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Merck
CN

67268

Myricitrin

analytical standard

Synonym(s):

3,3′,4′,5,5′,7-Hexahydroxyflavone 3-O-rhamnoside, Myricetin 3-O-α-L-rhamnopyranoside, Myricetin 3-O-rhamnoside, Myricitroside

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About This Item

Empirical Formula (Hill Notation):
C21H20O12
CAS Number:
Molecular Weight:
464.38
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
85151701
EC Number:
241-856-7
MDL number:
Technical Service
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grade

analytical standard

Quality Level

assay

≥95.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

food and beverages

format

neat

storage temp.

2-8°C

SMILES string

C[C@@H]1O[C@@H](OC2=C(Oc3cc(O)cc(O)c3C2=O)c4cc(O)c(O)c(O)c4)[C@H](O)[C@H](O)[C@H]1O

InChI

1S/C21H20O12/c1-6-14(26)17(29)18(30)21(31-6)33-20-16(28)13-9(23)4-8(22)5-12(13)32-19(20)7-2-10(24)15(27)11(25)3-7/h2-6,14,17-18,21-27,29-30H,1H3/t6-,14-,17+,18+,21-/m0/s1

InChI key

DCYOADKBABEMIQ-OWMUPTOHSA-N

General description

Myricitrin is a plant compound, isolated from Folium Rhododendri Micranthi, which acts as a nitric oxide and protein kinase inhibitor and is found to exhibit antipsychotic-like effect in animal models.

Application

Myricitrin may be used as an analytical reference standard for determination of the analyte in Folium Rhododendri Micranthi extract using high-performance liquid chromatography. It may also be used as an external standard in the validation of both commercial herbal medicines and crude material of Myrcia uniflora extracts using high-performance liquid chromatography technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.


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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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Wei Chen et al.
Food chemistry, 141(2), 927-933 (2013-06-26)
Peroxynitrite, a potent oxidising and nitrating species, has been implicated in the pathogenesis of neurodegenerative diseases. This study was undertaken to investigate the protective effect of myricitrin on peroxynitrite-mediated toxicity and the underlying mechanism. Our results showed that the presence
Flavia Carla Meotti et al.
The Journal of pharmacology and experimental therapeutics, 316(2), 789-796 (2005-11-02)
The present study investigated the antinociceptive effects of the flavonoid myricitrin in chemical behavioral models of pain in mice and rats. Myricitrin given by i.p. or p.o. routes produced dose-related antinociception when assessed on acetic acid-induced visceral pain in mice.
Dyskinesias: New Insights for the Healthcare Professional: 2012 Edition: ScholarlyBrief, 47(8), 714-717 (2012)



Global Trade Item Number

SKUGTIN
67268-10MG04061832735252