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SML1395

Arachidonic acid sodium salt

from Mortierella alpina, ≥98.5% (GC), waxy solid, lipid precursor

Sinónimos:

5,8,11,14-Eicosatetraenoic acid, Eicosa-5Z,8Z,11Z,14Z-tetraenoic acid, Sodium arachidonate, cis,cis,cis,cis-5,8,11,14-Eicosatetraenoic acid sodium salt, 20:4

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Talla/SKUDisponibilidadPrecio
5 mg
Comprobar disponibilidad del carrito
$50.000
25 mg
Comprobar disponibilidad del carrito
$151.000
100 mg
Comprobar disponibilidad del carrito
$363.000

Acerca de este artículo

Fórmula empírica (notación de Hill):
C20H31O2Na
Número CAS:
Peso molecular:
326.45
UNSPSC Code:
12352211
PubChem Substance ID:
NACRES:
NA.77
Assay:
≥98.5% (GC)
Form:
waxy solid

$50.000


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Nombre del producto

Arachidonic acid sodium salt from Mortierella alpina, ≥98.5% (GC)

biological source

Mortierella alpina

Quality Segment

assay

≥98.5% (GC)

form

waxy solid

color

white to off-white

solubility

methanol: 50 mg/mL, clear, colorless to faintly yellow

shipped in

dry ice

storage temp.

−20°C

SMILES string

O=C(O[Na])CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC

InChI

1S/C20H32O2.Na/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22;/h6-7,9-10,12-13,15-16H,2-5,8,11,14,17-19H2,1H3,(H,21,22);/q;+1/p-1/b7-6-,10-9-,13-12-,16-15-;

InChI key

DDMGAAYEUNWXSI-XVSDJDOKSA-M

General description

Arachidonic acid (AA) is a polyunsaturated ϖ fatty acid constituent of the phospholipids of cell membranes. Structurally, it is a 20-carbon chain that contains four cis double bonds, which allow the free acid form of AA to be an insoluble oil; this can be converted to the water-soluble sodium salt form within the normal physiological pH range. Arachidonic acid is metabolized by multiple enzymes to yield various metabolites; AA and its metabolites play important roles in a variety of biological processes, including signal transduction, smooth muscle contraction, chemotaxis, cell proliferation and differentiation and apoptosis.

Application

Arachidonic acid is used in assays to measure activity of oxidizing enzymes, such as cyclooxygenase, as well as in assays to determine platelet inhibition in whole blood. Arachidonic acid has been demonstrated to bind to the a subunit of G protein and inhibit the activity of Ras GTPase-activating proteins (GAPs), to have a role in the development and progression of prostate cancer, and to enhance formation of lipid bodies in human mast cells.

Biochem/physiol Actions

Arachidonic acid (ARA) is a vital component of biological cell membranes, providing them with the necessary fluidity and flexibility crucial for the functioning of all cells, particularly in the nervous system, skeletal muscle, and immune system. Free ARA regulates the activity of ion channels, various receptors, and enzymes, both through activation and inhibition. ARA undergoes reacylation/deacylation cycles within cell membranes, maintaining its concentration at a low level and restricting its availability for oxidation. Metabolites resulting from ARA oxidation do not initiate inflammation but contribute to it, and more significantly, they generate mediators crucial for resolving inflammation and promoting wound healing. Released arachidonic acid (AA) reacts with molecular oxygen nonenzymatically, through oxidative stress, and enzymatically through the action of oxygenase enzymes. AA is oxidized to prostaglandins and thromboxanes by at least two cyclooxygenase (COX) isoforms, to leukotrienes and lipoxins by lipoxygenases, and to epoxyeicosatrienoic acids via cytochrome p450-catalyzed metabolism. Cellular uptake of arachidonic acid is energy-dependent and involves protein-facilitated transport across the plasma membrane.

Disclaimer

The sodium salts of arachidonic acid are very sensitive to oxidation and will turn yellow and deteriorate rapidly in air. They are packaged under vacuum in sealed ampules. Once opened the product must be used quickly or transferred into an inert atmosphere (dry argon) as soon as possible.

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181198900411E861810E
description

≥98.5% (GC)

description

Precursor for prostaglandins, prostacyclin, and thromboxane.

description

Avanti Research - A Croda Brand 900411E, ethanol solution

description

Avanti Research - A Croda Brand 861810E, ethanol solution

assay

≥98.5% (GC)

assay

≥99% (TLC and GC)

assay

>99% (TLC)

assay

>99% (TLC)

form

waxy solid

form

oil

form

ethanol solution

form

ethanol solution

Quality Level

200

Quality Level

100

Quality Level

-

Quality Level

-

storage temp.

−20°C

storage temp.

−70°C

storage temp.

−20°C

storage temp.

−70°C

solubility

methanol: 50 mg/mL, clear, colorless to faintly yellow

solubility

ethanol: 5 mg/mL

solubility

-

solubility

-

color

white to off-white

color

colorless

color

-

color

-


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Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup



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Questions

1–2 of 2 Questions  
  1. Can I dissolve the Arachidonic acid sodium salt (SML1395) in DMSO, rather than Methanol? If yes, does it retain the same potency in DMSO vs Methanol? Any information available on this?

    1 answer
    1. We only test this product for solubility in methanol and have no data regarding DMSO vs Methanol solubility. Doing a quick Google Search, this supplier states it is soluble in DMSO at 262.5 mg/mL. This is something you can investigate further.
      https://www.targetmol.com/compound/arachidonic%20acid

      Helpful?

  2. What is the tolerance range around -20C for the recommended storage temperature of SML1395

    1 answer
    1. The tolerance range for items assigned freezer storage at -20°C is -10 to -25°C.

      Helpful?

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