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Merck

309966

Sigma-Aldrich

Dietiléter

≥99.9%, suitable for HPLC, inhibitor-free

Sinónimos:

Éter, Éter etílico

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About This Item

Fórmula lineal:
(CH3CH2)2O
Número de CAS:
Peso molecular:
74.12
Beilstein/REAXYS Number:
1696894
EC Number:
MDL number:
UNSPSC Code:
12190000
PubChem Substance ID:
NACRES:
NA.07

product name

Dietiléter, suitable for HPLC, ≥99.9%, inhibitor-free

vapor density

2.6 (vs air)

Quality Level

vapor pressure

28.69 psi ( 55 °C)
8.59 psi ( 20 °C)

assay

≥99.9%

form

liquid

autoignition temp.

320 °F

purified by

glass distillation

expl. lim.

36.5 %

technique(s)

HPLC: suitable

impurities

≤0.03% water
≤1 ppm peroxides (as H2O2)

evapn. residue

<0.0003%

refractive index

n20/D 1.3530 (lit.)

bp

34.6 °C (lit.)

mp

−116 °C (lit.)

density

0.706 g/mL at 25 °C (lit.)

λ

H2O reference

UV absorption

λ: 218 nm Amax: 1.0
λ: 250 nm Amax: 0.20
λ: 275 nm Amax: 0.04
λ: 300-400 nm Amax: 0.01

application(s)

food and beverages

SMILES string

CCOCC

InChI

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

InChI key

RTZKZFJDLAIYFH-UHFFFAOYSA-N

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Application


  • Luminescence of In(III)Cl-etioporphyrin-I.: This study investigates the luminescence properties of In(III)Cl-etioporphyrin-I, employing diethyl ether in the synthesis process to enhance solubility and reaction outcomes (Koptyaev et al., 2023).


  • An efficient synthesis of phosphonated cyclopentenones by NaN(3)-catalyzed three-component reaction between trialkyl phosphites, ethyl arylmethylidenecyanoacetates and dialkyl acetylenedicarboxylates.: Highlights a novel synthesis technique using diethyl ether as a solvent to facilitate the reaction process, crucial for the production of phosphonated cyclopentenones (Ranjbar Derranji and Anary-Abbasinejad, 2024).


  • Antioxidant and Anti-Inflammatory Activities of Phenolic Acid-Rich Extract from Hairy Roots of Dracocephalum moldavica.: Discusses the extraction of phenolic acids using diethyl ether from Dracocephalum moldavica, examining their antioxidant and anti-inflammatory properties (Weremczuk-Jeżyna et al., 2023).

  • [An improved extraction and nonradioactive thin-layer chromatography detection method of mycolic acid].: Describes an improved method for the extraction and analysis of mycolic acid using diethyl ether, enhancing the detection efficiency in biological samples (Xu et al., 2023).


  • A Modified (1)H-NMR Quantification Method of Ephedrine Alkaloids in Ephedrae Herba Samples.: Presents a modified NMR quantification method where diethyl ether plays a critical role in the extraction and preparation of samples for precise measurement of ephedrine alkaloids (Li et al., 2023).


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Pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

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

target_organs

Central nervous system

supp_hazards

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

-40.0 °F - closed cup

flash_point_c

-40 °C - closed cup


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Los clientes también vieron

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Lana S Barkawi et al.
Nature protocols, 5(10), 1609-1618 (2010-10-05)
Auxin measurements in plants are critical to understanding both auxin signaling and metabolic homeostasis. The most abundant natural auxin is indole-3-acetic acid (IAA). This protocol is for the precise, high-throughput determination of free IAA in plant tissue by isotope dilution
Diethyl ether (DEE) as a renewable diesel fuel.
Bailey B, et al.
No. 972978. SAE technical paper (1997)
K H Young et al.
Journal of clinical microbiology, 10(6), 852-853 (1979-12-01)
Ethyl acetate appears to be a satisfactory subsitute solvent for diethyl ether in the Formalin-ether sedimentation technique. In comparative studies, concentration of organisms with ethyl acetate was equal to or greater than that with diethyl ether. No distortion or alteration
Eagleson M.
Concise Encyclopedia Chemistry, 471-471 (1994)
Oxidation of secondary alcohols in diethyl ether with aqueous chromic acid. Convenient procedure for the preparation of ketones in high epimeric purity.
Brown HC, et al.
The Journal of Organic Chemistry, 36(3), 387-390 (1971)

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