93540
Tropic acid
purum, ≥99.0% (T)
Synonym(s):
2-Phenylhydracrylic acid, 3-Hydroxy-2-phenylpropionic acid
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About This Item
Linear Formula:
C6H5CH(CH2OH)CO2H
CAS Number:
Molecular Weight:
166.17
EC Number:
209-020-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
2209199
MDL number:
grade
purum
assay
≥99.0% (T)
mp
116-118 °C
solubility
methanol: 0.1 g/mL, clear
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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Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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
[Polarographic determination of indomethacin ester using tropic acid].
M Poctová et al.
Ceskoslovenska farmacie, 28(8), 344-346 (1979-10-01)
The biosynthesis of shikimate metabolites.
A R Knaggs
Natural product reports, 18(3), 334-355 (2001-07-31)
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
Separation of tropic and atropic acids by partition and chromatography.
S GOTTLIEB
Journal of the American Chemical Society, 70(1), 423-423 (1948-01-01)
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