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Merck
CN

850483C

Avanti

18:1 Cyanine 5 PC

Avanti Research™ - A Croda Brand

Synonym(s):

1,2-dioleoyl-sn-glycero-3-phosphocholine-N-(Cyanine 5)

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About This Item

Empirical Formula (Hill Notation):
C77H124ClN4O9P
CAS Number:
2342573-49-1
Molecular Weight:
1316.26
UNSPSC Code:
12352211
NACRES:
NA.25

Key Documents

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Product Name

18:1 Cyanine 5 PC, Avanti Research™ - A Croda Brand

InChI

1S/C77H123N4O9P.ClH/c1-10-12-14-16-18-20-22-24-26-28-30-32-34-36-43-57-74(83)87-64-66(90-75(84)58-44-37-35-33-31-29-27-25-23-21-19-17-15-13-11-2)65-89-91(85,86)88-63-62-81(8,9)61-59-78-73(82)56-42-39-49-60-80-70-53-48-46-51-68(70)77(5,6)72(80)55-41-38-40-

InChI key

FRDSIEVJUUFAKX-IEXYBMNJSA-N

SMILES string

[H][C@@](COP([O-])(OCC[N+](C)(CCNC(CCCCC[N+]1=C(/C=C/C=C/C=C2C(C)(C)C(C=CC=C3)=C3N\2C)C(C)(C)C4=C1C=CC=C4)=O)C)=O)(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCC/C=C\CCCCCCCC)=O.[Cl-]

assay

99% (TLC)

form

solution

packaging

package of 1 × 250 μg

manufacturer/tradename

Avanti Research™ - A Croda Brand

concentration

1 mg/mL in chloroform

lipid type

fluorescent lipids

shipped in

dry ice

storage temp.

−20°C

Packaging

5 mL Clear Glass Sealed Ampule (850483C-250ug)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

signalword

Danger

Hazard Classifications

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

target_organs

Liver,Kidney, Respiratory system

Storage Class

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

危险化学品
易制毒化学品（2类）
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Naomi Benne et al.
Advanced healthcare materials, 9(10), e2000043-e2000043 (2020-04-25)
Atherosclerosis is characterized by the retention of lipids in foam cells in the arterial intima. The liver X receptor (LXR) agonist GW3965 is a promising therapeutic compound, since it induces reverse cholesterol transport in foam cells. However, hepatic LXR activation

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