1.07026
Diethyl ether
≥99.5% (GC), EMPARTA® ACS reagent, contains 5-10 ppm 2, 6-Di-tert-butyl-4-methylphenol (BHT) as stabilizer
Synonym(s):
Et2O, Ethoxyethane, Ethyl ether, Ether, Ether, Ethyl ether
About This Item
Recommended Products
product name
Diethyl ether, for analysis EMPARTA® ACS
grade
ACS reagent
Quality Level
vapor density
2.6 (vs air)
vapor pressure
587 hPa ( 20 °C)
product line
EMPARTA®
assay
≥99.5% (GC)
form
liquid
autoignition temp.
320 °F
potency
1215 mg/kg LD50, oral (Rat)
>2000 mg/kg LD50, skin (Rabbit)
contains
5-10 ppm 2,6-Di-tert-butyl-4-methylphenol (BHT) as stabilizer
expl. lim.
36.5 %
impurities
≤0.000015% Peroxide (as H2O2)
≤0.0002 meq/g Titrable acid
≤0.001% Carbonyl compounds (as HCHO)
≤0.1% Water
evapn. residue
≤0.001%
color
clearAPHA: ≤10
refractive index
n20/D 1.3530 (lit.)
bp
34.6 °C (lit.)
mp
−116 °C (lit.)
transition temp
flash point -40 °C
density
0.706 g/mL at 25 °C (lit.)
storage temp.
15-25°C
SMILES string
CCOCC
InChI
1S/C4H10O/c1-3-5-4-2/h3-4H2,1-2H3
InChI key
RTZKZFJDLAIYFH-UHFFFAOYSA-N
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Related Categories
Application
- Inhibition of Food-Borne Pathogen Growth and Biogenic Amine Synthesis by Spice Extracts.: This research explores the efficacy of spice extracts in inhibiting pathogen growth, with diethyl ether used in the extraction process to isolate active compounds (Kuley et al., 2024).
- β-sitosterol isolated from the leaves of Trema orientalis (Cannabaceae) promotes viability and proliferation of BF-2 cells.: Features the use of diethyl ether in the extraction of β-sitosterol, showcasing its application in bioactive compound isolation for medical research (Mekarunothai et al., 2024).
- Solvent Extraction of PDMS Tubing as a New Method for the Capture of Volatile Organic Compounds from Headspace.: Introduces a novel method for capturing volatile organic compounds using diethyl ether, enhancing analytical capabilities in chemical ecology (Thomas et al., 2024).
- Metal Vapour Synthesis of an Organometallic Barium(0) Synthon.: Describes the critical role of diethyl ether in the synthesis of complex organometallic compounds, underlining its utility in advanced materials science (Townrow et al., 2024).
Analysis Note
Identity (IR): conforms
Appearance: clear
Color: ≤ 10 Hazen
Titrable acid: ≤ 0.0002 meq/g
Boiling point: 34 - 35 °C
Peroxide (as H₂O₂): ≤ 0.000015 %
Carbonyl compounds (as HCHO): ≤ 0.001 %
Evaporation residue: ≤ 0.001 %
Water: ≤ 0.1 %
The product is stabilized with 5-10 ppm 2,6-Di-tert-butyl-4-methylphenol (BHT).
Legal Information
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 1 - STOT SE 3
target_organs
Central nervous system
supp_hazards
wgk_germany
WGK 1
flash_point_f
-40.0 °F
flash_point_c
-40 °C
Certificates of Analysis (COA)
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