Arachidic acid - analytical standard, high purity , CAS No.506-30-9

Item Number
A110477
Grouped product items
SKUSizeAvailabilityPrice Qty
A110477-100mg
100mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$165.90
A110477-500mg
500mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$735.90
A110477-1g
1g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$1,318.90

Basic Description

Synonymsfatty acid 20:0 | NSC93983 | NSC-93983 | DTXCID3040859 | NSC 93983 | Elcosanoic Acid | InChI=1/C20H40O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h2-19H2,1H3,(H,21,22 | C20:0 | PQB8MJD4RB | ARACHIDIC ACID [MI] | BDBM50463966 | CH3-[CH2]18-
Specifications & Purityanalytical standard
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
Gradeanalytical standard
Product Description

A saturated fatty acid found naturally in fish and vegetable oils, and it can also be formed by the hydrogenation of arachidonic acid. Diets rich in saturated fatty acids such as arachidic acid, are known to increase serum low-density lipoproteins resulting in high blood cholesterol levels. Because of its surfactant-like properties, arachidic acid is used in the manufacture of pharmaceuticals, soaps, cosmetics, and food packaging.
A saturated fatty acid.

Associated Targets(Human)

PTPN1 Tchem Tyrosine-protein phosphatase non-receptor type 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TRPV2 Tchem Transient receptor potential cation channel subfamily V member 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ACHE Tclin Acetylcholinesterase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
BCHE Tclin Cholinesterase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PPARA Tclin Peroxisome proliferator-activated receptor alpha (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PPARD Tchem Peroxisome proliferator-activated receptor delta (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PPARG Tclin Peroxisome proliferator-activated receptor gamma (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARA Tclin Peroxisome proliferator-activated receptor alpha (9197 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ptpn1 Protein-tyrosine phosphatase 1B (270 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trpv2 Transient receptor potential cation channel subfamily V member 2 (148 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name icosanoic acid
INCHI InChI=1S/C20H40O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h2-19H2,1H3,(H,21,22)
InChi Key VKOBVWXKNCXXDE-UHFFFAOYSA-N
Canonical SMILES CCCCCCCCCCCCCCCCCCCC(=O)O
Isomeric SMILES CCCCCCCCCCCCCCCCCCCC(=O)O
RTECS JX3780000
PubChem CID 10467
Molecular Weight 312.53
Beilstein 1788211
Reaxy-Rn 1788211

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

Find and download the COA for your product by matching the lot number on the packaging.

3 results found

Lot NumberCertificate TypeDateItem
G2223061Certificate of AnalysisApr 07, 2024 A110477
G2223062Certificate of AnalysisApr 07, 2024 A110477
G2223063Certificate of AnalysisApr 07, 2024 A110477

Chemical and Physical Properties

SolubilitySoluble in chloroform, ether, ethanol (~0.1 mg/ml), and DMF (~2 mg/ml). Insoluble in water.
Refractive Index1.425
Flash Point(°F)230 °F
Flash Point(°C)110 °C
Boil Point(°C)328°C
Melt Point(°C)74-77°C

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P271:Use only outdoors or in a well-ventilated area.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P403+P233:Store in a well-ventilated place. Keep container tightly closed.

P362+P364:Take off contaminated clothing and wash it before reuse.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P337+P317:If eye irritation persists: Get medical help.

P332+P317:If skin irritation occurs: Get medical help.

P319:Get medical help if you feel unwell.

