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T89605

Sigma-Aldrich

Tropinone

99%

Synonym(s):

8-Methyl-8-azabicyclo[3.2.1]octan-3-one

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About This Item

Empirical Formula (Hill Notation):
C8H13NO
CAS Number:
532-24-1
Molecular Weight:
139.19
Beilstein:
2329
EC Number:
208-530-6
MDL number:
MFCD00005549
UNSPSC Code:
12352100
PubChem Substance ID:
24900577
NACRES:
NA.22

Assay

99%

bp

113 °C/25 mmHg (lit.)

mp

40-44 °C (lit.)

storage temp.

2-8°C

SMILES string

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

InChI

1S/C8H13NO/c1-9-6-2-3-7(9)5-8(10)4-6/h6-7H,2-5H2,1H3/t6-,7+

InChI key

QQXLDOJGLXJCSE-KNVOCYPGSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302 + H332

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

194.0 °F - closed cup

Flash Point(C)

90 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Tropane alkaloid biosynthesis. A century old problem unresolved.
A J Humphrey et al.
Natural product reports, 18(5), 494-502 (2001-11-09)
R Xu et al.
Journal of medicinal chemistry, 41(17), 3220-3231 (1998-08-14)
A number of O-alkynyloximes of tropinone and N-methyl-4-piperidinone have been synthesized and evaluated for muscarinic activity. The affinities of these oximes were tested in homogenates of cerebral cortex, heart, and submandibulary glands from rats using [3H]pirenzepine and [3H]-N-methylscopolamine as radioligands.
Solid-phase synthesis of tertiary N-methyl amines including tropanes.
Michal Sienkiewicz et al.
Journal of combinatorial chemistry, 12(1), 5-8 (2009-11-03)
Jesús Marín-Sáez et al.
Journal of chromatography. A, 1518, 46-58 (2017-09-06)
Tropane alkaloids are a wide group of substances that comprises more than 200 compounds occurring especially in the Solanaceae family. The main aim of this study is the development of a method for the analysis of the principal tropane alkaloids
Some features of modern pharmacology.
V V Zakusov
Pharmacological research communications, 12(3), 233-238 (1980-03-01)
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