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Merck
CN

93550

Sigma-Aldrich

托品碱

≥97.0% (NT)

别名:

品托碱

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About This Item

经验公式(希尔记法):
C8H15NO
CAS号:
分子量:
141.21
Beilstein:
80188
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

≥97.0% (NT)

表单

powder

杂质

0-3% water

溶解性

H2O: 0.1 g/mL, clear

官能团

hydroxyl

储存温度

2-8°C

SMILES字符串

CN1[C@H]2CC[C@@H]1C[C@H](O)C2

InChI

1S/C8H15NO/c1-9-6-2-3-7(9)5-8(10)4-6/h6-8,10H,2-5H2,1H3/t6-,7+,8+

InChI key

CYHOMWAPJJPNMW-JIGDXULJSA-N

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储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Laszlo Gyermek et al.
Journal of critical care, 24(1), 58-65 (2009-03-11)
There is a need for neuromuscular relaxant (NMR) agents that are of the "nondepolarizing type" and produce rapidly developing and short-lasting skeletal muscle relaxation in anesthesiology. Many efforts have been directed to produce such agents. Our research focused on the
Renata A Kwiecień et al.
Archives of biochemistry and biophysics, 510(1), 35-41 (2011-03-23)
(15)N heavy isotope effects are especially useful when detail is sought pertaining to the reaction mechanism for the cleavage of a C-N bond. Their potential in assisting to describe the mechanism of N-demethylation of tertiary amines by the action of
Patrick Giraudeau et al.
Journal of pharmaceutical and biomedical analysis, 43(4), 1243-1248 (2006-11-23)
Quantitative analysis by (1)H NMR is often hampered by heavily overlapping signals that may occur for complex mixtures, especially those containing similar compounds. Bidimensional homonuclear NMR spectroscopy can overcome this difficulty. A thorough review of acquisition and post-processing parameters was
[Studies on the synthesis and neuromuscular-blocking activity of symmetrical bis-and poly-quaternary derivatives of quinuclidine and tropine].
S Q Chen et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 22(5), 347-353 (1987-05-01)
Amit K Kushwaha et al.
Gene, 516(2), 238-247 (2012-12-26)
Tropinone reductases (TRs) are small proteins belonging to the SDR (short chain dehydrogenase/reductase) family of enzymes. TR-I and TR-II catalyze the conversion of tropinone into tropane alcohols (tropine and pseudotropine, respectively). The steps are intermediary enroute to biosynthesis of tropane

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