RTECS JX3780000
Reaxy-Rn 1788211
Merck Index 764

Related Documents

Citations of This Product

1. Lei Jin, Ju Huang, Lei Guo, Bo Zhang, Qin Li, Hui Li, Mincheng Yu, Peiyi Xie, Qiang Yu, Zheng Chen, Shuang Liu, Yongfeng Xu, Yongsheng Xiao, Ming Lu, Qinghai Ye.  (2023)  CYP1B1 promotes colorectal cancer liver metastasis by enhancing the growth of metastatic cancer cells via a fatty acids-dependent manner.  Journal of Gastrointestinal Oncology,  14  (6): ( 2448–2465).  [PMID:38196537] [10.21037/jgo-23-895]
2. Ya Li, Chao-Yu Wang, Dong-Jin Qian.  (2023)  Interfacial self-assembly of Cd2+-tetraphenylethylene coordination polymers and their photophysical properties in Langmuir-Blodgett films.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,  673  (131741).  [PMID:] [10.1016/j.colsurfa.2023.131741]
3. 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).  [PMID:34517673] [10.1016/j.talanta.2021.122817]
4. Shuai Xiao, Hai-ou Li, Meng-wei Xu, Ke Huang, Zhou-fei Luo, Lang-tao Xiao.  (2021)  A high-throughput method for profiling fatty acids in plant seeds based on one-step acid-catalyzed methylation followed by gas chromatography-mass spectrometry.  BIOTECHNOLOGY & BIOTECHNOLOGICAL EQUIPMENT,      [PMID:] [10.1080/13102818.2021.1954552]
5. 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).  [PMID:33592752] [10.1016/j.talanta.2020.122022]
6. Mingzhu Yang, Binglei Song, Delun Du, Xiaomei Pei, Zhenggang Cui.  (2020)  Solution and emulsion behavior of highly soluble carboxylate surfactants with α-substituted phenoxy group.  JOURNAL OF MOLECULAR LIQUIDS,  299  (112130).  [PMID:] [10.1016/j.molliq.2019.112130]
7. Qi Zhao, Jian Li, Yang Xu, Dandan Lv, Kanyasiri Rakariyatham, Dayong Zhou.  (2019)  Rapid extraction of free fatty acids from edible oil after accelerated storage based on amino-modified magnetic silica nanospheres.  Analytical Methods,  11  (35): (4520-4527).  [PMID:] [10.1039/C9AY01082C]
8. Mingwei Zhao, Haonan He, Caili Dai, Xuepeng Wu, Yue Zhang, Yongping Huang, Chenglin Gu.  (2018)  Micelle formation by amine-based CO2-responsive surfactant of imidazoline type in an aqueous solution.  JOURNAL OF MOLECULAR LIQUIDS,  268  (875).  [PMID:] [10.1016/j.molliq.2018.08.010]
9. 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).  [PMID:29648434] [10.1021/acsami.8b00506]
10. Xi Chen, Nan Zheng, Qiao Wang, Lingzhi Liu, Yongfeng Men.  (2017)  Side-chain crystallization in alkyl-substituted cellulose esters and hydroxypropyl cellulose esters.  CARBOHYDRATE POLYMERS,  162  (28).  [PMID:28224891] [10.1016/j.carbpol.2017.01.028]
11. Yi Wang, Yu Zhang, TianDong Xia, WenJun Zhao, WeiHua Yang.  (2014)  Effects of fabricated technology on particle size distribution and thermal properties of stearic–eicosanoic acid/polymethylmethacrylate nanocapsules.  SOLAR ENERGY MATERIALS AND SOLAR CELLS,  120  (481).  [PMID:] [10.1016/j.solmat.2013.09.028]
12. Beibei Hu, Wei Sun, Haiting Li, Helin Sui, Sanming Li, .  (2018-06-23)  Systematic modifications of amino acid-based organogelators for the investigation of structure-property correlations in drug delivery system..  International journal of pharmaceutics,  547  ((1-2)): ( 637-647 ).  [PMID:29933060]
13. Beibei Hu,Wei Sun,Baixue Yang,Heran Li,Liuchenzi Zhou,Sanming Li.  (2018-05-31)  Application of Solvent Parameters for Predicting Organogel Formation..  AAPS PharmSciTech,  19  ((5)): (2288-2300).  [PMID:29845502]
14. Beibei Hu,Haipeng Yan,Yanping Sun,Xi Chen,Yujuan Sun,Sanming Li,Yongshuai Jing,Heran Li.  (2019-12-19)  Organogels based on amino acid derivatives and their optimization for drug release using response surface methodology..  Artificial cells, nanomedicine, and biotechnology,  48  ((1)): (266-275).  [PMID:31851842]

