860516 | C16 Ceramide (d18:1/16:0)

N-palmitoyl-D-erythro-sphingosine


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5mg 860516P-5mg 860516P-5mg 1 x 5mg $67.00
10mg 860516P-10mg 860516P-10mg 1 x 10mg $126.00
25mg 860516P-25mg 860516P-25mg 1 x 25mg $263.00
50mg 860516P-50mg 860516P-50mg 1 x 50mg $483.00
100mg 860516P-100mg 860516P-100mg 1 x 100mg $756.00
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C16 Ceramide (d18:1/16:0)

C16 Ceramide (d18:1/16:0)

N-palmitoyl-D-erythro-sphingosine

Hygroscopic
No
Light Sensitive
No
Molecular Formula
C34H67NO3
Percent Composition
C 75.92%, H 12.55%, N 2.60%, O 8.92%
Purity
>99%
Stability
1 Years
Storage Temperature
-20°C
CAS Number
24696-26-2
CAS Registry Number is a Registered Trademark of the American Chemical Society
Molecular Weight
537.901
Exact Mass
537.512
Synonyms
<p>N-(hexadecanoyl)-sphing-4-enine</p>

Fanani ML, Busto JV, Sot J, Abad JL, Fabrías G, Saiz L, Vilar JMG, Goñi FM, Maggio B, Alonso A. Clearly Detectable, Kinetically Restricted Solid-Solid Phase Transition in cis-Ceramide Monolayers. Langmuir. 2018 Sep 24. doi: 10.1021/acs.langmuir.8b02198. [Epub ahead of print]

PubMed ID: 30183303

Peñalva DA, Oresti GM, Dupuy F, Antollini SS, Maggio B, Aveldaño MI, Fanani ML. Atypical surface behavior of ceramides with nonhydroxy and 2-hydroxy very long-chain (C28-C32) PUFAs. Biochim Biophys Acta. 2014 Mar;1838(3):731-8. doi: 10.1016/j.bbamem.2013.11.018. Epub 2013 Dec 5.

PubMed ID: 24315999

Ceramide-Induced Lamellar Gel Phases in Fluid Cell Lipid Extracts Aritz B. García-Arribas, Hasna Ahyayauch, Jesús Sot, Pablo L. López-González, Alicia Alonso, and Félix M. Goñi Langmuir 2016, 32, 9053−9063 Al Sazzad, M.A. and J.P. Slotte. (2016).

PubMed ID: 27486830

Effect of Phosphatidylcholine Unsaturation on the Lateral Segregation of Palmitoyl Ceramide and Palmitoyl Dihydroceramide in Bilayer Membranes. Langmuir

PubMed ID: 27218704

Lonnfors, M., O. Langvik, A. Bjorkbom, and J.P. Slotte. (2013). Cholesteryl Phosphocholine - A Study on Its Interactions with Ceramides and Other Membrane Lipids. Langmuir

PubMed ID: 23356741

Matsufuji T, Kinoshita M, Möuts A, Slotte JP, Matsumori N Preparation and Membrane Properties of Oxidized Ceramide Derivatives. Langmuir. 2017 Dec 27. doi: 10.1021/acs.langmuir.7b02654.

PubMed ID: 29231736

Perera MN, Ganesan V, Siskind LJ, Szulc ZM, Bielawski J, Bielawska A, Bittman R, Colombini M. Ceramide channels: influence of molecular structure on channel formation in membranes. Biochim Biophys Acta. 2012 May;1818(5):1291-301. doi: 10.1016/j.bbamem.2012.02.010. Epub 2012 Feb 15.

PubMed ID: 22365970

Perera MN, Ganesan V, Siskind LJ, Szulc ZM, Bielawska A, Bittman R, Colombini M. Ceramide channel: Structural basis for selective membrane targeting. Chem Phys Lipids. 2016 Jan;194:110-116. doi: 10.1016/j.chemphyslip.2015.09.007. Epub 2015 Sep 25.

PubMed ID: 26408265

Bockelmann S, Mina JGM, Korneev S, Hassan DG, Mueller D, Hilderink A, Vlieg HC, Raijmakers R, Heck AJR, Haberkant P, Holthuis JCM. A search for ceramide binding proteins using bifunctional lipid analogs yields CERT-related protein StarD7. J Lipid Res. 2018 Jan 17. pii: jlr.M082354. doi: 10.1194/jlr.M082354. [Epub ahead of print]

PubMed ID: 29343537