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ARACHIDONIC ACID SODIUM SALT

Product Name
ARACHIDONIC ACID SODIUM SALT
CAS No.
6610-25-9
Chemical Name
ARACHIDONIC ACID SODIUM SALT
Synonyms
SODIUM ARACHIDONATE;Arachidonicacidsodiumsal;ARACHIDONIC ACID SODIUM SALT;5Z,8Z,11Z,14Z-EICOSATETRAENOIC;5,8,11,14-EICOSATETRAENOIC ACID;Arachidonic acid sodium salt from;EICOSA-5Z,8Z,11Z,14Z-TETRAENOIC ACID;ARACHIDONIC ACID SODIUM FROM PORCINELIVE R;5,8,11,14-EICOSATETRAENOIC ACID SODIUM SALT;ARACHIDONIC ACID, PORCINE LIVER, SODIUM SALT
CBNumber
CB0461041
Molecular Formula
C20H31NaO2
Formula Weight
326.45
MOL File
6610-25-9.mol
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ARACHIDONIC ACID SODIUM SALT Property

Flash point:
113℃
storage temp. 
-20°C
solubility 
methanol: 50 mg/mL, clear, colorless to faintly yellow
form 
waxy solid
color 
white to off-white
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Safety

Risk Statements 
19
WGK Germany 
3
RTECS 
JX3874000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P312Call a POISON CENTER or doctor/physician if you feel unwell.

P362Take off contaminated clothing and wash before reuse.

P403+P233Store in a well-ventilated place. Keep container tightly closed.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SML1395
Product name
Arachidonic acid sodium salt from
Purity
≥98.5% (GC)
Packaging
5mg
Price
$46.5
Updated
2024/03/01
Sigma-Aldrich
Product number
SML1395
Product name
Arachidonic acid sodium salt from
Purity
≥98.5% (GC)
Packaging
25mg
Price
$180
Updated
2024/03/01
Sigma-Aldrich
Product number
5.32830
Product name
Arachidonic Acid, Fungal sp., Sodium Salt - CAS 6610-25-9 - Calbiochem
Purity
Precursor for prostaglandins, prostacyclin, and thromboxane.
Packaging
100MG
Price
$242
Updated
2022/05/15
Cayman Chemical
Product number
10006607
Product name
Arachidonic Acid (sodium salt)
Purity
≥98%
Packaging
25mg
Price
$50
Updated
2024/03/01
Cayman Chemical
Product number
10006607
Product name
Arachidonic Acid (sodium salt)
Purity
≥98%
Packaging
50mg
Price
$94
Updated
2024/03/01
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ARACHIDONIC ACID SODIUM SALT Chemical Properties,Usage,Production

Uses

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.

General Description

Arachidonic acid (AA) is a polyunsaturated ? 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.

Biochem/physiol Actions

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.

ARACHIDONIC ACID SODIUM SALT Preparation Products And Raw materials

Raw materials

Preparation Products

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6610-25-9, ARACHIDONIC ACID SODIUM SALTRelated Search:


  • EICOSA-5Z,8Z,11Z,14Z-TETRAENOIC ACID
  • CIS,CIS,CIS,CIS-5,8,11, 14-EICOSATETRAENOIC ACID, NA
  • CIS,CIS,CIS,CIS-5,8,11,14-EICOSATETRAENOIC ACID SODIUM SALT
  • ARACHIDONIC ACID SODIUM SALT
  • ARACHIDONIC ACID, PORCINE LIVER, SODIUM SALT
  • 5Z,8Z,11Z,14Z-EICOSATETRAENOIC ACID, SODIUM SALT
  • 5,8,11,14-EICOSATETRAENOIC ACID
  • 5,8,11,14-EICOSATETRAENOIC ACID SODIUM SALT
  • SODIUM ARACHIDONATE
  • 11,14-eicosatetraenoicacid,sodiumsalt,(all-z)-8
  • ARACHIDONIC ACID SODIUM FROM PORCINELIVE R
  • ARACHIDONIC ACID SODIUM SALT, FROM PORCINE LIVER
  • (5Z,8Z,11Z,14Z)-5,8,11,14-Icosatetraenoic acid sodium salt
  • 5Z,8Z,11Z,14Z-EICOSATETRAENOIC
  • Arachidonic acid sodium salt from
  • sodium:(5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoate
  • Arachidonic acid sodium salt from Mortierella alpina
  • Arachidonic acid sodium salt,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
  • Arachidonic acid sodium salt from Mortierella alpina >=98.5% (GC)
  • Arachidonicacidsodiumsal
  • 6610-25-9
  • C20H31NaO2
  • C20H31O2Na
  • BioChemical
  • Biochemicals and Reagents
  • Fatty Acids
  • Lipids
  • Polyunsaturated
  • Omega 6 fatty acids and derivatives
  • Unsaturated fatty acids and derivatives