An internal standard for the quantification of (±)-linalool
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Unlabeled Version(s)
21575(±)-Linalool
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(±)-Linalool-d3

Item No. 9004273

Technical Information
Formal Name
3,7-dimethyl-1,6-octadien-1,1,2-d3-3-ol
CAS Number
1216673-02-7
Synonyms
  • dl-Linalool-d3
Molecular Formula
C10H15D3O
Formula Weight
Purity
≥99% deuterated forms (d1-d3)
A neat oil
Chloroform: Slightly solubleEthyl Acetate: Slightly solubleMethanol: Slightly soluble
SMILES
C/C(C)=C/CCC(O)(C)/C([2H])=C([2H])/[2H]
InChi Code
InChI=1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3/i1D2,5D
InChi Key
CDOSHBSSFJOMGT-WSWICNJZSA-N
Origin
Synthetic
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    (±)-Linalool-d3 is intended for use as an internal standard for the quantification of (±)-linalool (Item No. 21575) by GC- or LC-MS. (±)-Linalool is a monoterpene alcohol that has been found in C. sativa, C. indica, and hemp with diverse biological activities.1,2,3,4,5,6 It induces cell cycle arrest at the G0/G1 and G2M phase in U937 and HeLa cells, respectively.2 (±)-Linalool is cytotoxic to U937 and HeLa cells (IC50s = 2.59 and 11.02 μM, respectively). It induces recruitment of a PGC-1α coactivator peptide to the PPARα ligand binding domain (EC50 = 5.45 μM in a TR-FRET assay).3 In vivo, (±)-linalool reduces plasma triglyceride concentration in mice fed a Western diet and transgenic mice expressing human ApoE2, but not PPARα-/- mice. It has molluscicidal and larvicidal effects in vitro (LC50s = 0.25 and 0.07 mg/L for O. hupensis and S. japonicium, respectively), and it reduces the amount of schistosomulum recovered from mouse skin after S. japonicium challenge infection.4 (±)-Linalool (10-40 mg/kg) reduces the number of macrophages and neutrophils, as well as the production of TNF-α, IL-6, IL-1β, IL-8, and MCP-1, in bronchoalveolar lavage fluid (BALF) in a mouse model of cigarette smoke-induced acute lung inflammation.5 It also decreases immobility time in the forced swim test in mice, indicating antidepressant-like activity.6

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Hazekamp, A., Tejkalová, K., and Papadimitriou, S. Cannabis: From cultivar to chemovar II—A metabolomics approach to Cannabis classification. Cannabis Cannabinoid Res. 1(1), 202-215 (2016).

    2. Ständer, S., Ständer, H., Seeliger, S., et alTopical pimecrolimus and tacrolimus transiently induce neuropeptide release and mast cell degranulation in murine skin. Br. J. Dermatol. 156(5), 1020-1026 (2007).

    3. Jun, H.J., Lee, J.H., Kim, J., et alLinalool is a PPARα ligand that reduces plasma TG levels and rewires the hepatic transcriptome and plasma metabolome. J. Lipid. Res. 55(6), 1098-1110 (2014).

    4. Yang, F., Long, E., Wen, J., et alLinalool, derived from Cinnamomum camphora (L.) Presl leaf extracts, possesses molluscicidal activity against Oncomelania hupensis and inhibits infection of Schistosoma japonicum. Parasit. Vectors 7, 407 (2014).

    5. Jianqun, M., Hai, X., Wu, J., et alLinalool inhibits cigarette smoke-induced lung inflammation by inhibiting NF-κB activation. Int. Immunopharmacol. 29(2), 708-713 (2015).

    6. Guzmán-Gutiérrez, S.L., Bonilla-Jaime, H., Gómez-Cansino, R., et alLinalool and β-pinene exert their antidepressant-like activity through the monoaminergic pathway. Life Sci. 128, 24-29 (2015).