An acyl choline
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Isomer(s)
37482Carbaethopendecine (bromide)
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Palmitoylcholine (chloride)

Item No. 9003456

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
N,N,N-trimethyl-2-[(1-oxohexadecyl)oxy]-ethanaminium, monochloride
CAS Number
2932-74-3
Molecular Formula
C21H44NO2 • Cl
Formula Weight
378.0
Purity
≥95%
Formulation (Request formulation change)
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 20 mg/mlDMSO: 14 mg/mlEthanol: 20 mg/ml
SMILES
CCCCCCCCCCCCCCCC(OCC[N+](C)(C)C)=O.[Cl-]
InChi Code
InChI=1S/C21H44NO2.ClH/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-21(23)24-20-19-22(2,3)4;/h5-20H2,1-4H3;1H/q+1;/p-1
InChi Key
SABHLWJWDCWCRQ-UHFFFAOYSA-M
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    5 mg

    $128

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    10 mg

    $215

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    25 mg

    $503

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    Product Description

    Palmitoylcholine is an acyl choline.1 It inhibits protein kinase C activity when used at a concentration of 100 μM.2 Palmitoylcholine induces hemolysis in rat erythrocytes.3 Plasma levels of palmitoylcholine are decreased in female patients with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS).1

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Germain, A., Barupal, D.K., Levine, S.M., et al. Comprehensive circulatory metabolomics in ME/CFS reveals disrupted metabolism of acyl lipids and steroids. Metabolites 10(1), 34 (2020).

    2. Nakadate, T., and Blumberg, P.M. Modulation by palmitoylcarnitine of protein kinase C activation. Cancer Res. 47(24 Pt 1), 6537-6542 (1987).

    3. Cho, K.S., and Proulx, P. Interactions of acyl carnitines and other lysins with erythrocytes and reconstituted erythrocyte lipoproteins. Biochim. Biophys. Acta 318(1), 50-60 (1973).