Melting point	122-125 ºC
Water Solubility	sparingly soluble in code water

Symbol(GHS)	Xi
Hazard Codes	R36/37/38
SDS/MSDS	S26;S37/39

Source	SDS/MSDS Samples
没有数据	没有数据

Synthetic Route

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Name	CAS

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Articles

Peer-Reviewed Papers

Aptamer-targeted delivery of Bcl-xL shRNA using alkyl modified PAMAM dendrimers into lung cancer cells.Sara Ayatollahi et al.The international journal of biochemistry & cell biology, 92, 210-217 (2017-10-17) Heme-coordinating analogs of lauric acid as inhibitors of fatty acid omega-hydroxylation.P Lu et al.Archives of biochemistry and biophysics, 337(1), 1-7 (1997-01-01) Synthesis of efficient gene delivery systems by grafting pegylated alkylcarboxylate chains to PAMAM dendrimers: Evaluation of transfection efficiency and cytotoxicity in cancerous and mesenchymal stem cells.Sara Ayatollahi et al.Journal of biomaterials applications, 30(5), 632-648 (2015-08-13) Smart liposomal drug delivery for treatment of oxidative stress model in human embryonic stem cell-derived retinal pigment epithelial cells.Farnaz Behroozi et al.International journal of pharmaceutics, 548(1), 62-72 (2018-05-29) Comparison study of the effect of alkyl-modified and unmodified PAMAM and PPI dendrimers on solubility and antitumor activity of crocetin.Fatemeh Soltani et al.Artificial cells, nanomedicine, and biotechnology, 45(7), 1356-1362 (2016-11-01) Alkylcarboxylate grafting to polyethylenimine: a simple approach to producing a DNA nanocarrier with low toxicity.Reza K Oskuee et al.The journal of gene medicine, 11(10), 921-932 (2009-07-28) Effects of sulfur-containing analogues of stearic acid on growth and fatty acid biosynthesis in the protozoan Crithidia fasciculata.M D Rahman et al.Journal of medicinal chemistry, 31(8), 1656-1659 (1988-08-01) The synthesis and functional evaluation of a mitochondria-targeted hydrogen sulfide donor,(10-oxo-10-(4-(3-thioxo-3 h-1, 2-dithiol-5-yl) phenoxy) decyl) triphenylphosphonium bromide (Ap39).Le Trionnaire S, et al. MedChemComm, 5(6), 728-736 (2014) Anodic Syntheses Involving ω-Monohalocarboxylic Acids1. Pattison FLM, et al. Journal of the American Chemical Society, 78(10), 2255-2259 (1956)

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