推荐产品
蒸汽密度
3 (20 °C, vs air)
品質等級
蒸汽壓力
73 mmHg ( 20 °C)
產品線
ReagentPlus®
化驗
≥99.8%
形狀
liquid
自燃溫度
801 °F
expl. lim.
2.2-11.5 %, 38 °F
雜質
≤0.003 mg/mL non-volatile matter
≤0.02% Ethyl alcohol
≤0.05% water
折射率
n20/D 1.3720 (lit.)
bp
76.5-77.5 °C (lit.)
mp
−84 °C (lit.)
溶解度
alcohol: soluble(lit.)
chloroform: soluble(lit.)
water: soluble
密度
0.902 g/mL at 25 °C (lit.)
格式
neat
SMILES 字串
CCOC(C)=O
InChI
1S/C4H8O2/c1-3-6-4(2)5/h3H2,1-2H3
InChI 密鑰
XEKOWRVHYACXOJ-UHFFFAOYSA-N
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一般說明
Ethyl acetate, a carboxylate ester, is bio-friendly organic solvent with wide range of industrial applications. Its synthesis by reactive distillation and by acceptorless dehydrogenative dimerization of ethanol has been explored. Its utility as a less toxic alternative to diethyl ether in the formalin-ether (F-E) sedimentation procedure for intestinal parasites has been investigated. 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.
應用
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 multi-residue analysis of pesticide residues in fruit and vegetables.
- Acetylation of primary amines to form amides in the presence of dimethyltin(IV) acetic acid distannoxane.
Meets urethane grade requirements (H2O ≤ 0.05%)
法律資訊
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
訊號詞
Danger
危險聲明
危險分類
Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
標靶器官
Central nervous system
安全危害
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 1
閃點（°F）
24.8 °F - closed cup
閃點（°C）
-4 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
Christer Jansson et al.
Journal of chromatography. A, 1023(1), 93-104 (2004-02-06)
A new multi-residue method for determination of pesticide residues in a wide variety of fruit and vegetables, using the National Food Administration (NFA) ethyl acetate extraction and determination by means of LC-MS/MS, is presented. The method includes pesticides normally detected
Perspectives for the biotechnological production of ethyl acetate by yeasts.
Loser C, et al.
Applied Microbiology and Biotechnology, 98(12), 5397-5415 (2014)
Anatase thin films on glass from the chemical vapor deposition of titanium (IV) chloride and ethyl acetate.
O'Neill SA, et al.
Chemistry of Materials, 15(1), 46-50 (2003)
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)
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