Skip to Content
Merck

Skip To

08198

Eleutheroside E

analytical standard

Synonym(s):

[(1R,3aR,4S,6aS)-Tetrahydro-1H,3H-furo[3,4-c]furan-1,4-diyl]bis(2,6-dimethoxy-4,1-phenylene) bis-β-D-glucopyranoside

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View
Pack SizeSKUAvailabilityPrice

About This Item

Empirical Formula (Hill Notation):
C34H46O18
CAS Number:
Molecular Weight:
742.72
NACRES:
NA.24
UNSPSC Code:
85151701
Pricing and availability is not currently available.
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


grade

analytical standard

Quality Level

assay

≥98.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

application(s)

food and beverages

format

neat

storage temp.

2-8°C

SMILES string

COc1cc(cc(OC)c1O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]3OC[C@@H]4[C@@H]3CO[C@H]4c5cc(OC)c(O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)c(OC)c5

InChI

1S/C34H46O18/c1-43-17-5-13(6-18(44-2)31(17)51-33-27(41)25(39)23(37)21(9-35)49-33)29-15-11-48-30(16(15)12-47-29)14-7-19(45-3)32(20(8-14)46-4)52-34-28(42)26(40)24(38)22(10-36)50-34/h5-8,15-16,21-30,33-42H,9-12H2,1-4H3/t15?,16?,21-,22+,23-,24+,25+,26-,27-,28+,29?,30?,33+,34-

InChI key

FFDULTAFAQRACT-RGFZIUCCSA-N

General description

Eleutheroside E is one of the major bioactive saponins of Eleutherococcus senticosus.

Application

Eleutheroside E (ELU E) may be used as a reference standard for the analysis of ELU E in:
  • Rat plasma and tissue by solid-phase extraction (SPE) followed by high-performance liquid chromatography (HPLC) and photodiode array detection (PDA).
  • Acanthopanax senticosus by ionic liquids-ultrasound assisted extraction (ILUAE) followed by HPLC with ultraviolet (UV) detection.[1]
  • Eleutherococcus senticosus Maxim. by rapid resolution liquid chromatography (RRLC) equipped with multi-wavelength UV detector.[2]
  • Acanthopanax giraldii Harms by HPLC with diode array detector (DAD).

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Compare Similar Items

View Full Comparison

Show Differences

1 of 1

This Item
SMB007011234680PHL89190
grade

analytical standard

grade

-

grade

pharmaceutical primary standard

grade

primary reference standard

format

neat

format

-

format

neat

format

neat

application(s)

food and beverages

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

application(s)

pharmaceutical (small molecule)

application(s)

food and beverages

assay

≥98.0% (HPLC)

assay

≥97%

assay

-

assay

≥95.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

shelf life

-

shelf life

-

shelf life

-

Quality Level

100

Quality Level

200

Quality Level

-

Quality Level

-


Still not finding the right product?

Explore all of our products under Eleutheroside E


Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



Semipreparative separation and determination of eleutheroside E in Acanthopanax giraldii Harms by high-performance liquid chromatography
Wang Z, et al.
Journal of Chromatographic Science, 43(5), 249-252 (2005)
D H Kim et al.
Archives of pharmacal research, 22(1), 30-34 (1999-03-11)
When liriodendrin or syringin was incubated for 24 h with human intestinal bacteria, two metabolites, (+)-syringaresinol-beta-D-glucopyranoside and (+)-syringaresinol, from liriodendrin and one metabolite, synapyl alcohol, from syringin were produced. The metabolic time course of liriodendrin was as follows: at early
L B Kardono et al.
Journal of natural products, 53(6), 1447-1455 (1990-11-01)
By bioactivity-directed fractionation, six cytotoxic constituents have been characterized from the bark of Plumeria rubra collected in Indonesia. Three iridoids, fulvoplumierin [1], allamcin [2], and allamandin [3], as well as 2,5-dimethoxy-p-benzoquinone [4], were found to be active constituents of the



Global Trade Item Number

SKUGTIN
P50900-1G04061834376057
P50900-5G04061834376118
P50900-250G04061833403440
P50900-25G04061834376064
08198-10MG04061838652225

Questions

Reviews

No rating value

Active Filters