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346136
Dietiléter
≥99.0%, anhydrous, ACS reagent, contains BHT as inhibitor
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:
12352112
PubChem Substance ID:
NACRES:
NA.07
grade:
ACS reagent
anhydrous
anhydrous
assay:
≥99.0%
bp:
34.6 °C (lit.)
vapor pressure:
28.66 psi ( 55 °C)
8.56 psi ( 20 °C)
8.56 psi ( 20 °C)
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Nombre del producto
Dietiléter, ACS reagent, anhydrous, ≥99.0%, contains BHT as inhibitor
grade
ACS reagent
anhydrous
Quality Level
vapor density
2.6 (vs air)
vapor pressure
28.66 psi ( 55 °C)
8.56 psi ( 20 °C)
assay
≥99.0%
form
liquid
autoignition temp.
320 °F
contains
BHT as inhibitor
expl. lim.
36.5 %
impurities
Alcohol ( as CH3CH2OH ), passes test
≤0.0002 meq/g Titr. acid
≤0.001% Carbonyl ( as HCHO )
≤0.03% water
≤1 ppm Peroxide ( as H2O2)
evapn. residue
≤0.001%
color
APHA: ≤10
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.)
SMILES string
CCOCC
InChI
1S/C4H10O/c1-3-5-4-2/h3-4H2,1-2H3
InChI key
RTZKZFJDLAIYFH-UHFFFAOYSA-N
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General description
Diethyl ether is a versatile organic solvent used in the fields of diesel engines, agriculture, food, chemical, biological, pharmaceutical, and medical industries.
Application
Diethyl ether can be used as a solvent in the:
- Ring-opening polymerization of ε-caprolactone to synthesize polycaprolactone.
- Rh-catalyzed C-H allylation of amides with allyl halides to synthesize allylated amides.
- Photochemical α-bromination of aromatic and aliphatic carbonyl compounds with N-bromosuccinimide to synthesize α-brominated ketones.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Flam. Liq. 1 - STOT SE 3
target_organs
Respiratory system
supp_hazards
Storage Class
3 - Flammable liquids
wgk_germany
WGK 1
flash_point_f
-40.0 °F
flash_point_c
-40 °C
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