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Merck

650528

Ethyl acetate

HPLC Plus, for HPLC, GC, and residue analysis, 99.9%

동의어(들):

EtOAc

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제품정보 (DICE 배송 시 비용 별도)

Linear Formula:
CH3COOC2H5
CAS 번호:
141-78-6
Molecular Weight:
88.11
UNSPSC Code:
12190000
NACRES:
NA.21
PubChem Substance ID:
329760026
EC Number:
205-500-4
Beilstein/REAXYS Number:
506104
MDL number:
MFCD00009171
Assay:
99.9%
Grade:
HPLC Plus
Technique(s):
HPLC: suitable, gas chromatography (GC): suitable
Bp:
76.5-77.5 °C (lit.)
Vapor pressure:
73 mmHg ( 20 °C)

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grade

HPLC Plus

Quality Level

100

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

99.9%

form

liquid

autoignition temp.

801 °F

expl. lim.

2.2-11.5 %, 38 °F

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

impurities

≤0.03% water, ≤1.0 ppb Fluorescence (quinine) at 365 nm, ≤10 ng/L Pesticide residue analysis (as heptachlor epoxide)

evapn. residue

≤0.0001%

refractive index

n20/D 1.3720 (lit.)

bp

76.5-77.5 °C (lit.)

mp

−84 °C (lit.)

solubility

alcohol: soluble(lit.), chloroform: soluble(lit.)

density

0.902 g/mL at 25 °C (lit.)

λ

H2O reference

UV absorption

λ: 256 nm Amax: ≤1.00, λ: 275 nm Amax: ≤0.05, λ: 300 nm Amax: ≤0.03, λ: 325-400 nm Amax: ≤0.005

suitability

suitable for residue analysis

application(s)

PFAS testing

format

neat

SMILES string

CCOC(C)=O

InChI

1S/C4H8O2/c1-3-6-4(2)5/h3H2,1-2H3

InChI key

XEKOWRVHYACXOJ-UHFFFAOYSA-N

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관련 카테고리

General description

Ethyl acetate (EA), 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. Its ability as an acyl acceptor in the immobilized lipase-mediated preparation of biodiesel from crude vegetable oils has been examined. The complete degradation of ethyl acetate to CO2 using manganese octahedral molecular sieve (OMS-2) has been investigated. EA is an effective alternate solvent of diethyl ether, employed for the concentration of eggs, larvae, and cysts in fecal specimens during the Formalin-ether sedimentation technique. Acetaldehyde is reaction intermediate formed during the oxidative combustion of ethanol and ethyl acetate in the presence of copper oxide embedded on Ce-doped titania surface.

Application

Suitable for HPLC, spectrophotometry, environmental testing

Packaging

M-Bottle for Solvents
As a global leader in lab reagents, we are constantly looking for new ways to optimize the safety of our products. The newly developed 4L solvent bottle design features advanced sealing technology that eliminates leaks to make the handling of solvents safer and more convenient than ever before.
See all the new features here!

Other Notes

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

target_organs

Central nervous system

supp_hazards

EUH066

저장 등급

3 - Flammable liquids

flash_point_f

24.8 °F - closed cup

flash_point_c

-4 °C - closed cup

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시험 성적서(COA)

Lot/Batch Number

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이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Maria Nikolantonaki et al.
Analytica chimica acta, 660(1-2), 102-109 (2010-01-28)
As volatile thiols are nucleophiles, they are capable of additional reactions with electrophiles. In enology, this concerns reactions between volatile or non-volatile thiols and oxidized phenolic compounds. Initial studies concerning the reactivity of volatile thiols with polyphenols showed that (+)-catechin
Lasse Saaby et al.
Phytotherapy research : PTR, 25(2), 195-201 (2010-07-16)
A previously published systematic review and a metaanalysis have concluded that the consumption of standardized rose hip powder (Rosa canina L.) can reduce pain in osteoarthritis patients. Synovial inflammation has been suggested to play an important role in the pathogenesis
Manganese oxide OMS-2 as an effective catalyst for total oxidation of ethyl acetate.
Gandhe AR, et al.
Applied Catalysis. B, Environmental, 72(1), 129-135 (2007)
Investigation of ethyl acetate reactive distillation process.
Kenig EY, et al.
Chemical Engineering Science, 56(21), 6185-6193 (2001)
Catalytic Acetylation Amines with Ethyl Acetate.
Camacho-Camacho C, et al.
Main Group Metal Chemistry, 31(1-2), 13-20 (2008)
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