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Supelco

Scopoletin

analytical standard

Sinônimo(s):

6-Methoxyumbelliferone, 6-Methylesculetin, 7-Hydroxy-6-methoxy-2H-1-benzopyran-2-one, 7-Hydroxy-6-methoxycoumarin, Buxuletin, Chrysatropic acid, Escopoletin, Esculetin-6-methyl ether, Gelseminic acid, Murrayetin

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About This Item

Fórmula empírica (Notação de Hill):
C10H8O4
Número CAS:
92-61-5
Peso molecular:
192.17
Beilstein:
156296
Número CE:
202-171-9
Número MDL:
MFCD00006872
Código UNSPSC:
85151701
ID de substância PubChem:
329755673
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

Ensaio

≥97.0% (HPLC)

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

pf

203-205 °C (lit.)

aplicação(ões)

food and beverages

formato

neat

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

COc1cc2C=CC(=O)Oc2cc1O

InChI

1S/C10H8O4/c1-13-9-4-6-2-3-10(12)14-8(6)5-7(9)11/h2-5,11H,1H3

chave InChI

RODXRVNMMDRFIK-UHFFFAOYSA-N

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Descrição geral

Scopoletin is a coumarin compound and pharmacologically active chemical that is found in various plant species.

Aplicação

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Scopoletin may be used as a reference standard for the determination of scopoletin in:
  • Roots, stems, branches, and seeds as well as leaves of Chimonanthus nitens Oliv. by ultra-high performance liquid chromatography/tandem quadrupole-time-of-flight mass spectrometry (UHPLC-QTOF-MS/MS) equipped with modified mass deflect filter or diagnostic product ions/neutral loss filter.
  • Canscora decussate (South Indian Shankhpushpi) extracts by high performance thin layer chromatography (HPTLC).
  • Morinda tinctoria Roxb. leaf by HPTLC in conjunction with HPLC and gas chromatography with MS.

Ações bioquímicas/fisiológicas

Scopoletin significantly increases activity of lipoprotein lipase in adipocytes by promoting transcription of the LPL gene. It also partially reverses inhibition of LPL by TNF-α.

Embalagem

Bottomless glass bottle. Contents are inside inserted fused cone.

Outras notas

This compound is commonly found in plants of the genus: achillea angelica glycyrrhiza lycium pimpinella

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Choose from one of the most recent versions:

Certificados de análise (COA)

Lot/Batch Number
BCCG8916
BCCF6742
BCCC8260
BCBZ9692
BCBX3994

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Sigma-Aldrich

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HPTLC Finger print analysis and Phytochemical Investigation of Morinda tinctoria Roxb. Leaf extracts by HPLC and GS MS.
Arunachalam KD, et al.
International Journal of Pharmacy and Pharmaceutical Sciences, 7(2), 360-366 (2015)
Structural characterization and discrimination of Chimonanthus nitens Oliv. leaf from different geographical origins based on multiple chromatographic analysis combined with chemometric methods.
Huang WP, et al.
Journal of Pharmaceutical and Biomedical Analysis, 154(2-3), 236-244 (2018)
Comprehensive profiling and characterization of coumarins from roots, stems, leaves, branches, and seeds of Chimonanthus nitens Oliv. using ultra-performance liquid chromatography/quadrupole-time-of-flight mass spectrometry combined with modified mass defect filter.
Tan T, et al.
Journal of Pharmaceutical and Biomedical Analysis, 141(2-3), 140-148 (2017)
Use of scopoletin to inhibit the production of inflammatory cytokines through inhibition of the I?B/NF-?B signal cascade in the human mast cell line HMC-1.
Moon PD, et al.
European Journal of Pharmacology, 555(2-3), 218-225 (2007)
Rapid validated high performance thin layer chromatography method for simultaneous estimation of mangiferin and scopoletin in Canscora decussata (South Indian Shankhpushpi) extract.
Sethiya NK, et al.
Revista Brasileira de Farmacognosia, 25(3), 193-198 (2015)
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