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PHOSPHATIDYLETHANOLAMINE

Product Name
PHOSPHATIDYLETHANOLAMINE
CAS No.
39382-08-6
Chemical Name
PHOSPHATIDYLETHANOLAMINE
Synonyms
Cephalins;L-A-PHOSPHATIDYLETHANOLAMINE TYPE III:*F ROM EGG YOL;1,2-Diacyl-sn-glycero-3-phosphoethanolamine, L-α-Cephalin;1,2-Diacyl-sn-glycero-3-phosphoethanolamine, 3-sn-Phosphatidylethanolamine, L-α-Cephalin;Kephalins;E COLI PE;Cephalinex;PE/Cephalin;l-α-cephalin;Phospholipids cephalins
CBNumber
CB7198531
Molecular Formula
C41H78NO8P
Formula Weight
744.033681
MOL File
39382-08-6.mol
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PHOSPHATIDYLETHANOLAMINE Property

Density 
approximate 1.47g/ml(20℃)
storage temp. 
-20°C
solubility 
chloroform: 50 mg/mL, slightly hazy, brown-yellow
form 
solution
color 
Off-white to light yellow
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Safety

Hazard Codes 
Xn
Risk Statements 
22-38-40-48/20/22-67-36/38-20-63-68/20/21/22-20/21/22-20/22
Safety Statements 
36/37-26
RIDADR 
UN 1888 6.1/PG 3
WGK Germany 
3
1-8-10
HS Code 
2923202000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H331Toxic if inhaled

H336May cause drowsiness or dizziness

H351Suspected of causing cancer

H372Causes damage to organs through prolonged or repeated exposure

H412Harmful to aquatic life with long lasting effects

Precautionary statements

P201Obtain special instructions before use.

P273Avoid release to the environment.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P308+P313IF exposed or concerned: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
1535744
Product name
Phosphatidylethanolamine
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
100mg
Price
$805
Updated
2024/03/01
Sigma-Aldrich
Product number
60660
Product name
3-sn-Phosphatidylethanolamine solution
Purity
≥97.0% (10 mg phospholipid per ml CHCl3, TLC)
Packaging
1ml
Price
$120
Updated
2023/06/20
Cayman Chemical
Product number
24332
Product name
Phosphatidylethanolamines (egg)
Purity
≥98%
Packaging
50mg
Price
$305
Updated
2024/03/01
Cayman Chemical
Product number
24332
Product name
Phosphatidylethanolamines (egg)
Purity
≥98%
Packaging
100mg
Price
$578
Updated
2024/03/01
Sigma-Aldrich
Product number
Y0001953
Product name
Phosphatidylethanolamine from soya bean
Purity
European Pharmacopoeia (EP) Reference Standard
Packaging
y0001953
Price
$156
Updated
2024/03/01
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PHOSPHATIDYLETHANOLAMINE Chemical Properties,Usage,Production

Uses

L-α-Phosphatidylethanolamine from egg yolk has been used:

  • as a component of lipid mixture for the synthesis of giant unilamellar vesicles (GUVs)
  • in ceramide phosphoethanolamine (CPE) synthase assay using crude sphingomyelin synthase-related protein from Hela cells
  • for the standard curve generation for the quantification of lipids in plantaris muscle homogenates from mice

General Description

L-α-Phosphatidylethanolamine from egg yolk has high unsaturated fatty acid content and elicits radical-scavenging activity. L-α-Phosphatidylethanolamine (PE) is a membrane phospholipid and is interconverted to phosphotidylserine in the presence of phosphatidylserine synthase 2. PE is essential for maintaining the structural integrity of membranes. It is the second most abundant phospholipid in animals, plants and yeast and the major lipid in bacteria. It is synthesized in mitochondria in mammals.

