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Lignoceric acid - >99.0%(GC), high purity , CAS No.557-59-5
Long chain saturated fatty acid
Description générale
Synonymes
tetraicosanoic acid | EEF1376B-508E-4043-94E9-AC29747EA6AB | FA 24:0 | AKOS015892947 | LIGNOCERIC ACID [MI] | N-TETRACOSANOIC ACID | tetracosanic acid | Tetracosansaeure | UNII-RK3VCW5Y1L | RK3VCW5Y1L | CHEBI:28866 | 1219794-59-8 | AS-48043 | MFCD00002810
Spécifications et pureté
≥99%(GC)
Mécanismes biochimiques et physiologiques
Long chain saturated fatty acid. Component of cerebrosides and sphingomyelin. Acyl-CoA ligase substrate. Energy source in vivo . Orally active.
Température de stockage
Store at 2-8°C
Expédié en
Wet ice
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Classe
Fatty Acyls
Subclass
Fatty acids and conjugates
Intermediate Tree Nodes
Not available
Direct Parent
Very long-chain fatty acids
Alternative Parents
Straight chain fatty acids Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic acyclic compounds
Substituents
Very long-chain fatty acid - Straight chain fatty acid - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
Description
This compound belongs to the class of organic compounds known as very long-chain fatty acids. These are fatty acids with an aliphatic tail that contains at least 22 carbon atoms.
External Descriptors
Straight chain fatty acids
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.
Cibles associées (humaines)
Mécanismes d'action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
Références
Noms et identifiants
Pubchem Sid
504752080
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504752080
IUPAC Name
tetracosanoic acid
INCHI
InChI=1S/C24H48O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24(25)26/h2-23H2,1H3,(H,25,26)
InChIKey
QZZGJDVWLFXDLK-UHFFFAOYSA-N
Smiles
CCCCCCCCCCCCCCCCCCCCCCCC(=O)O
Isomères SMILES
CCCCCCCCCCCCCCCCCCCCCCCC(=O)O
WGK Allemagne
3
Poids moléculaire
368.64
Reaxy-Rn
1728237
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1728237&ln=
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
Propriétés chimiques et physiques
Solubilité
Solubility in water: Practically insoluble; Soluble in Chloroform; Very slightly soluble in Ethanol
Point d'ébullition (°C)
272°C
Point de fusion (°C)
82°C-86°C
Poids moléculaire
368.600 g/mol
XLogP3
10.700
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
22
Exact Mass
368.365 Da
Monoisotopic Mass
368.365 Da
Topological Polar Surface Area
37.300 Ų
Heavy Atom Count
26
Formal Charge
0
Complexity
275.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Yang Zhang, Xiaowen Liu, Guojing Yu, Hongzhe Gui, Jingteng Chi, Shuhan Liu, Liang Fang, Mingzhe Liu.
(2023)
Innovative insight into the mechanism of enantioselective skin permeation for chiral drugs. Expert Opinion on Drug Delivery,
2.
Jie Li, Ting He, Hongyu Chen, Yangming Cheng, Enrico Drioli, Zhaohui Wang, Zhaoliang Cui.
(2023)
Preparation of Hyflon AD/Polypropylene Blend Membrane for Artificial Lung. Membranes,
13
(7):
(665).
3.
Shiqiang Cheng, Jiajie Hu, Chen Guo, Zhicheng Ye, Yazhuo Shang, Cheng Lian, Honglai Liu.
(2023)
The effects of size and surface functionalization of polystyrene nanoplastics on stratum corneum model membranes: An experimental and computational study. JOURNAL OF COLLOID AND INTERFACE SCIENCE,
638
(778).
4.
Shuzhen Dou, Zhongshun Wang, Qiye Chen, Nan Lu.
(2022)
One-step fabrication of high-density Si nanotips as SALDI-MS substrate for highly sensitive detection. SENSORS AND ACTUATORS B-CHEMICAL,
359
(131578).
5.
Tao Wang, Xingyue Liu, Xuetong Qu, Yuexin Li, Xiao Liang, Jianmin Wu.
(2021)
Lipid response of hepatocellular carcinoma cells to anticancer drug detected on nanostructure-assisted LDI-MS platform. TALANTA,
235
(122817).
6.
Xinrong Jiang, Xiaoming Chen, Tao Wang, Yuexin Li, Aiwu Pan, Jianmin Wu.
(2021)
Perfluorinated polymer modified vertical silicon nanowires as ultra low noise laser desorption ionization substrate for salivary metabolites profiling. TALANTA,
225
(122022).
7.
Xiaoming Chen, Tao Wang, Leimiao Lin, Fangjie Wo, Yaqin Liu, Xiao Liang, Hui Ye, Jianmin Wu.
(2018)
Tip-Enhanced Photoinduced Electron Transfer and Ionization on Vertical Silicon Nanowires. ACS Applied Materials & Interfaces,
10
(17):
(14389–14398).
8.
Guo XiaoYu, Zhou Jianglu, Yu Hong, Cao Han, Li Xia, Hu Qing, Yu YunQiu.
(2024)
Serum lipidomic study of long-chain fatty acids in psoriasis patients prior to and after anti-IL-17A monoclonal antibody treatment by quantitative GC‒MS analysis with in situ extraction. Lipids in Health and Disease,
23
(1):
(1-15).
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8 Citations
H2420340