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611697

Sigma-Aldrich

Ethanol-d6

95% in D2O, 99 atom % D

Synonym(s):

Ethyl alcohol-d6, Ethyl-d5 alcohol-d, Hexadeuteroethanol

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About This Item

Linear Formula:
CD3CD2OD
CAS Number:
1516-08-1
Molecular Weight:
52.11
Beilstein:
1699096
EC Number:
216-162-2
MDL number:
MFCD00051020
UNSPSC Code:
12142201
PubChem Substance ID:
329759375

isotopic purity

99 atom % D

Assay

99% (CP)

expl. lim.

3.5-15 % (lit.)

concentration

95% in D2O

technique(s)

NMR: suitable

refractive index

n20/D 1.358 (lit.)

bp

78 °C (lit.)

mp

-130 °C (lit.)

density

0.892 g/mL at 25 °C

mass shift

M+6

SMILES string

[2H]OC([2H])([2H])C([2H])([2H])[2H]

InChI

1S/C2H6O/c1-2-3/h3H,2H2,1H3/i1D3,2D2,3D

InChI key

LFQSCWFLJHTTHZ-LIDOUZCJSA-N

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Application

Ethanol-d6 may be used as a solvent for the tributylphosphine (PBu3) induced 5-exo cyclization of o-alkynoylphenol to form deuterated aurone.

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Statements

H225,H319

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

55.4 °F - closed cup

Flash Point(C)

13 °C - closed cup

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Ethanol-induced changes in neuronal membrane order. An NMR study.
Hitzemann RJ, et al.
Biochimica et Biophysica Acta, 859(2), 189-197 (1986)
Johannes B Laurens et al.
Journal of forensic and legal medicine, 58, 155-163 (2018-07-08)
Sterile ante-mortem blood specimens were spiked with ethanol at the South African blood alcohol legal concentration limits of 0.20 g/L and 0.50 g/L and were stored in tubes containing sodium fluoride over a period of twenty-nine weeks under refrigeration (4 °C) and at
An Efficient Synthesis of Aurone Derivatives by the Tributylphosphine-catalyzed Regioselective Cyclization of o-Alkynoylphenols.
Saito K, et al.
Chemistry Letters (Jpn), 44(2), 141-143 (2015)

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