society (ACS), ensuring high-quality results for your research needs.
Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.
Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.
Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.
Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.
Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.
Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.
Application
Ethyl acetate (ACS grade) can be used as a solvent in the synthesis of 6-O-acetyl glycosides via selective acetylation of carbohydrates in the presence of a catalytic amount of sulfuric acid. 6-O-acetyl glycoside derivatives are applicable as precursors for the synthesis of complex oligosaccharides.
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signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
target_organs
Central nervous system
supp_hazards
Storage Class
3 - Flammable liquids
flash_point_f
24.8 °F - closed cup
flash_point_c
-4 °C - closed cup
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A green and regioselective acetylation of thioglycoside with ethyl acetate
Liang Pi-Hui, et al.
Tetrahedron Letters, 51(52), 6928-6931 (2010)
Elif Burcu Bali et al.
Asian Pacific journal of tropical biomedicine, 4(7), 505-514 (2014-09-04)
To investigate the in vitro antimicrobial potential of Thermopsis turcica Kit Tan, Vural & Küçüködük against periodontopathogenic bacteria, its antioxidant activity and cytotoxic effect on various cancer cell lines. In vitro antimicrobial activities of ethanol, methanol, ethyl acetate (EtAc), n-hexane
Quinn P Peterson et al.
Nature protocols, 5(2), 294-302 (2010-02-06)
This protocol describes the gram-scale solution-phase synthesis of the colorimetric caspase-3/7 substrate Ac-DEVD-pNA. The caspase enzymes are integral to cellular inflammation and apoptotic cascades, and are commonly studied by cell biologists, medicinal chemists and chemical biologists. In particular, the assessment