7212-69-3
Chemical Structure
Dioleyldimethylammonium chloride
Synonym(s): DODAC
- CAS No.: 7212-69-3
- Formula:C38H76ClN
- Molecular Weight:582.47
IUPAC Name: (Z)-N,N-dimethyl-N-((Z)-octadec-9-en-1-yl)octadec-9-en-1-aminium chloride
InChIKey: UAKOZKUVZRMOFN-JDVCJPALSA-M
SMILES: CCCCCCCC/C=C\CCCCCCCC[N+](C)(C)CCCCCCCC/C=C\CCCCCCCC.[Cl-]
Biological Activity: Dioleyldimethylammonium chloride (DODAC) is a positively charged lipid promoter with membrane-disrupting activity, which is often formulated into cationic liposomes with dioleoylphosphatidylethanolamine. Dioleyldimethylammonium chloride is used in gene transfection research; through electrostatic interactions, it effectively promotes the binding of programmable fusion vesicles to cells and induces membrane disruption. Dioleyldimethylammonium chloride is also applied in studies on L1210 leukemia and LS180 human colon cancer[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Dioleyldimethylammonium chloride | 95.88% | Dioleyldimethylammonium chloride (DODAC) is a positively charged lipid promoter with membrane-disrupting activity, which is often formulated into cationic liposomes with dioleoylphosphatidylethanolamine. Dioleyldimethylammonium chloride is used in gene transfection research; through electrostatic interactions, it effectively promotes the binding of programmable fusion vesicles to cells and induces membrane disruption. Dioleyldimethylammonium chloride is also applied in studies on L1210 leukemia and LS180 human colon cancer. | ||||||||||||||||||||
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Similarity Score 0.82
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Similarity Score 0.82
HY-W010731Dicetyldimonium bromide -
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Similarity Score 0.78
HY-184793Oleyl palmitamide -
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HY-117016Nonacosadiene -
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HY-1125277(Z),11(Z)-Heptacosadiene -
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References
- [1]. Lee S Y, et al. Stimulation of phospholipase D in HepG2 cells after transfection using cationic liposomes[J]. Bulletin of the Korean Chemical Society, 2013, 34(3): 931-935.
- [2]. Adlakha-Hutcheon G, et al. Controlled destabilization of a liposomal drug delivery system enhances mitoxantrone antitumor activity. Nat Biotechnol. 1999;17(8):775-779. [Content Brief]
