850330 | 11:0 PC



Size SKU Packaging Price
25mg 850330P-25mg 850330P-25mg 1 x 25mg $104.00
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11:0 PC

11:0 PC


The list of Phosphatidylcholine products offered by Avanti is designed to provide compounds having a variety of physical properties. Products available include short chain (C3-C8 are water soluble and hygroscopic), saturated, multi-unsaturated and mixed acid PC's. All of the products are purified by HPLC, and special precautions are taken to protect the products from oxidization and hydrolysis. Several of these products are manufactured under the current guidelines of Good Manufacturing Practice and are available for pharmaceutical use. If you have a requirement for a choline derivative not found on our list, please call us: custom synthesis is one of our specialties.

Light Sensitive
Molecular Formula
Percent Composition
C 60.68%, H 10.19%, N 2.36%, O 21.56%, P 5.22%
1 Years
Storage Temperature
CAS Number
CAS Registry Number is a Registered Trademark of the American Chemical Society
Formula Weight
Exact Mass

Wen SY, Chen YY, Lu JX, Liang QQ, Shi H, Wu Q, Yao ZH, Zhu Y, Jiang MM. Modulation of hepatic lipidome by rhodioloside in high-fat diet fed apolipoprotein E knockout mice. Phytomedicine. 2020 Apr;69:152690. doi: 10.1016/j.phymed.2018.09.225. Epub 2018 Sep 27. PMID: 30389273.

PubMed ID: 30389273

Miaomiao Jiang, Jingyu Ni, Yuanlin Cao, Xiaoxue Xing, Qian Wu, and Guanwei Fan, “Astragaloside IV Attenuates Myocardial Ischemia-Reperfusion Injury from Oxidative Stress by Regulating Succinate, Lysophospholipid Metabolism, and ROS Scavenging System,” Oxidative Medicine and Cellular Longevity, vol. 2019, Article ID 9137654, 17 pages, 2019. doi: 10.1155/2019/9137654.

Abe Y, Honsho M, Itoh R, Kawaguchi R, Fujitani M, Fujiwara K, Hirokane M, Matsuzaki T, Nakayama K, Ohgi R, Marutani T, Nakayama KI, Yamashita T, Fujiki Y. Peroxisome biogenesis deficiency attenuates the BDNF-TrkB pathway-mediated development of the cerebellum. Life Sci Alliance. 2018 Dec 3;1(6):e201800062. doi: 10.26508/lsa.201800062. eCollection 2018 Dec.

PubMed ID: 30519675

Tanaka AJ, Okumoto K, Tamura S, Abe Y, Hirsch Y, Deng L, Ekstein J, Chung WK, Fujiki Y. A newly identified mutation in the PEX26 gene is associated with a milder form of Zellweger spectrum disorder. Cold Spring Harb Mol Case Stud. 2019 Feb 1;5(1). pii: a003483. doi: 10.1101/mcs.a003483. Print 2019 Feb.

PubMed ID: 30446579