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860202C

Avanti

16:0 Phosphatidylbutanol

1,2-dipalmitoyl-sn-glycero-3-phosphobutanol (sodium salt), chloroform

Synonym(s):

1,2-dihexadecanoyl-sn-glycero-3-phosphobutanol (sodium salt)

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About This Item

Empirical Formula (Hill Notation):
C39H76O8PNa
CAS Number:
92609-92-2
Molecular Weight:
726.98
UNSPSC Code:
12352211
NACRES:
NA.25

Assay

>99% (TLC)

form

liquid

packaging

pkg of 1 × 2.5 mL (860202C-25mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 860202C

concentration

10 mg/mL (860202C-25mg)

shipped in

dry ice

storage temp.

−20°C

InChI

1S/C39H77O8P.Na/c1-4-7-10-12-14-16-18-20-22-24-26-28-30-32-38(40)44-35-37(36-46-48(42,43)45-34-9-6-3)47-39(41)33-31-29-27-25-23-21-19-17-15-13-11-8-5-2;/h37H,4-36H2,1-3H3,(H,42,43);/q;+1/p-1/t37-;/m1./s1

InChI key

CZFXRJUSZGHONR-GKEJWYBXSA-M

General description

Phosphatidylbutanol is a low polarity phospholipid, which can be produced by phospholipase D (PLD) specific transphosphatidylation reaction of phosphatidylcholine (PC) and butanol.

Application

16:0 Phosphatidylbutanol or 1,2-dipalmitoyl-sn-glycero-3-phosphobutanol (sodium salt) has been used to analyze the in vivo activity of phospholipase D (PLD) in Taxus cuspidate using liquid chromatography electrospray ionization tandem mass spectrometric (LC/ESI-MS/MS).

Biochem/physiol Actions

Phosphatidylbutanol is used as a biomarker in phospholipase D activity assays.

Packaging

5 mL Clear Glass Sealed Ampule (860202C-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

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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Song Yang et al.
Biochimica et biophysica acta, 1771(5), 600-612 (2007-04-13)
A comparative lipidomics approach was employed to investigate the changes in membrane phospholipids during the procession of cellular development and apoptosis of two plant cell lines, Taxus cuspidata and Taxus chinensis var. mairei. Analysis of lipids by LC/ESI/MS(n) showed more
Song Yang et al.
Chemistry and physics of lipids, 159(1), 13-20 (2009-05-12)
Degradation of membrane phospholipids is associated with apoptotic responses, but the signaling development of this degradation is not well understood. Cerium (Ce(4+)), an important rare earth element, induces cellular apoptosis and taxol biosynthesis in Taxus cuspidata suspension cultures. Here, using
Pei-pei Han et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 23(2), 623-630 (2008-10-17)
Lipid signaling involved in mechanotransduction processes in response to shear stress in plants remained elusive. To understand the responses of phospholipids in shear stress-induced mechanotransduction, a lipidomic approach was employed to profile phospholipid species of Taxus cuspidata cells under laminar
Mikhail Vyssotski et al.
Lipids, 44(4), 381-389 (2008-12-17)
High-performance TLC and (31)P-NMR were assessed as methods of observing the presence of numerous low polarity phospholipids: bis-phosphatidic acid (BPA), semi-lyso bis-phosphatidic acid (SLBPA), N-acyl phosphatidylethanolamine (NAPE), N-(1,1-dimethyl-3-oxo-butyl)-phosphatidylethanolamine (diacetone adduct of PE, DOBPE), N-acetyl PE, phosphatidylmethanol (PM), phosphatidylethanol (PEt), phosphatidyl-n-propanol

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