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Merck
CN

569550

乙腈-D3

≥99.8 atom % D, anhydrous

别名:

氘代乙腈, 氘代乙腈-D3

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线性分子式:
CD3CN
化学文摘社编号:
分子量:
44.07
UNSPSC Code:
12142201
NACRES:
NA.21
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1740230
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产品名称

乙腈-D3, ≥99.8 atom % D, anhydrous

InChI

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

SMILES string

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

InChI key

WEVYAHXRMPXWCK-FIBGUPNXSA-N

grade

anhydrous

isotopic purity

≥99.8 atom % D

assay

≥99% (CP)

form

liquid

expl. lim.

3.0-16 % (lit.)

technique(s)

NMR: suitable

impurities

>10 ppm 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

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Application

Acetonitrile-d3 may be used as:
  • IR and NMR solvent.
  • Probe for zeolite acidity.
  • Cartridge eluent in HPLC– SPE (solid-phase extraction)–NMR technique.

Other Notes

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pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

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

存储类别

3 - Flammable liquids

wgk

WGK 2

flash_point_f

35.6 °F - closed cup

flash_point_c

2.00 °C - closed cup

法规信息

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分析证书(COA)

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Dynamics of a wetting liquid in nanopores: An optical Kerr effect study of the dynamics of acetonitrile confined in sol-gel glasses.
Loughnane BJ, et al.
J. Chem. Phys. , 111(11), 5116-5123 (1999)
Organic deuterium compounds: XVI. Synthesis of α-deuterated alkyl nitriles.
Leitch LC.
Canadian Journal of Chemistry, 35(4), 345-347 (1957)
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)
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)
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

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