Enzyme inhibitor

This hygroscopic phospholipid, also called cephalin and 1,2-diacyl-snglycero- 3-phosphoethanolamine, is an important constituent of biomembranes and lipoproteins. It is the major structural phospholipid in brain tissue. The physical properties depend on the nature of the acyl groups and on the presence of other lipids. Freshly prepared phosphatidylethanolamines are white solids that turn yellow and brown on exposure to air. They typically sinter between 80 and 90°C and melt in the neighborhood of 175°C. Solutions of phosphatidylethanolamine slowly decompose at room temperature (roughly 0.3-0.5% per day); hence, solutions should always be freshly prepared and kept cold prior to use. It is labile in alkaline conditions. See also specific compound Target(s): b- N-acetylglucosaminyl-glycopeptide b-1,4-galactosyltransferase; Nacetyllactosamine synthase; acylglycerol kinase, or monoacylglycerol kinase; cholesterol monooxygenase, side-chain-cleaving, or CYP11A1; chymase; cytidylate cyclase; dolichyldiphosphatase; dolichyl-phosphatase; dopamine b-monooxygenase; ethanolaminephosphotransferase; glutamate dehydrogenase; γ-glutamyl transpeptidase, mildly inhibited; glycerol-3-phosphate Oacyltransferase; glycerone-phosphate O-acyltransferase, or dihydroxyacetione-phosphate O-acyltransferase; hormone-sensitive lipase; 3-hydroxybutyrate dehydrogenase; indole-3-acetate b-glucosyltransferase; phosphatidate cytidylyltransferase; 1- phosphatidylinositol 4-kinase; phosphoinositide phospholipase C; phospholipase D, phosphatidylcholine-specific enzyme; sphingomyelin phosphodiesterase; steryl-b-glucosidase; UDP-Nacetylglucosamine: dolichyl-phosphate N-acetylglucosaminephosphotransferase.

Purification Methods

Purify the cephalin by dissolving it in EtOH, adding Pb(OAc)2.3H3O (30g in 100mL H2O) until excess Pb2+ is present. Filter off the solid. Pass CO2 gas through the solution until precipitation of PbCO3 ceases. Filter the solid off and evaporate (while bubbling CO2) under vacuum. An equal volume of H2O is added to the residual oil and extracted with hexane. The hexane extract is washed with H2O until the aqueous phase is free from Pb [test with dithizone (2 mg in 100 mL CCl4; Feigel Spot Tests Vol I, Elsevier p. 10 1954)]. The hexane is dried (Na2SO4), filtered and evaporated to give a yellow waxy solid which should be dried to constant weight in vacuo. It is practically insoluble in H2O and Me2CO, but freely soluble in CHCl3 (5%) and Et2O, and slightly soluble in EtOH. [Schofield & Dutton Biochemical Preparations 5 5 1957.]

PHOSPHATIDYLETHANOLAMINE Preparation Products And Raw materials

Raw materials

Preparation Products

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PHOSPHATIDYLETHANOLAMINE Suppliers

Alfa Chemistry
Tel
1-516-6625404
Fax
1-516-927-0118
Email
support@alfa-chemistry.com
Country
United States
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9171
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TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
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32161
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Alfa Chemistry
Tel
Fax
1-516-927-0118
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Info@alfa-chemistry.com
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Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
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58
Cayman Chemical Company
Tel
--
Fax
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Email
cayman@caymanchem.com
Country
United States
ProdList
6213
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81
Riedel-de Haen AG
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United States
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6773
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INDOFINE Chemical Company, Inc.
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chemical@indofinechemical.com
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United States
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Avanti Polar Lipids, Inc.
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info@avantilipids.com
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United States
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39382-08-6, PHOSPHATIDYLETHANOLAMINERelated Search:


