Juniperic acid

Juniperic acid
Names
	IUPAC name 16-Hydroxyhexadecanoic acid
	Other names 16-Hydroxypalmitic acid; omega-Hydroxypalmitic acid; ω-Hydroxypalmitic acid;
Identifiers
CAS Number	506-13-8;
3D model ( JSmol)	Interactive image;
ChEBI	CHEBI:55328;
ChEMBL	ChEMBL4281719;
ChemSpider	10034;
ECHA InfoCard	100.007.299
EC Number	208-028-7;
KEGG	C18218;
PubChem CID	10466;
CompTox Dashboard (EPA)	DTXSID6060133 ;
	InChI InChI=1S/C16H32O3/c17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16(18)19/h17H,1-15H2,(H,18,19) Key: UGAGPNKCDRTDHP-UHFFFAOYSA-N;
	SMILES C(CCCCCCCC(=O)O)CCCCCCCO;
Properties
Chemical formula	C16H32O3
Molar mass	272.429 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Juniperic acid or 16-hydroxyhexadecanoic acid is an omega-hydroxy long-chain fatty acid that is palmitic acid which is substituted at position 16 by a hydroxy group. Palmitic acid is converted to juniperic acid by cytochrome P450 various enzymes,^[1] including CYP704B22.^[2]

Juniperic acid is a key monomer of cutin in the plant cuticle.^[3] It has a role as a plant metabolite.

References

S2CID 22920318
.

PMID 20086189
.

^ "Metabocard for 16-Hydroxyhexadecanoic acid (HMDB0006294)". The Metabolomics Innovation Centre.

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[1] S2CID 22920318
.

[2] PMID 20086189
.

[3] "Metabocard for 16-Hydroxyhexadecanoic acid (HMDB0006294)". The Metabolomics Innovation Centre.

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