Hydro Soy PC(HSPC) - ≥98% , CAS No.97281-48-6

CAS: 97281-48-6 Cat. No.: H498541 Numero EC: 306-549-5

GRADE & PURITY ≥98%

Synonyms

Hydrogenated soya phosphatidylcholine | Phosphatidylcholines, soya, hydrogenated | HSPC | Hydrogenated soy phosphatidylcholines | Phosphatidylcholine, PC (soybean, hydrogenated)

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Panoramica

L-α-phosphatidylcholine, hydrogenated (Soy) may be used in the lipososme generation for reconstitution of complement active human plasma, bupivacaine and dexamethasone loading.

Specifications

Sinonimi

Hydrogenated soya phosphatidylcholine | Phosphatidylcholines, soya, hydrogenated | HSPC | Hydrogenated soy phosphatidylcholines | Phosphatidylcholine, PC (soybean, hydrogenated)

Specifiche e purezza

≥98%

Meccanismi biochimici e fisiologici

L-α-phosphatidylcholine, hydrogenated (Soy) is naturally occurring and is majorly used in the synthesizing liposomes. It is also used in small unilamellar vesicles (SUVs) synthesis

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥98%

Nomi e identificatori

• Pubchem Sid: 508813970
• Sorrisi canonici: CCCCCCCCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCCCCCC
• IUPAC Name: 2,3-di(octadecanoyloxy)propyl 2-(trimethylazaniumyl)ethyl phosphate
• InChIKey: NRJAVPSFFCBXDT-UHFFFAOYSA-N
• INCHI: 1S/C44H88NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-30-32-34-36-43(46)50-40-42(41-52-54(48,49)51-39-38-45(3,4)5)53-44(47)37-35-33-31-29-27-25-23-21-19-17-15-13-11-9-7-2/h42H,6-41H2,1-5H3
• Isomeri SMILES: CCCCCCCCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCCCCCC
• Reaxy-Rn: 1899528
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1899528&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Classe Glycerophospholipids
      • Subclass Glycerophosphocholines

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: Glycerophospholipids
• Subclass: Glycerophosphocholines
• Intermediate Tree Nodes: Not available
• Direct Parent: Phosphatidylcholines
• Alternative Parents: Phosphocholines Fatty acid esters Dialkyl phosphates Dicarboxylic acids and derivatives Tetraalkylammonium salts Carboxylic acid esters Organopnictogen compounds Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Amines
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Diacylglycero-3-phosphocholine - Phosphocholine - Fatty acid ester - Dialkyl phosphate - Dicarboxylic acid or derivatives - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Fatty acyl - Quaternary ammonium salt - Tetraalkylammonium salt - Carboxylic acid ester - Carboxylic acid derivative - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Amine - Organic salt - Hydrocarbon derivative - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as phosphatidylcholines. These are glycerophosphocholines in which the two free -OH are attached to one fatty acid each through an ester linkage.
• External Descriptors: a phosphatidylcholine

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Obiettivi associati (non umani)

Rotavirus (147 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Peso molecolare: 790.100 g/mol
• XLogP3: 15.600
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 44
• Exact Mass: 789.625 Da
• Monoisotopic Mass: 789.625 Da
• Topological Polar Surface Area: 111.000 Ų
• Heavy Atom Count: 54
• Formal Charge: 0
• Complexity: 888.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Riferimenti

1. Weiwei Tang, Jiapeng Kang, Lu Yang, Jialin Lin, Jing Song, Dan Zhou, Feng Ye.  (2023)  Thermosensitive nanocomposite components for combined photothermal-photodynamic therapy in liver cancer treatment.  COLLOIDS AND SURFACES B-BIOINTERFACES,      [PMID:37105064] [10.1016/j.colsurfb.2023.113317]

2. Haiying Hua, Nan Zhang, Dan Liu, Lili Song, Tuanbing Liu, Shasha Li, Yongxing Zhao.  (2023)  Multifunctional gold nanorods and docetaxel-encapsulated liposomes for combined thermo- and chemotherapy.  International Journal of Nanomedicine,      [PMID:29123399] [10.2147/IJN.S143977]

3. Yuan Tian, Zhiliang Gao, Ning Wang, Ming Hu, Yi Ju, Qiang Li, Frank Caruso, Jingcheng Hao, Jiwei Cui.  (2022)  Engineering Poly(ethylene glycol) Nanoparticles for Accelerated Blood Clearance Inhibition and Targeted Drug Delivery.  Journal of the American Chemical Society,      [PMID:36166420] [10.1021/jacs.2c06877]

4. Lihui Wen, Mengxin Gan, Siying Xiong, Li Dai, Wen Chen, Wen Shi.  (2025)  Thermosensitive hydrogel composite with si-Cx43 nanoparticles and anti-VEGF agent for synergistic treatment of diabetic retinopathy.  Materials Today Bio,      [PMID:40528841] [10.1016/j.mtbio.2025.101917]

5. Wu Rong, Chen Yanyang, Wu Junyu, Ren Kaixuan, Cui Wenguo, Yin Jingbo.  (2026)  Poly(l-glutamic Acid)-Based Microgels with Long-Term Synergistic Lubrication and MMP-Responsive Anti-Inflammatory Delivery for Osteoarthritis Therapy.  BIOMACROMOLECULES,      [PMID:] [10.1021/acs.biomac.6c00920]