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93550

Sigma-Aldrich

Tropine

≥97.0% (NT)

Synonym(s):

3-Tropanol

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About This Item

Empirical Formula (Hill Notation):
C8H15NO
CAS Number:
120-29-6
Molecular Weight:
141.21
Beilstein/REAXYS Number:
80188
EC Number:
204-384-2
MDL number:
MFCD00005551
UNSPSC Code:
12352100
PubChem Substance ID:
57653567
NACRES:
NA.22

assay

≥97.0% (NT)

form

powder

impurities

0-3% water

solubility

H2O: 0.1 g/mL, clear

storage temp.

2-8°C

SMILES string

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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Related Categories

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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B A Bartholomew et al.
The Biochemical journal, 307 ( Pt 2), 603-608 (1995-04-15)
Tropine dehydrogenase was induced by growth of Pseudomonas AT3 on atropine, tropine or tropinone. It was NADP(+)-dependent and gave no activity with NAD+. The enzyme was very unstable but a rapid purification procedure using affinity chromatography that gave highly purified
Grit Rothe et al.
Journal of experimental botany, 54(390), 2065-2070 (2003-07-30)
Putrescine N-methyltransferase (PMT) is the first alkaloid-specific enzyme for nicotine and tropane alkaloid formation. The pmt gene from Nicotiana tabacum was fused to the CaMV 35S promoter and integrated into the Atropa belladonna genome. Transgenic plants and derived root cultures
Interference of mandelic acid with the determination of homatropine hydrobromide by second-order derivative spectroscopy.
J S Millership
Journal of pharmaceutical and biomedical analysis, 12(9), 1199-1203 (1994-09-01)
Gábor Maksay et al.
Bioorganic & medicinal chemistry, 16(4), 2086-2092 (2007-12-07)
(Hetero)aromatic mono- and diesters of tropine and nortropine were prepared. Modulation of [3H]strychnine binding to glycine receptors of rat spinal cord was examined with a ternary allosteric model. The esters displaced [3H]strychnine binding with nano- or micromolar potencies and strong
Birgit Dräger
Phytochemistry, 67(4), 327-337 (2006-01-24)
Two stereospecific oxidoreductases constitute a branch point in tropane alkaloid metabolism. Products of tropane metabolism are the alkaloids hyoscyamine, scopolamine, cocaine, and polyhydroxylated nortropane alkaloids, the calystegines. Both tropinone reductases reduce the precursor tropinone to yield either tropine or pseudotropine.
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