93550
Tropine
≥97.0% (NT)
Synonym(s):
3-Tropanol
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About This Item
Empirical Formula (Hill Notation):
C8H15NO
CAS Number:
Molecular Weight:
141.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-384-2
Beilstein/REAXYS Number:
80188
MDL number:
Assay:
≥97.0% (NT)
Form:
powder
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
SMILES string
CN1[C@H]2CC[C@@H]1C[C@H](O)C2
assay
≥97.0% (NT)
form
powder
impurities
0-3% water
solubility
H2O: 0.1 g/mL, clear
functional group
hydroxyl
storage temp.
2-8°C
Quality Level
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Related Categories
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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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.
A Yamashita et al.
Biochemistry, 38(24), 7630-7637 (1999-07-01)
Tropinone reductase-II (TR-II) catalyzes the NADPH-dependent reduction of the carbonyl group of tropinone to a beta-hydroxyl group. The crystal structure of TR-II complexed with NADP+ and pseudotropine (psi-tropine) has been determined at 1.9 A resolution. A seven-residue peptide near the
Heike Kaiser et al.
Planta, 225(1), 127-137 (2006-07-18)
Tropinone reductases (TRs) are essential enzymes in the tropane alkaloid biosynthesis, providing either tropine for hyoscyamine and scopolamine formation or providing pseudotropine for calystegines. Two cDNAs coding for TRs were isolated from potato (Solanum tuberosum L.) tuber sprouts and expressed
Gábor Maksay et al.
Bioorganic & medicinal chemistry, 17(19), 6872-6878 (2009-09-04)
Heteroaromatic carboxylic esters of (nor)tropine were synthesized. Tropine esters displaced [(3)H]strychnine binding to glycine receptors of rat spinal cord with low Hill slopes. Two-site displacement resulted in nanomolar IC(50,1) and micromolar IC(50,2) values, and IC(50,2)/IC(50,1) ratios up to 615 depending
Rawia Zayed et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 59(11-12), 863-867 (2005-01-26)
Hairy root cultures of Brugmansia suaveolens were set up by infection of root tips with Agrobacterium rhizogenes. The successful transformation was confirmed by analysing rolC and virC genes using polymerase chain reaction (PCR). Hairy root cultures were employed to study
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