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Merck

366544

Acetonitrile-d3

99.8 atom % D, contains 0.03 % (v/v) TMS

Synonym(s):

Methyl-d3 cyanide, Trideuteroacetonitrile

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About This Item

Linear Formula:
CD3CN
CAS Number:
2206-26-0
Molecular Weight:
44.07
UNSPSC Code:
12142201
NACRES:
NA.21
PubChem Substance ID:
24862666
EC Number:
218-616-5
Beilstein/REAXYS Number:
1740230
MDL number:
MFCD00001881
Isotopic purity:
99.8 atom % D
Assay:
99% (CP)
Mass shift:
M+3
Form:
liquid

Key Documents

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Product Name

Acetonitrile-d3, 99.8 atom % D, contains 0.03 % (v/v) TMS

InChI key

WEVYAHXRMPXWCK-FIBGUPNXSA-N

InChI

1S/C2H3N/c1-2-3/h1H3/i1D3

SMILES string

[2H]C([2H])([2H])C#N

isotopic purity

99.8 atom % D

assay

99% (CP)

form

liquid

contains

0.03 % (v/v) TMS

expl. lim.

3.0-16 % (lit.)

technique(s)

NMR: suitable

impurities

≤0.02% water
water

refractive index

n20/D 1.341 (lit.)

bp

80.7 °C (lit.)

mp

-46 °C (lit.)

density

0.844 g/mL at 25 °C (lit.)

mass shift

M+3

Quality Level

200

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Application

Acetonitrile-d3 was used as a solvent to record Raman spectrum.
It may be used as:
  • IR and NMR solvent.
  • Probe for zeolite acidity.
  • Cartridge eluent in HPLC- SPE (solid-phase extraction)-NMR technique.

General description

Acetonitrile-d3 (CD3CN), an organo deutero compound, is an α-deuterated alkyl nitrile. Its synthesis from acetonitrile by base-catalyzed exchange with deuterium oxide has been reported. Its molecular rotational friction coefficient has been determined by measuring 2H and 14N nuclear magnetic resonance spin–lattice relaxation times. Its orientational dynamics in nanoporous glasses has been studied using optical Kerr effect spectroscopy.

Other Notes

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pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

35.6 °F - closed cup

flash_point_c

2.00 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
MBBF1176
MBBF0422
MBBD9855
MBBD8381
MBBD8380

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The lowest triplet state of 1, 3, 5-hexatrienes: Quantum chemical force field calculations and experimental resonance Raman spectra.
Negri F, et al.
J. Chem. Phys. , 90(11), 5944-5963 (1989)
Maja Lambert et al.
Magnetic resonance in chemistry : MRC, 43(9), 771-775 (2005-07-29)
The HPLC-SPE-NMR technique was used for the analysis of a root-bark extract of Croton membranaceus. The components of the extract were separated on an analytical-size reversed-phase HPLC column, the chromatographic peaks were trapped on SPE (solid-phase extraction) cartridges after post-column
Acetonitrile-d3 as a probe of Lewis and Broensted acidity of zeolites.
Pelmenschikov AG, et al.
The Journal of Physical Chemistry, 97(42), 11071-11074 (1993)
Proton polarizability caused by collective proton motion in intramolecular chains formed by two and three hydrogen bonds. Implications for charge conduction in bacteriorhodopsin.
Brzezinski B, et al.
The Journal of Physical Chemistry, 91(11), 3077-3080 (1987)
Organic deuterium compounds: XVI. Synthesis of α-deuterated alkyl nitriles.
Leitch LC.
Canadian Journal of Chemistry, 35(4), 345-347 (1957)
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