References

1. Lei Jin, Ju Huang, Lei Guo, Bo Zhang, Qin Li, Hui Li, Mincheng Yu, Peiyi Xie, Qiang Yu, Zheng Chen, Shuang Liu, Yongfeng Xu, Yongsheng Xiao, Ming Lu, Qinghai Ye.  (2023)  CYP1B1 promotes colorectal cancer liver metastasis by enhancing the growth of metastatic cancer cells via a fatty acids-dependent manner.  Journal of Gastrointestinal Oncology,  14  (6): ( 2448–2465).  [PMID:38196537] [10.21037/jgo-23-895]
2. Ya Li, Chao-Yu Wang, Dong-Jin Qian.  (2023)  Interfacial self-assembly of Cd2+-tetraphenylethylene coordination polymers and their photophysical properties in Langmuir-Blodgett films.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,  673  (131741).  [PMID:] [10.1016/j.colsurfa.2023.131741]
3. 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).  [PMID:34517673] [10.1016/j.talanta.2021.122817]
4. Shuai Xiao, Hai-ou Li, Meng-wei Xu, Ke Huang, Zhou-fei Luo, Lang-tao Xiao.  (2021)  A high-throughput method for profiling fatty acids in plant seeds based on one-step acid-catalyzed methylation followed by gas chromatography-mass spectrometry.  BIOTECHNOLOGY & BIOTECHNOLOGICAL EQUIPMENT,      [PMID:] [10.1080/13102818.2021.1954552]
5. 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).  [PMID:33592752] [10.1016/j.talanta.2020.122022]
6. Mingzhu Yang, Binglei Song, Delun Du, Xiaomei Pei, Zhenggang Cui.  (2020)  Solution and emulsion behavior of highly soluble carboxylate surfactants with α-substituted phenoxy group.  JOURNAL OF MOLECULAR LIQUIDS,  299  (112130).  [PMID:] [10.1016/j.molliq.2019.112130]
7. Qi Zhao, Jian Li, Yang Xu, Dandan Lv, Kanyasiri Rakariyatham, Dayong Zhou.  (2019)  Rapid extraction of free fatty acids from edible oil after accelerated storage based on amino-modified magnetic silica nanospheres.  Analytical Methods,  11  (35): (4520-4527).  [PMID:] [10.1039/C9AY01082C]
8. Mingwei Zhao, Haonan He, Caili Dai, Xuepeng Wu, Yue Zhang, Yongping Huang, Chenglin Gu.  (2018)  Micelle formation by amine-based CO2-responsive surfactant of imidazoline type in an aqueous solution.  JOURNAL OF MOLECULAR LIQUIDS,  268  (875).  [PMID:] [10.1016/j.molliq.2018.08.010]
9. 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).  [PMID:29648434] [10.1021/acsami.8b00506]
10. Xi Chen, Nan Zheng, Qiao Wang, Lingzhi Liu, Yongfeng Men.  (2017)  Side-chain crystallization in alkyl-substituted cellulose esters and hydroxypropyl cellulose esters.  CARBOHYDRATE POLYMERS,  162  (28).  [PMID:28224891] [10.1016/j.carbpol.2017.01.028]
11. Yi Wang, Yu Zhang, TianDong Xia, WenJun Zhao, WeiHua Yang.  (2014)  Effects of fabricated technology on particle size distribution and thermal properties of stearic–eicosanoic acid/polymethylmethacrylate nanocapsules.  SOLAR ENERGY MATERIALS AND SOLAR CELLS,  120  (481).  [PMID:] [10.1016/j.solmat.2013.09.028]
12. Beibei Hu, Wei Sun, Haiting Li, Helin Sui, Sanming Li, .  (2018-06-23)  Systematic modifications of amino acid-based organogelators for the investigation of structure-property correlations in drug delivery system..  International journal of pharmaceutics,  547  ((1-2)): ( 637-647 ).  [PMID:29933060]
13. Beibei Hu,Wei Sun,Baixue Yang,Heran Li,Liuchenzi Zhou,Sanming Li.  (2018-05-31)  Application of Solvent Parameters for Predicting Organogel Formation..  AAPS PharmSciTech,  19  ((5)): (2288-2300).  [PMID:29845502]
14. Beibei Hu,Haipeng Yan,Yanping Sun,Xi Chen,Yujuan Sun,Sanming Li,Yongshuai Jing,Heran Li.  (2019-12-19)  Organogels based on amino acid derivatives and their optimization for drug release using response surface methodology..  Artificial cells, nanomedicine, and biotechnology,  48  ((1)): (266-275).  [PMID:31851842]

Solution Calculators