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67106

2-Linoleoylglycerol solution

~0.1 M in acetonitrile, analytical standard

Synonym(s):

β-Monolinolein, (9Z,12Z)-9,12-Octadecadienoic acid 2-hydroxy-1-(hydroxymethyl)ethyl ester, 2-Monolinolein, 2-Monolinoleoylglycerol

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About This Item

Empirical Formula (Hill Notation):
C21H38O4
CAS Number:
3443-82-1
Molecular Weight:
354.52
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
329760399
MDL number:
MFCD05863969
Beilstein/REAXYS Number:
1715064
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grade

analytical standard

assay

≥95.0% (GC)

form

liquid

shelf life

limited shelf life, expiry date on the label

concentration

~0.1 M in acetonitrile

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

food and beverages

format

single component solution

functional group

ester

storage temp.

−20°C

SMILES string

O=C(OC(CO)CO)CCCCCCC/C=C\C/C=C\CCCCC

InChI

1S/C21H38O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21(24)25-20(18-22)19-23/h6-7,9-10,20,22-23H,2-5,8,11-19H2,1H3/b7-6-,10-9-

InChI key

IEPGNWMPIFDNSD-HZJYTTRNSA-N

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

35.6 °F - closed cup

flash_point_c

2 °C - closed cup

Regulatory Information

危险化学品

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Certificates of Analysis (COA)

Lot/Batch Number
BCBT5897
BCBQ9767V

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Chia-Shan Wu et al.
PloS one, 8(4), e60314-e60314 (2013-04-09)
The G-protein coupled receptor 55 (GPR55) is activated by lysophosphatidylinositols and some cannabinoids. Recent studies found prominent roles for GPR55 in neuropathic/inflammatory pain, cancer and bone physiology. However, little is known about the role of GPR55 in CNS development and
Giuseppe Tortoriello et al.
PloS one, 8(7), e67865-e67865 (2013-07-23)
Lipid metabolism is critical to coordinate organ development and physiology in response to tissue-autonomous signals and environmental cues. Changes to the availability and signaling of lipid mediators can limit competitiveness, adaptation to environmental stressors, and augment pathological processes. Two classes
Caroline Turcotte et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 34(3), 4253-4265 (2020-02-06)
The endocannabinoid (eCB) 2-arachidonoyl-gycerol (2-AG) modulates immune responses by activating cannabinoid receptors or through its multiple metabolites, notably eicosanoids. Thus, 2-AG hydrolysis inhibition might represent an interesting anti-inflammatory strategy that would simultaneously increase the levels of 2-AG and decrease those
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Global Trade Item Number

SKUGTIN
505602000104055977243406