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经验公式(希尔记法):
C9H6O3
化学文摘社编号:
分子量:
162.14
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
EC Number:
202-240-3
Beilstein/REAXYS Number:
127683
MDL number:
InChI
1S/C9H6O3/c10-7-3-1-6-2-4-9(11)12-8(6)5-7/h1-5,10H
SMILES string
Oc1ccc2C=CC(=O)Oc2c1
InChI key
ORHBXUUXSCNDEV-UHFFFAOYSA-N
grade
analytical standard
assay
≥98.0% (HPLC)
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
mp
230 °C (dec.) (lit.)
application(s)
food and beverages
format
neat
storage temp.
2-8°C
Quality Level
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General description
Umbelliferone is a naturally occurring coumarin, present in a variety of medicinal plants from the Apiaceae (Umbelliferae) family and also in plants from other families such as mouse-ear hawkweed.
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Umbelliferone may be used as an analytical reference standard for the determination of the analyte in Aegle marmelos fruit using reversed-phase high performance liquid chromatography. It is also used as a template for the synthesis of molecularly imprinted polymers used in the analysis of plant samples.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Other Notes
This compound is commonly found in plants of the genus: angelica glycyrrhiza pimpinella
存储类别
11 - Combustible Solids
wgk
WGK 3
Pharmacognosy And Pharmacobiotechnology, 51(9), 2251-2255 (2003)
Application of umbelliferone molecularly imprinted polymer in analysis of plant samples
Chemical Papers, 67(5), 477-483 (2013)
Rapid simultaneous determination of marmelosin, umbelliferone and scopoletin from Aegle marmelos fruit by RP-HPLC
Shinde.B.P, et al.
Journal of Food Science and Technology, 51(9), 2251-2255 (2014)
Hiromu Kashida et al.
Bioorganic & medicinal chemistry, 20(14), 4310-4315 (2012-06-19)
In this study, we synthesized a simple but efficient quencher-free molecular beacon tethering 7-hydroxycoumarin on D-threoninol based on its pK(a) change. The pK(a) of 7-hydroxycoumarin in a single strand was determined as 8.8, whereas that intercalated in the duplex was
Kalyan K Sadhu et al.
Organic & biomolecular chemistry, 11(4), 563-568 (2012-10-13)
The design and synthesis of molecular probes competent for pH signaling within or beyond a certain range is a complicated matter. Herein a new mechanism for ''OFF-ON-OFF'' absorbance and fluorescence intensities vs. pH behaviour is described. The probe design is
实验方案
HPTLC fingerprinting enables rapid identification of passion flower with related reference materials.
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