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Merck

177970

Sigma-Aldrich

吡啶-d5

"100%", ≥99.96 atom % D

别名:

氘代吡啶

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About This Item

经验公式(希尔记法):
C5D5N
CAS号:
分子量:
84.13
Beilstein:
114377
EC號碼:
MDL號碼:
分類程式碼代碼:
12142201
eCl@ss:
39151701
PubChem物質ID:
NACRES:
NA.11

品質等級

同位素純度

≥99.96 atom % D

化驗

≥99% (CP)

形狀

liquid

expl. lim.

0.34-6.3 % (lit.)

技術

NMR: suitable

雜質

≤0.05% water
water

折射率

n20/D 1.506 (lit.)

pH值

8.5 (0.2 g/L)

bp

114.4 °C (lit.)

mp

-41 °C (lit.)

密度

1.05 g/mL at 25 °C (lit.)

質量偏移

M+5

SMILES 字串

[2H]c1nc([2H])c([2H])c([2H])c1[2H]

InChI

1S/C5H5N/c1-2-4-6-5-3-1/h1-5H/i1D,2D,3D,4D,5D

InChI 密鑰

JUJWROOIHBZHMG-RALIUCGRSA-N

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一般說明

Pyridine-d5 is a deuterated form of pyridine having an isotopic purity of 99.96atom%D. It is 100% isotopically enriched NMR (Nuclear Magnetic Resonance) solvent. It is widely employed for high resolution NMR studies due to its high chemical and isotopic purity. The reaction between pyridine vapor and heavy water in the presence of a palladium catalyst has been reported to afford pyridine-d5. Infrared (IR), Raman (in the range 300-4000cm-1) and high-resolution (0.06cm-1) FT-IR (Fourier transform infrared) spectral studies of pyridine-d5 have been reported.

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象形圖

FlameExclamation mark

訊號詞

Danger

危險分類

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

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

62.6 °F

閃點(°C)

17 °C

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Slide 1 of 1

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The FT-IR spectra of pyridine and pyridine-d51.
Wong KN and Colson SD.
Journal of Molecular Spectroscopy, 104(1), 129-151 (1984)
Vibrational spectra of C2v deuterium substituted pyridines. 4-pyridine-2, 3, 5, 6-d4 and pyridine-d5.
Stidham HD and Dilella DP.
Journal of Raman Spectroscopy, 9(4), 247-256 (1980)
Shao-Dan Chen et al.
Fitoterapia, 102, 67-73 (2015-02-24)
Five new diarylheptanoids (1-5), along with nine known ones (6-14), were isolated from the rhizomes of Curcuma kwangsiensis. Their structures were established on the basis of spectroscopic analyses. Compounds 1-3 were cyclic diarylheptanoids rarely discovered from C. kwangsiensis. Of all
Yu Shan et al.
Molecules (Basel, Switzerland), 20(11), 20334-20340 (2015-11-17)
A new nortriterpene saponin, 3-O-β-d-glucuronopyranosyl-30-norolean-12,20(29)-dien-23- oxo-28-oic acid, namely bigelovii D (11), was isolated from the hydroalcoholic extract of herbs of Salicornia bigelovii along with 10 known saponins (1-10). Their chemical structures were identified on the basis of spectroscopic analyses including
Indra Prakash et al.
Natural product communications, 9(8), 1135-1138 (2014-09-23)
We report the isolation and complete structure of an isomer of rebaudioside D, known as rebaudioside D2. This novel steviol glycoside was isolated from a bioconversion reaction of rebaudioside A to rebaudioside D. Rebaudioside D2 possesses a relatively rare 1

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