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P0359

Palmitoylethanolamide

≥98% (HPLC), powder, cannabinoid receptor agonist

Synonym(s):

N-(2-Hydroxyethyl)hexadecanamide, PEA, Palmidrol

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About This Item

Empirical Formula (Hill Notation):
C18H37NO2
CAS Number:
544-31-0
Molecular Weight:
299.49
NACRES:
NA.77
PubChem Substance ID:
24278619
UNSPSC Code:
12352200
EC Number:
208-867-9
MDL number:
MFCD00020562

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Product Name

Palmitoylethanolamide,

InChI key

HXYVTAGFYLMHSO-UHFFFAOYSA-N

InChI

1S/C18H37NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18(21)19-16-17-20/h20H,2-17H2,1H3,(H,19,21)

SMILES string

CCCCCCCCCCCCCCCC(=O)NCCO

form

powder

storage temp.

−20°C

Quality Level

100
200

Gene Information

human ... CNR1(1268), CNR2(1269)
rat ... Faah(29347)

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1 of 4

This Item
SML0906SML0384SML2594
Palmitoylethanolamide

Sigma-Aldrich

P0359

Palmitoylethanolamide

HPOB ≥98% (HPLC)

Sigma-Aldrich

SML0906

HPOB

Eicosapentaenoyl ethanolamide 5 mg/mL in absolute ethanol, ≥98% (HPLC)

Sigma-Aldrich

SML0384

Eicosapentaenoyl ethanolamide

Sapacitabine

Sigma-Aldrich

SML2594

Sapacitabine

form

powder

form

powder

form

solution

form

powder

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

-

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

−20°C

Gene Information

human ... CNR1(1268), CNR2(1269)
rat ... Faah(29347)

Gene Information

-

Gene Information

-

Gene Information

-

Application

Palmitoylethanolamide has been used as a reference standard in mass spectrometry (MS/MS).[1]

Biochem/physiol Actions

Palmitoylethanolamide (PEA) is a natural fatty acid[2] amide of ethanolamine and palmitic acid.[3] It is found in soybeans, egg yolk, and many other food sources.[4] PEA is an endogenous cannabinoid receptor agonist.[5] It is a peroxisome proliferator-activated receptor α (PPAR-α) ligand. PEA possesses anti-inflammatory, anti-allergic[4], neuroprotective, and analgesic activities.[6] It belongs to the class of lipid mediators and the N-acylethanolamine family. PEA blocks the release of pro-inflammatory mediators from activated mast cells and prevents the recruitment of activated mast cells at the site of nerve injury.[2]

Other Notes

Structural analog of anandamide.

signalword

Danger

pictograms

CorrosionEnvironment
GHS05,GHS09

Hazard Classifications

Aquatic Chronic 2 - Eye Dam. 1 - Skin Irrit. 2

Storage Class

13 - Non Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0000502907
0000502906
0000502906
0000502907
0000460767

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Jonathan C van Zijl et al.
Annals of clinical and translational neurology, 5(4), 386-396 (2018-04-25)
Posthypoxic myoclonus (PHM) in the first few days after resuscitation can be divided clinically into generalized and focal (uni- and multifocal) subtypes. The former is associated with a subcortical origin and poor prognosis in patients with postanoxic encephalopathy (PAE), and
Tessa L Crume et al.
American journal of obstetrics and gynecology, 215(5), 609-609 (2016-10-30)
Consistent evidence of an influence of maternal dietary intake during pregnancy on infant body size and composition in human populations is lacking, despite robust evidence in animal models. We sought to evaluate the influence of maternal macronutrient intake and balance
Lili He et al.
Journal of chromatographic science, 54(8), 1428-1434 (2016-05-04)
This article aims to build up a simple, rapid and accurate capillary zone electrophoresis (CZE) method for the separation of biogenic amines (BAs). Here, 10 key BAs (phenethylamine, histamine, tryptamine, tyramine, 5-hydroxytryptamine, octopamine, dopamine, norepinephrine, epinephrine and carnosine) owning significant
Melania Melis et al.
The Laryngoscope, 129(9), E307-E312 (2019-01-25)
Taste sensitivity varies greatly among individuals influencing eating behavior and health, consequently the disorders of this sense can affect the quality of life. The ability to perceive the bitter of thiourea compounds, such as phenylthiocarbamide (PTC), has been largely reported
Didier M Lambert et al.
Current medicinal chemistry, 9(6), 663-674 (2002-04-12)
The discovery of anandamide as an endogenous ligand for the cannabinoid receptors has led to a resurgence of interest in the fatty acid amides. However, N-palmitoylethanolamine (PEA), a shorter and fully saturated analogue of anandamide, has been known since the
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