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About This Item
Linear Formula:
C6H5CH(CH2OH)CO2H
CAS Number:
Molecular Weight:
166.17
Beilstein:
2209199
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
grade
reagent grade
product line
Vetec™
Assay
98%
mp
116-118 °C (lit.)
SMILES string
OCC(C(O)=O)c1ccccc1
InChI
1S/C9H10O3/c10-6-8(9(11)12)7-4-2-1-3-5-7/h1-5,8,10H,6H2,(H,11,12)
InChI key
JACRWUWPXAESPB-UHFFFAOYSA-N
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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The biosynthesis of shikimate metabolites.
A R Knaggs
Natural product reports, 18(3), 334-355 (2001-07-31)
M Eeva et al.
Journal of pharmaceutical and biomedical analysis, 16(5), 717-722 (1998-04-16)
A capillary zone electrophoretic method (CZE) was developed using an uncoated fused silica capillary for the separation and determination of the main tropane alkaloids. The applicability of the developed method for analysis of plant samples was examined by analyzing samples
Patrick K Harrison et al.
Naunyn-Schmiedeberg's archives of pharmacology, 373(3), 230-236 (2006-06-01)
The enzyme atropinesterase (EC 3.1.1.10) causes the rapid hydrolysis of tropane alkaloids such as atropine and scopolamine. This enzyme is known to occur in a certain proportion of rabbits and some plants, although its presence in other animal species remains
Stephanie Heine et al.
Electrophoresis, 24(15), 2687-2692 (2003-08-06)
A method for the separation of atropine enantiomers, D- and L-hyoscyamine by capillary electrophoresis (CE) has been developed and validated. The advantages of the CE method compared with polarimetry include smaller amounts of analytes and a lower limit of detection
Simultaneous determination of atropine sulphate and tropic acid by reversed phase high-pressure liquid chromatography.
A Richard et al.
Die Pharmazie, 39(12), 866-867 (1984-12-01)
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