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Key Documents

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:
Molecular Weight:
141.21
Beilstein:
80188
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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

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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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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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
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
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
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
[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)

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