1-oleoyl-2-hydroxy-sn-glycero-3-phosphocholine

Modify Date: 2024-01-02 18:29:53

1-oleoyl-2-hydroxy-sn-glycero-3-phosphocholine Structure
1-oleoyl-2-hydroxy-sn-glycero-3-phosphocholine structure
Common Name 1-oleoyl-2-hydroxy-sn-glycero-3-phosphocholine
CAS Number 19420-56-5 Molecular Weight 521.66700
Density N/A Boiling Point N/A
Molecular Formula C26H52NO7P Melting Point N/A
MSDS USA Flash Point N/A

 Names

Name 1-Oleoyl-sn-glycero-3-phosphocholine
Synonym More Synonyms

 Chemical & Physical Properties

Molecular Formula C26H52NO7P
Molecular Weight 521.66700
Exact Mass 521.34800
PSA 114.93000
LogP 6.20600
Storage condition -20°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Safety Phrases 22-24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2923900090

 Synthetic Route

~%

1-oleoyl-2-hydroxy-sn-glycero-3-phosphocholine Structure

1-oleoyl-2-hydr...

CAS#:19420-56-5

Literature: Chem SPA Patent: US2006/79703 A1, 2006 ; Location in patent: Page/Page column 3-4 ;

~97%

1-oleoyl-2-hydroxy-sn-glycero-3-phosphocholine Structure

1-oleoyl-2-hydr...

CAS#:19420-56-5

Literature: Fasoli, Ezio; Arnone, Alberto; Caligiuri, Antonio; D'Arrigo, Paola; De Ferra, Lorenzo; Servi, Stefano Organic and Biomolecular Chemistry, 2006 , vol. 4, # 15 p. 2974 - 2978

~%

1-oleoyl-2-hydroxy-sn-glycero-3-phosphocholine Structure

1-oleoyl-2-hydr...

CAS#:19420-56-5

Literature: CHEMI S.p.A. Patent: EP1650215 A1, 2006 ; Location in patent: Page/Page column 7 ;

 Precursor & DownStream

Precursor  2

DownStream  0

 Customs

HS Code 2923900090
Summary 2923900090 other quaternary ammonium salts and hydroxides。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

 Articles7

More Articles
Polyoxometalates--potent and selective ecto-nucleotidase inhibitors.

Biochem. Pharmacol. 93(2) , 171-81, (2015)

Polyoxometalates (POMs) are inorganic cluster metal complexes that possess versatile biological activities, including antibacterial, anticancer, antidiabetic, and antiviral effects. Their mechanisms o...

Bioactive lysophospholipids generated by hepatic lipase degradation of lipoproteins lead to complement activation via the classical pathway.

Invest. Ophthalmol. Vis. Sci. 55(10) , 6187-93, (2014)

We determined bioactivity of lysophospholipids generated by degradation of the low-density (LDL), very low-density (VLDL), and high-density (HDL) lipoproteins with hepatic lipase (HL), cholesterol est...

Characterization of lysophospholipid metabolizing enzymes in human brain.

J. Neurochem. 63 , 1839-1848, (1994)

Lysophospholipids are generated during the turnover and breakdown of membrane phospholipids. We have identified and partially characterized three enzymes involved in the metabolism of lysophospholipid...

 Synonyms

1--(9Z-octadecenoyl)-sn-glycero-3-phosphocholine
L-α-LYSOPHOSPHATIDYLCHOLINE, OLEOYL
1-oleoyl-2-hydroxy-sn-glycero-3-phosphocholine
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