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Merck

91238

Supelco

二乙醚

analytical standard

别名:

乙醚, 醚

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About This Item

线性分子式:
(CH3CH2)2O
CAS号:
分子量:
74.12
Beilstein:
1696894
EC號碼:
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:
NACRES:
NA.24

等級

analytical standard

品質等級

蒸汽密度

2.6 (vs air)

蒸汽壓力

2311 hPa ( 60 °C)

化驗

≥99.9% (GC)

自燃溫度

320 °F

儲存期限

limited shelf life, expiry date on the label

包含

~0.0005% 2,6-di-tert.-butyl-4-methylphenol as stabilizer

expl. lim.

36.5 %

技術

HPLC: suitable
gas chromatography (GC): suitable

雜質

≤0.1% water
water

折射率

n20/D 1.3530 (lit.)
n20/D 1.353

bp

34.6 °C (lit.)

mp

−116 °C (lit.)

密度

0.706 g/mL at 25 °C (lit.)

應用

environmental

格式

neat

SMILES 字串

CCOCC

InChI

1S/C4H10O/c1-3-5-4-2/h3-4H2,1-2H3

InChI 密鑰

RTZKZFJDLAIYFH-UHFFFAOYSA-N

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一般說明

Diethyl ether is a colorless and highly volatile organic compound, which commonly finds applications as an extraction solvent.

應用

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

推薦產品

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

象形圖

FlameExclamation mark

訊號詞

Danger

危險聲明

危險分類

Acute Tox. 4 Oral - Flam. Liq. 1 - STOT SE 3

標靶器官

Respiratory 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)

-40.0 °F - closed cup

閃點(°C)

-40 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves


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分析证书(COA)

Lot/Batch Number

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其他客户在看

Macroscale and Microscale Organic Experiments (2016)
Diethyl Ether: Organic Compound, Flammable Liquid, Boiling Point, Solvent, Ether, General Anaesthetic, Ramon Llull, Alcohol Dehydrogenase, Cellular Respiration, Cellulose Acetate, Carbureted Compression Ignition Model Engines (2010)
Tatsuya Yoshino et al.
Organic letters, 14(16), 4290-4292 (2012-08-09)
A highly efficient total synthesis of the 11-membered cyclic aspercyclides A (1) and B (2) has been achieved by chemo- and regioselective intramolecular oxidative C-O bond formation from differently substituted diphenols.
Ether-directed ortho-C-H olefination with a palladium(II)/monoprotected amino acid catalyst.
Gang Li et al.
Angewandte Chemie (International ed. in English), 52(4), 1245-1247 (2012-12-15)
Faysal Benaskar et al.
ChemSusChem, 6(2), 353-366 (2012-11-30)
A μ(2)-process in the Ullmann-type C-O coupling of potassium phenolate and 4-chloropyridine was successfully performed in a combined microwave (MW) and microflow process. Selective MW absorption in a micro-fixed-bed reactor (μ-FBR) by using a supported Cu nanocatalyst resulted in an

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