  • 1,2-Diacyl-sn-glycero-3-phosphoethanolamine, L-α-Cephalin
  • 1,2-Diacyl-sn-glycero-3-phosphoethanolamine, 3-sn-Phosphatidylethanolamine, L-α-Cephalin
  • [(2R)-1-[2-azanylethoxy(hydroxy)phosphoryl]oxy-3-pentadecanoyloxy-propan-2-yl] icosanoate
  • arachidic acid [(1R)-1-[[2-aminoethoxy(hydroxy)phosphoryl]oxymethyl]-2-pentadecanoyloxy-ethyl] ester
  • PHOSPHATIDYLCHOLINE(EGG)(RG)
  • 3-sn-Phosphatidylethanolamine solution,L-α-Cephalin
  • L-α-Phosphatidylethanolamine from egg yolk,1,2-Diacyl-sn-glycero-3-phosphoethanolamine, L-α-Cephalin
  • L-α-Phosphatidylethanolamine from Escherichia coli,1,2-Diacyl-sn-glycero-3-phosphoethanolamine, 3-sn-Phosphatidylethanolamine, L-α-Cephalin
  • L-α-Phosphatidylethanolamine from Glycine max (soybean),1,2-Diacyl-sn-glycero-3-phosphoethanolamine, L-α-Cephalin
  • 3-SN-PHOSPHATIDYLETHANOLAMINE E COLI
  • Cephalins
  • L-A-PHOSPHATIDYLETHANOLAMINE TYPE V-A
  • L-A-PHOSPHATIDYLETHANOLAMINE TYPE III:*F ROM EGG YOL
  • L-A-PHOSPHATIDYLETHANOLAMINE TYPE V*FROM ESCHERICHI
  • 3-SN-PHOSPHATIDYLETHANOLAMINE SOLUTION, FROM SOYBEAN
  • 3-SN-PHOSPHATIDYLETHANOLAMINE FROM E. CO LI
  • L-A-PHOSPHATIDYLETHANOLAMINE TYPE III
  • L-A-PHOSPHATIDYLETHANOLAMINE TYPE IX*FRO M ESCHERICH
  • L-A-PHOSPHATIDYLETHANOLAMINE TYPE IV:*FR OM SOYBEAN
  • L-A-PHOSPHATIDYLETHANOLAMINE*TYPE VII-A FROM BOVINE
  • L-A-PHOSPHATIDYLETHANOLAMINE TYPE VII:*F ROM BOVINE
  • L-A-PHOSPHATIDYLETHANOLAMINE TYPE VII*FR OM BOVINE L
  • 3-SN-PHOSPHATIDYLETHANOLAMINE SOLUTION, FROM EGG YOLK
  • L-A-PHOSPHATIDYLETHANOLAMINE TYPE III*FR OM EGG YOLK
  • PhosphatidylethanolamineExEgg
  • l-α-cephalin
  • l-α-phosphatidylethanolamine from egg yolk
  • l-α-phosphatidylethanolamine from escherichia coli
  • l-α-phosphatidylethanolamine from glycine max (soybean)
  • L-ALPHA-PHOSPHATIDYLETHANOLAMINE SOLUTION, EGG YOLK
  • Phosphatidylethanolamine (100 mg) (COLD SHIPMENT REQUIRED)
  • L-LPHA-PHOSPHATIDYLETHANOLAMINE FRO
  • L-A-PHOSPHATIDYLETHANOLAMINE TYPE IV
  • 3-sn-phosphatidylethanolaminesolution
  • PHOSPHATIDYLETHANOLAMINE
  • Phosphatidylethanolamine (100 mg) (INTERNATIONAL COLD CHAIN SHIPMENT REQUIRED)
  • Cephalinex
  • Glycerophospholipids cephalins
  • Kephalins
  • Phospholipids cephalins
  • L-3-PHOSPHATIDYLETHANOLAMINE
  • L-ALPHA-CEPHALIN E COLI
  • L-ALPHA-CEPHALIN TYPE V ESCHERICHIA COLI
  • L-ALPHA-PHOSPHATIDYLETHANOLAMINE TYPE V ESCHERICHIA COLI
  • L-A-PHOSPHATIDYLETHANOLAMINE (E COLI)
  • E COLI PE
  • 1,2-DIACYL-SN-GLYCERO-3-PHOSPHOETHANOLAMINE TYPE V ESCHERICHIA COLI
  • L-alpha-Phosphatidylethanolamine from Glycine max (soybean)
  • L-alpha-Phosphatidylethanolamine from egg yolk
  • Phosphatidylethanolamine from soya bean
  • PHOSPHATIDYLETHANOLAMINE (PE)
  • (18R,21S)-24-Amino-21-hydroxy-21-oxido-15-oxo-16,20,22-trioxa-21λsup5sup-phosphatetracosan-18-ylicosanoate
  • PHOSPHATIDYLETHANOLAMINE ISO 9001:2015 REACH
  • L-α-Phosphatidyleth an olamine
  • Phosphatidylethanolamine (chicken egg)
  • L-α-Phosphatidylethanolamine from egg yolk
  • PE/Cephalin
  • Phosphatidylethanolamine(from egg)