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Oleuropein - ≥98%, high purity , CAS No.32619-42-4

Moligand™
≥98%

CAS#: 32619-42-4
Formula: C₂₅H₃₂O₁₃
Molecular Weight: 540.51
EC Number: 251-129-6
MDL number: MFCD16879008
PubChem CID: 5281544

Item Number

O140217

Grouped product items
SKU	Size	Availability	Price
O140217-10mg	10mg	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$38.90
O140217-25mg	25mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$77.90
O140217-50mg	50mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$124.90
O140217-100mg	100mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$199.90

Basic Description

Synonyms	Oleuropein\|32619-42-4\|Oleoeuropein\|oleoeuropeine\|2-(3,4-Dihydroxyphenyl)ethyl (2S-(2alpha,3E,4beta))-3-ethylidene-2-(beta-D-glucopyranosyloxy)-3,4-dihydro-5-(methoxycarbonyl)-2H-pyran-4-acetate\|2O4553545L\|methyl (4S,5E,6S)-4-[2-[2-(3,4-dihydroxyphenyl)eth
Specifications & Purity	Moligand™, ≥98%
Biochemical and Physiological Mechanisms	Oleuropein has been shown to augment the secretion of noradrenaline and adrenaline in rat.
Storage Temp	Store at 2-8°C,Argon charged
Shipped In	Wet ice
Grade	Moligand™
Product Description	The primary phenolic compound found in olives and olive oil. Oleuropein hydrolyzes to form hydroxytyrosol and tyrosol, with hydroxytyrosol considered the main component associated with olive′s health benefits. Olive oil phenols demonstrate antioxidant, anti-thrombotic, anti-inflammatory and anti-atherogenic characteristics. An antioxidant and immunomodulator in vitro that is a tyrosol ester derivative of elenolic acid and phenolic glycoside found naturally olive oil.

Associated Targets

HDAC6 Tclin Histone deacetylase 6 0 Activities

Discover Target: HDAC6

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

TAS2R8 Tchem Taste receptor type 2 member 8 0 Activities

Discover Target: TAS2R8

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

ALOX5 Tclin Arachidonate 5-lipoxygenase 0 Activities

Discover Target: ALOX5

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Names and Identifiers

IUPAC Name	methyl (4S,5E,6S)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate
INCHI	InChI=1S/C25H32O13/c1-3-13-14(9-19(29)35-7-6-12-4-5-16(27)17(28)8-12)15(23(33)34-2)11-36-24(13)38-25-22(32)21(31)20(30)18(10-26)37-25/h3-5,8,11,14,18,20-22,24-28,30-32H,6-7,9-10H2,1-2H3/b13-3+/t14-,18+,20+,21-,22+,24-,25-/m0/s1
InChi Key	RFWGABANNQMHMZ-ZCHJGGQASA-N
Canonical SMILES	CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O
Isomeric SMILES	C/C=C/1\[C@@H](C(=CO[C@H]1O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O
WGK Germany	3
PubChem CID	5281544
Molecular Weight	540.51

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5 results found

Lot Number	Certificate Type	Date	Item
L2315523	Certificate of Analysis	Dec 25, 2023	O140217
L2315524	Certificate of Analysis	Dec 25, 2023	O140217
K2316080	Certificate of Analysis	Nov 24, 2023	O140217
G23151131	Certificate of Analysis	Jul 21, 2023	O140217
J2213947	Certificate of Analysis	Oct 18, 2022	O140217

Chemical and Physical Properties

Solubility	Soluble in water, acetone, ethanol, pyridine, glacial acetic acid , 5% aq NaOH, dioxane, butano, ethyl acetate, butyl acetate, DMF (50 mg/ml), and methanol. Insoluble in ether, chloroform, petr ether, benzene, and carbon tetrachloride.
Sensitivity	Hygroscopic
Specific Rotation[α]	-165° (C=0.5,EtOH)
Melt Point(°C)	89 °C

WGK Germany

Merck Index

6830

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