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ChemicalBook > Product Catalogue >Analytical Chemistry >Standard >Analytical Standards >2-MONOPALMITIN

2-MONOPALMITIN

2-MONOPALMITIN Structure
  • ₹32226.03
  • Product name: 2-MONOPALMITIN
  • CAS: 23470-00-0
  • MF: C19H38O4
  • MW: 330.5
  • EINECS:
  • MDL Number:MFCD00058513
  • Synonyms:2-monopalmitoylglycerol (C16:0);2-O-Hexadecanoylglycerol;2-O-Palmitoylglycerol;2-O-Palmitoyl-L-glycerol;Hexadecanoic acid [2-hydroxy-1-(hydroxymethyl)ethyl] ester;Palmitic acid 2-hydroxy-1-(hydroxymethyl)ethyl ester;2-(1,3-dihydroxypropan-2-yl)hexadecanoic acid compound with 1,3-dihydroxypropan-2-yl palmitate (1:1);2-Hexadecanoylglycerol
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Brand

  • Sigma-Aldrich(India)

Package

  • 25MG
  • ManufacturerSigma-Aldrich(India)
  • Product number75614
  • Product description2-Palmitoylglycerol analytical standard
  • Packaging25MG
  • Price₹32226.03
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) 75614 2-Palmitoylglycerol analytical standard 25MG ₹32226.03 2022-06-14 Buy

Properties

Melting point :68-70°C
Boiling point :387.92°C (rough estimate)
Density :0.9708 (rough estimate)
refractive index :1.4434 (estimate)
storage temp. :−20°C
solubility :Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
pka :13.54±0.10(Predicted)
form :Solid
color :White to Off-White
BRN :1796692

Safety Information

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Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
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Description

2-Arachidonoyl glycerol (2-AG; ) is an endogenous agonist of the CB1 and CB2 cannabinoid receptors. 2-Palmitoyl glycerol is a fatty acid ester that does not bind directly to cannabinoid receptors, nor inhibit adenylyl cyclase, but rather potentiates the activity of 2-AG (and other endocannabinoids) to bind to CB1 and CB2 and inhibit adenylyl cyclase. This “entourage” effect has been attributed to blockade of the breakdown and reuptake pathways that normally function to reduce endocannabinoid levels rapidly upon release. 2-Palmitoyl glycerol and related endogenous fatty acid derivatives have been shown to interact with endocannabinoids in the modulation of pain sensitivity.

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