A 22-carbon monounsaturated fatty acid
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13(Z)-Docosenoic Acid

Item No. 90175

Technical Information
Formal Name
13Z-docosenoic acid
CAS Number
112-86-7
Synonyms
  • C22:1(13Z)
  • C22:1 n-9
  • cis-13-Docosenoic Acid
  • Erucic Acid
  • FA 22:1
Molecular Formula
C22H42O2
Formula Weight
Purity
≥98%
A 250 mg/ml solution in ethanol
0.1 M Tris-HCl, pH 8: 1 mg/mlDMF: 100 mg/mlDMSO: 100 mg/mlEthanol: MisciblePBS (7.2): 100 µg/ml
SMILES
CCCCCCCC/C=C\CCCCCCCCCCCC(=O)O
InChi Code
InChI=1S/C22H42O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24/h9-10H,2-8,11-21H2,1H3,(H,23,24)/b10-9-
InChi Key
DPUOLQHDNGRHBS-KTKRTIGZSA-N
Side Chain Carbon Sum
22:1
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    13(Z)-Docosenoic acid is a 22-carbon monounsaturated fatty acid. It is found predominantly in canola oil.1 13(Z)-Docosenoic acid is metabolized to oleic acid in vivo. Diets rich in 13(Z)-docosenoic acid were shown to cause heart lipidosis in experimental animals.2,3 The C-1 amide of docosenoic acid has been identified as one of the anandamide-related neurotransmitters associated with sleep.4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Borg, K. Physiopathological effects of rapeseed oil: A review. Acta Med. Scand. Suppl. 585, 5-13 (1975).

    2. Hulan, H.W., Kramer, J.K.G., Mahadevan, S., et alRelationship between erucic acid and myocardial changes in male rats. Lipids 11(1), 9-15 (1975).

    3. Astorg, P.O. Heart lipidosis induced by short-term feeding of cis- or trans-docosenoic acids in weanling or 7-week-old rats. Ann. Nutr. Metab. 25(4), 201-207 (1981).

    4. Cravatt, B.F., Prospero-Garcia, O., Siuzdak, G., et alChemical characterization of a family of brain lipids that induce sleep. Science 268(5216), 1506-1509 (1995).