Skip to Content
Merck
All Photos(1)

Documents

870282C

Avanti

18:1 Biotinyl PE

Avanti Research™ - A Croda Brand 870282C

Synonym(s):

1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-N-(biotinyl) (sodium salt)

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C51H91N3O10PNaS
CAS Number:
384835-53-4
Molecular Weight:
992.31
UNSPSC Code:
12352211
NACRES:
NA.25

form

liquid

packaging

pkg of 1 × 2.5 mL (870282C-25mg)
pkg of 1 × 4 mL (870282C-100mg)
pkg of 2 × 4 mL (870282C-200mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 870282C

concentration

10 mg/mL (870282C-25mg)
25 mg/mL (870282C-100mg)
25 mg/mL (870282C-200mg)

shipped in

dry ice

storage temp.

−20°C

SMILES string

[H][C@@](COP([O-])(OCCN([H])C(CCCC[C@](SC[C@@]1(NC(N2)=O)[H])([C@]12[H])[H])=O)=O)(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCC/C=C\CCCCCCCC)=O.[Na+]

InChI

1S/C51H92N3O10PS.Na/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-37-48(56)61-41-44(64-49(57)38-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2)42-63-65(59,60)62-40-39-52-47(55)36-34-33-35-46-50-45(43-66-46)53-51(58)54-50;/h17-20,44-46,50H,3-16,21-43H2,1-2H3,(H,52,55)(H,59,60)(H2,53,54,58);/q;+1/p-1/b19-17-,20-18-;/t44-,45+,46+,50+;/m1./s1

InChI key

ZGFSYDGJPSEMJM-AOAFAMOJSA-M

General description

18:1 Biotinyl PE, also referred as 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-N-(biotinyl), belongs to a class of head group modified functionalized lipids.

Application

18:1 Biotinyl PE is suitable: to tag N-glycolyl-monosialodihexosyl-ganglioside (NGcGM3) in the competitive assay, in preparation of small unilamellar vesicle, to test the functionalization of Polydimethylsiloxane (PDMS) polymer.

Packaging

5 mL Clear Glass Sealed Ampule (870282C-100mg)
5 mL Clear Glass Sealed Ampule (870282C-200mg)
5 mL Clear Glass Sealed Ampule (870282C-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 - Aquatic Chronic 3 - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

Target Organs

Central nervous system, Liver,Kidney

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

does not flash

Flash Point(C)

does not flash

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

H Zhan
Journal of biochemical and biophysical methods, 41(1), 13-19 (1999-10-08)
A general method for measuring interaction of liposome-protein (or potentially small molecules) was developed. This method utilizes biotinylated liposomes to incubate with interactants. Streptavidin-coated paramagnetic resins were then added and the liposomes (along with bound materials) can be quickly separated
Bo Huang et al.
Lab on a chip, 6(3), 369-373 (2006-03-03)
Polydimethylsiloxane (PDMS) surfaces can be functionalized with biotin groups by adding biotinylated phospholipids to the PDMS prepolymer before curing. The addition of beta-D-dodecyl-N-maltoside (DDM) in the solution blocks non-specific protein binding on these functionalized PDMS surfaces. We characterize the surface
M Virginia Gentilini et al.
Cancer immunology, immunotherapy : CII, 65(5), 551-562 (2016-03-13)
The expression of N-glycolyl-monosialodihexosyl-ganglioside (NGcGM3) in humans is restricted to cancer cells; therefore, it is a tumor antigen. There are measurable quantities of circulating anti-NGcGM3 antibodies (aNGcGM3 Abs) in human serum. Interestingly, some people have circulating Ag-specific immunoglobulins G (IgGs)
Ingrid Albertsson et al.
Scientific reports, 9(1), 17234-17234 (2019-11-23)
Denitrification is a microbial pathway that constitutes an important part of the nitrogen cycle on earth. Denitrifying organisms use nitrate as a terminal electron acceptor and reduce it stepwise to nitrogen gas, a process that produces the toxic nitric oxide
Heun Jin Lee et al.
Proceedings of the National Academy of Sciences of the United States of America, 105(49), 19253-19257 (2008-12-03)
Recent advances have enabled 3-dimensional reconstructions of biological structures in vivo, ranging in size and complexity from single proteins to multicellular structures. In particular, tomography and confocal microscopy have been exploited to capture detailed 3-dimensional conformations of membranes in cellular
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service