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Merck

439029

Sigma-Aldrich

甲醇-d4

≥99.8 atom % D, contains 0.1 % (v/v) TMS

别名:

全氘代甲醇, 四氘代甲醇

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About This Item

线性分子式:
CD3OD
CAS号:
分子量:
36.07
Beilstein:
1733278
EC號碼:
MDL號碼:
分類程式碼代碼:
12142201
PubChem物質ID:
NACRES:
NA.21

同位素純度

≥99.8 atom % D

品質等級

化驗

≥99% (CP)

形狀

liquid

包含

0.1 % (v/v) TMS

expl. lim.

5.5-36.5 % (lit.)

技術

NMR: suitable

雜質

≤0.025% water
water

折射率

n20/D 1.326 (lit.)

bp

65.4 °C (lit.)

mp

-99 °C (lit.)

密度

0.888 g/mL at 25 °C (lit.)

SMILES 字串

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

InChI

1S/CH4O/c1-2/h2H,1H3/i1D3,2D

InChI 密鑰

OKKJLVBELUTLKV-MZCSYVLQSA-N

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一般說明

Methanol-d4 (CD3OD) is a deuterated NMR solvent containing 0.1% (v/v) TMS (tetramethylsilane). It is useful in NMR-based research and analyses. Absolute infrared absorption intensities of CD3OD have been reported between 8000 and 350cm-1.

應用

Methanol-d4 may be used as a solvent to analyze the rate of exchange of methoxyl group in camphor and norcamphor dimethyl ketals.

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附屬品

产品编号
说明
价格

訊號詞

Danger

危險分類

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

51.8 °F - closed cup

閃點(°C)

11 °C - closed cup


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Infrared intensities of liquids. XVII. Infrared refractive indices from 8000 to 350 cm-1, absolute integrated absorption intensities, transition moments, and dipole moment derivatives of methan-d3-ol and methanol-d4 at 25?C.
Bertie JE and Zhang SL.
J. Chem. Phys. , 101(10), 8364-8379 (1994)
The Rates of Methoxyl Exchange of Camphor and Norcamphor Dimethyl Ketals in Methanol-d4.
Traylor TG and Perrin CL.
Journal of the American Chemical Society, 88(21), 4934-4942 (1966)
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A straightforward synthesis of novel, 2-heterocyclyl polyhydroxylated pyrrolidines is described. Stereocontrolled additions of nucleophiles to cyclic nitrones generated the corresponding 2,3-trans adducts, allowing the synthesis of the corresponding pyrrolidines via key intermediates bearing an alkyne and a nitrile oxide. Three
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For the successful implementation of Distributed Drug Discovery (D(3)) (outlined in the accompanying Perspective), students, in the course of their educational laboratories, must be able to reproducibly make new, high quality, molecules with potential for biological activity. This article reports

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