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1-O-HEXADECYL-SN-GLYCERO-3-PHOSPHOCHOLINE

Product Name
1-O-HEXADECYL-SN-GLYCERO-3-PHOSPHOCHOLINE
CAS No.
52691-62-0
Chemical Name
1-O-HEXADECYL-SN-GLYCERO-3-PHOSPHOCHOLINE
Synonyms
LYSO-PAF16;1-hexadecyl;C16 LYSO PAF;LYSO-PAF (C16);Lyso-PAF (C16),98%;FITC-Lyso-PAF C-16;LYSO-PLATELET ACTIVATING FACTOR;LYSO-PLATELET ACTIVATING FACTOR-16;LYSO-PLATELET ACTIVATING FACTOR (C16);1-O-Alkyl-sn-glycero-3-phosphocholine
CBNumber
CB1188420
Molecular Formula
C24H52NO6P
Formula Weight
481.65
MOL File
52691-62-0.mol
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1-O-HEXADECYL-SN-GLYCERO-3-PHOSPHOCHOLINE Property

Melting point:
>240 °C
storage temp. 
−20°C
solubility 
DMF: 10 mg/ml; DMSO: 10 mg/ml; Ethanol: 10 mg/ml; PBS (pH 7.2): 10 mg/ml; Water: 20 mg/ml
form 
A lyophilized powder
pka
1.209±0.50(predicted)
color 
White to off-white
biological source
synthetic
CAS DataBase Reference
52691-62-0
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Safety

Safety Statements 
22-24/25
WGK Germany 
3
10-21
HS Code 
33011300
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
L5016
Product name
1-O-Palmityl-sn-glycero-3-phosphocholine
Purity
≥99%, synthetic
Packaging
1mg
Price
$184
Updated
2025/07/31
Sigma-Aldrich
Product number
L5016
Product name
1-O-Palmityl-sn-glycero-3-phosphocholine
Purity
≥99%, synthetic
Packaging
10mg
Price
$686
Updated
2025/07/31
Cayman Chemical
Product number
60906
Product name
Lyso-PAF C-16
Purity
≥98%
Packaging
5mg
Price
$70
Updated
2024/03/01
Cayman Chemical
Product number
60906
Product name
Lyso-PAF C-16
Purity
≥98%
Packaging
10mg
Price
$120
Updated
2024/03/01
Cayman Chemical
Product number
60906
Product name
Lyso-PAF C-16
Purity
≥98%
Packaging
1mg
Price
$36
Updated
2024/03/01
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1-O-HEXADECYL-SN-GLYCERO-3-PHOSPHOCHOLINE Chemical Properties,Usage,Production

Description

Lyso-PAF C-16 can be formed by either the action of PAF-AH on PAF C-16, or by the action of a CoA-independent transacylase on 1-O-hexadecyl-2-acyl-glycerophosphocholine. Lyso-PAF C-16 is a substrate for either PAF C-16 formation by the remodeling pathway or selective acylation with arachidonic acid by a CoA-independent transacylase.

Chemical Properties

white solid

Uses

Lyso-PAF C-16 can be formed by either the action of PAF-AH on PAF C-16, or by the action of a CoA-independent transacylase on 1-O-hexadecyl-2-acyl-glycerophosphocholine. Lyso-PAF C-16 is a substrate for either PAF C-16 formation by the remodeling pathway or selective acylation with arachidonic acid by a CoA-independent transacylase.

Uses

Lyso-PAF C-16 is an inactive platelet activating factor (PAF).

Definition

ChEBI: Lysophosphatidylcholine O-16:0/0:0 is a lysophosphatidylcholine O-16:0e in which the hexadecyl group at C-1 contains 16 carbons of which none are unsaturated. It has a role as a metabolite. It is a lysophosphatidylcholine O-16:0 and a 1-alkyl-sn-glycero-3-phosphocholine.

References

[1] D M STAFFORINI  L W T. Human plasma platelet-activating factor acetylhydrolase.[J]. Methods in molecular biology, 1999, 109: 49-58. DOI: 10.1385/1-59259-581-2:49
[2] Y. UEMURA F S T Lee. A coenzyme A-independent transacylase is linked to the formation of platelet-activating factor (PAF) by generating the lyso-PAF intermediate in the remodeling pathway.[J]. The Journal of Biological Chemistry, 1991, 50 1: 8268-8272. DOI: 10.1016/s0021-9258(18)92972-8
[3] M E VENABLE. Conversion of 1-O-[3H]alkyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine to lyso platelet-activating factor by the CoA-independent transacylase in membrane fractions of human neutrophils.[J]. The Journal of Biological Chemistry, 1991, 266 28: 18691-18698.
[4] K DEGUCHI  A D  S Murashima. [Platelet activating factor].[J]. Nihon rinsho. Japanese journal of clinical medicine, 1987, 45 5: 1115-1126.
[5] M. VENABLE. Enzymatic studies of lyso platelet-activating factor acylation in human neutrophils and changes upon stimulation.[J]. The Journal of Biological Chemistry, 1993, 49 1: 7965-7975. DOI: 10.1016/s0021-9258(18)53052-0

1-O-HEXADECYL-SN-GLYCERO-3-PHOSPHOCHOLINE Preparation Products And Raw materials

Raw materials

Preparation Products

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1-O-HEXADECYL-SN-GLYCERO-3-PHOSPHOCHOLINE Suppliers

J & K SCIENTIFIC LTD.
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18210857532; 18210857532
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jkinfo@jkchemical.com
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Meryer (Shanghai) Chemical Technology Co., Ltd.
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4006356688 18621169109
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Shenzhen Regent Biochemical Technology Co., Ltd.
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52691-62-0, 1-O-HEXADECYL-SN-GLYCERO-3-PHOSPHOCHOLINERelated Search:


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