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About This Item
Empirical Formula (Hill Notation):
C8H15NO
CAS Number:
Molecular Weight:
141.21
Beilstein:
80188
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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
Joshua G Schier et al.
Academic emergency medicine : official journal of the Society for Academic Emergency Medicine, 11(4), 329-334 (2004-04-06)
A massive nerve agent attack may rapidly deplete in-date supplies of atropine. The authors considered using atropine beyond its labeled shelf life. The objective was to determine the stability of premixed injectable atropine sulfate samples with different expiration dates. This
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
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
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