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860777C

Avanti

18:0 Dibromo MG

Avanti Research™ - A Croda Brand 860777C

Synonym(s):

1-(9,10-dibromostearoyl)-rac-glycerol

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About This Item

Empirical Formula (Hill Notation):
C21H40Br2O4
CAS Number:
1438282-43-9
Molecular Weight:
516.35
UNSPSC Code:
12352211
NACRES:
NA.25

form

liquid

packaging

pkg of 1 × 2.5 mL (860777C-25mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 860777C

concentration

10 mg/mL (860777C-25mg)

shipped in

dry ice

storage temp.

−20°C

SMILES string

OCC([H])(O)COC(CCCCCCCC(Br)C(Br)CCCCCCCC)=O

General description

18:0 Dibromo MG, also known as 1-(9,10-dibromostearoyl)-rac-glycerol, is a detergent. It is widely used in lipid mesophase crystallization.

Packaging

5 mL Clear Glass Sealed Ampule (860777C-25mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

Target Organs

Central nervous system

WGK

WGK 3

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Agnieszka U Blachnio-Zabielska et al.
Rapid communications in mass spectrometry : RCM, 25(15), 2223-2230 (2011-07-08)
Long-chain acyl-coenzymes A (acyl-CoAs) (LCACoA) are the activated forms of long-chain fatty acids and serve as key lipid metabolites. Excess accumulation of intracellular LCACoA, diacylglycerols (DAGs) and ceramides may create insulin resistance with respect to glucose metabolism. We present a
Evgeny V Berdyshev et al.
The Journal of biological chemistry, 284(9), 5467-5477 (2009-01-03)
Novel immunomodulatory molecule FTY720 is a synthetic analog of myriocin, but unlike myriocin FTY720 does not inhibit serine palmitoyltransferase. Although many of the effects of FTY720 are ascribed to its phosphorylation and subsequent sphingosine 1-phosphate (S1P)-like action through S1P(1,3-5) receptors

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