(2H5)Ethan(2H)ol

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Names

[ CAS No. ]:
1516-08-1

[ Name ]:
(2H5)Ethan(2H)ol

[Synonym ]:
EINECS 216-162-2
(H)Ethan(H)ol
Ethan-d-ol-d
MFCD00051020
1,1,1,2,2-pentadeuterio-2-deuteriooxyethane
Ethyl alcohol-d6,Ethyl-d5 alcohol-d,Hexadeuteroethanol

Chemical & Physical Properties

[ Density]:
0.8±0.1 g/cm3

[ Boiling Point ]:
72.6±3.0 °C at 760 mmHg

[ Melting Point ]:
-130ºC(lit.)

[ Molecular Formula ]:
C2D6O

[ Molecular Weight ]:
52.105

[ Flash Point ]:
8.9±0.0 °C

[ Exact Mass ]:
52.079525

[ PSA ]:
20.23000

[ LogP ]:
-0.19

[ Vapour Pressure ]:
82.8±0.2 mmHg at 25°C

[ Index of Refraction ]:
1.354

[ Storage condition ]:
Flammables area

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS02

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H225

[ Precautionary Statements ]:
P210

[ Hazard Codes ]:
F

[ Risk Phrases ]:
R11

[ Safety Phrases ]:
S7-S16

[ RIDADR ]:
UN 1170 3

[ WGK Germany ]:
1

[ Packaging Group ]:
II

[ Hazard Class ]:
3.0

Precursor & DownStream

Precursor

  • Ethanol

DownStream

  • Bromoethane
  • 3,3-Dimethyl-1-butene
  • Iodoethane-d5
  • Diethyl ether-D10
  • 1,1,2,2-tetradeuterioethene
  • (2H5)Ethyl (2H3)acetate
  • Ethylphenidate

Articles

An Efficient Synthesis of Aurone Derivatives by the Tributylphosphine-catalyzed Regioselective Cyclization of o-Alkynoylphenols. Saito K, et al.

Chem. Lett. 44(2) , 141-143, (2015)

Ethanol-induced changes in neuronal membrane order. An NMR study. Hitzemann RJ, et al.

Biochim. Biophys. Acta 859(2) , 189-197, (1986)


More Articles

Related Compounds

  • (1,1-2H2)Ethan(2H)ol
  • 2-(2H)Sulfanyl(2H4)ethan(2H)ol
  • 2,2',2''-Nitrilotri(2H4)ethan(2H)ol
  • 2,2,2-Trifluoro(2H2)ethan(2H)ol
  • 1-phenylethanol-O-d
  • Diethylamine-d11
  • 3-(3-Acetamidoprop-1-yn-1-yl)pyridine-4-carboxylic acid
  • 2-acetamido-1H-indole-3-carboxylic acid
  • 2-[N-(3-cyanophenyl)acetamido]acetic acid
  • rac-(2R,4R)-4-methyl-1-[(prop-2-en-1-yloxy)carbonyl]piperidine-2-carboxylic acid
  • tert-butyl N-(6,6,6-trifluoro-5-hydroxy-2-methylhexan-3-yl)carbamate
  • tert-butyl N-[2-(aminomethyl)-4-methylpent-1-en-3-yl]carbamate
  • tert-butyl N-[1-(3-methoxyazetidin-3-yl)-3-methylbutan-2-yl]carbamate
  • rac-tert-butyl N-{1-[(1R,2R)-2-(aminomethyl)cyclopropyl]-2-methylpropyl}carbamate
  • tert-butyl N-(6-bromo-2,5,5-trimethylhexan-3-yl)carbamate
  • 1-(1-Acetyl-4-hydroxypiperidin-4-yl)cyclopropane-1-carboxylic acid
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