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| Gabaryty przesyłki | SKU | Dostępność | Cena netto |
|---|
Informacje o tej pozycji
Wzór liniowy:
CH3COOC2H5
Numer CAS:
Masa cząsteczkowa:
88.11
EC Number:
205-500-4
UNSPSC Code:
12352108
PubChem Substance ID:
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)
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ACS reagent
Quality Level
vapor density
3 (20 °C, vs air)
vapor pressure
73 mmHg ( 20 °C)
product line
SAFC Hitech®
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, ≤0.2% water
evapn. residue
≤0.003%
color
APHA: ≤10
refractive index
n20/D 1.3720 (lit.)
bp
76.5-77.5 °C (lit.)
mp
−84 °C (lit.)
solubility
alcohol: soluble(lit.), chloroform: soluble in salt form(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, a carboxylate ester, is bio-friendly organic solvent with a wide range of industrial applications. Its synthesis by reactive distillation and by acceptorless dehydrogenative dimerization of ethanol has been explored.[1] Its utility as a less toxic alternative to diethyl ether in the formalin-ether (F-E) sedimentation procedure for intestinal parasites has been investigated.[2] Its ability as an acyl acceptor in the immobilized lipase-mediated preparation of biodiesel from crude vegetable oils has been examined.[3] The complete degradation of ethyl acetate to CO2 using manganese octahedral molecular sieve (OMS-2) has been investigated.
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 may be used in the following processes:
- Preparation of thin films of TiO2 (titanium dioxide) on glass.
- As an extraction medium in the multiresidue analysis of pesticide residues in fruit and vegetables.[4]
- Acetylation of primary amines to form amides in the presence of dimethyltin(IV) acetic acid distannoxane.
Legal Information
SAFC Hitech is a registered trademark of Sigma-Aldrich Co. LLC
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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
Klasa składowania
3 - Flammable liquids
wgk
WGK 1
flash_point_f
24.8 °F - closed cup
flash_point_c
-4 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
Dynamics and control of an ethyl acetate reactive distillation column.
Vora N and Daoutidis P.
Industrial & Engineering Chemistry Research, 40(3), 833-849 (2001)
Towards a green process for bulk-scale synthesis of ethyl acetate: efficient acceptorless dehydrogenation of ethanol.
Martin Nielsen et al.
Angewandte Chemie (International ed. in English), 51(23), 5711-5713 (2012-04-21)
Investigation of ethyl acetate reactive distillation process.
Kenig EY, et al.
Chemical Engineering Science, 56(21), 6185-6193 (2001)
Numer pozycji handlu globalnego
| SKU | NUMER GTIN |
|---|---|
| 437549-4X4L | 04061837566554 |
| 437549-4L | 04061837566547 |

