Acido arachidico - standard analitico , CAS No.506-30-9

CAS: 506-30-9 Cat. No.: A110477 Formula: C₂₀H₄₀O₂ Peso molecolare: 312.53 Beilstein Registry Number: 1788211 Numero EC: 208-031-3

QUALITÀ & PUREZZA Analytical standard, Moligand™

Synonyms

fatty acid 20:0|Elcosanoic Acid|C20:0|ARACHIDIC ACID [MI]|CH3-[CH2]18-COOH|n-Eicosanoic acid|eicosatrienoic-acid|Arachidic acid|ARACHIDIC ACID (CONSTITUENT OF BORAGE SEED OIL)|Arachinsaeure|CH3-(CH2)18-COOH|Icosanoicacid|ARACHIDIC ACID [INCI]|eicosanoate|Arachic acid|FA 20:0|EICOSANOIC ACID|Arachate|Icosanoic acid|Arachidic acid (synthetic)|Arachidinic acid|Eicosanoicacid

Storage

Conservare a -20°C

Shipped In

Cassetta del ghiaccio + cuscini per il ghiaccio

Panoramica

È un acido grasso saturo che si trova naturalmente negli oli di pesce e vegetali e può essere formato anche dall'idrogenazione dell'acido arachidonico. Le diete ricche di acidi grassi saturi, come l'acido arachidico, sono note per l'aumento delle lipoproteine a bassa densità nel siero, con conseguenti livelli elevati di colesterolo nel sangue. Per le sue proprietà tensioattive, l'acido arachidico è utilizzato nella produzione di prodotti farmaceutici, saponi, cosmetici e imballaggi alimentari.
Un acido grasso saturo.

Specifiche

Sinonimi

fatty acid 20:0 | Elcosanoic Acid | C20:0 | ARACHIDIC ACID [MI] | CH3-[CH2]18-COOH | n-Eicosanoic acid | eicosatrienoic-acid | Arachidic acid | ARACHIDIC ACID (CONSTITUENT OF BORAGE SEED OIL) | Arachinsaeure | CH3-(CH2)18-COOH | Icosanoicacid | ARACHIDIC ACID [INCI] | eicosanoate | Arachic acid | FA 20:0 | EICOSANOIC ACID | Arachate | Ico Mostra altro

Specifiche e purezza

standard analitico

Condizioni di conservazione di stoccaggio

Conservare a -20°C

Spedito in

Cassetta del ghiaccio + cuscini per il ghiaccio

Grado

Moligand™, Standard analitico

Nomi e identificatori

Pubchem Sid

528775137

Sorrisi canonici

CCCCCCCCCCCCCCCCCCCC(=O)O

IUPAC Name

icosanoic acid

InChIKey

VKOBVWXKNCXXDE-UHFFFAOYSA-N

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)

Isomeri SMILES

CCCCCCCCCCCCCCCCCCCC(=O)O

RTECS

JX3780000

Peso molecolare

312.53

Beilstein

1788211

Reaxy-Rn

1788211

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1788211&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Classe Fatty Acyls
      • Subclass Fatty acids and conjugates

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: Fatty Acyls
• Subclass: Fatty acids and conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: 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: 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
• Descrizione: This compound belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 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.

DOI: 10.1186/s13321-016-0174-y

Obiettivi associati (umani)

ACHE Tclin Acetylcholinesterase (18204 Activities)

Discover Target: ACHE

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

PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)

Discover Target: PPARG

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

PPARA Tclin Peroxisome proliferator-activated receptor alpha (9197 Activities)

Discover Target: PPARA

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

Obiettivi associati (non umani)

Ppard Peroxisome proliferator-activated receptor delta (358 Activities)

Discover Target: Ppard

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

Ptpn1 Protein-tyrosine phosphatase 1B (270 Activities)

Discover Target: Ptpn1

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

Trpv2 Transient receptor potential cation channel subfamily V member 2 (148 Activities)

Discover Target: Trpv2

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in chloroform, ether, ethanol (~0.1 mg/ml), and DMF (~2 mg/ml). Insoluble in water.
• Indice di rifrazione: 1.425
• Punto di infiammabilità (°F): 230 °F
• Punto di infiammabilità (°C): 110 °C
• Punto di ebollizione (°C): 328°C
• Punto di fusione (°C): 74-77°C
• Peso molecolare: 312.500 g/mol
• XLogP3: 8.500
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 18
• Exact Mass: 312.303 Da
• Monoisotopic Mass: 312.303 Da
• Topological Polar Surface Area: 37.300 Ų
• Heavy Atom Count: 22
• Formal Charge: 0
• Complexity: 226.000
• 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