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309966

Sigma-Aldrich

Dietiletere

≥99.9%, suitable for HPLC, inhibitor-free

Sinonimo/i:

Etere, Etil etere

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About This Item

Formula condensata:
(CH3CH2)2O
Numero CAS:
Peso molecolare:
74.12
Beilstein:
1696894
Numero CE:
Numero MDL:
Codice UNSPSC:
12190000
ID PubChem:
NACRES:
NA.07

product name

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

Densità del vapore

2.6 (vs air)

Livello qualitativo

Tensione di vapore

28.69 psi ( 55 °C)
8.59 psi ( 20 °C)

Saggio

≥99.9%

Forma fisica

liquid

Temp. autoaccensione

320 °F

Purificato mediante

glass distillation

Limite di esplosione

36.5 %

tecniche

HPLC: suitable

Impurezze

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

Residuo dopo evaporazione

<0.0003%

Indice di rifrazione

n20/D 1.3530 (lit.)

P. eboll.

34.6 °C (lit.)

Punto di fusione

−116 °C (lit.)

Densità

0.706 g/mL at 25 °C (lit.)

λ

H2O reference

Assorbanza UV

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

applicazioni

food and beverages

Stringa SMILE

CCOCC

InChI

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

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Categorie correlate

Applicazioni


  • 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).


Prodotti consigliati

Scopri i reagenti LiChropur, ideali per analisi HPLC o LC-MS

Pittogrammi

FlameExclamation mark

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

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

Organi bersaglio

Central nervous system

Rischi supp

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

-40.0 °F - closed cup

Punto d’infiammabilità (°C)

-40 °C - closed cup


Certificati d'analisi (COA)

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Sigma-Aldrich

179272

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Dietiletere for analysis EMPARTA&#174; ACS

Supelco

1.07026

Dietiletere

Dietiletere puriss., contains ~5&#160;mg/L 2,6-di-tert.-butyl-4-methylphenol as stabilizer, meets analytical specification of Ph. Eur., BP, &#8805;99.5% (GC)

Sigma-Aldrich

24004

Dietiletere

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)
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)
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

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