96924-84-4

Upstream product

• 4167-02-6 2-bromoethylphosphoric acid dichloride 
• 18678-94-9 2-benzyloxy-3-hexadecyloxy-1-propanol 
• 14690-00-7 2-O-benzylglycerol 
• 137618-68-9 Benzoic acid 2-benzyloxy-3-hydroxy-propyl ester 
• 84415-89-4 (S)-2-benzyloxy-3-hexadecyloxy-propan-1-ol 
• 143516-78-3 ((R)-2-Hexadecyloxy-1-methoxymethoxymethyl-ethoxymethyl)-benzene 
• 143516-74-9 ((E)-(R)-1-Methoxymethoxymethyl-but-2-enyloxymethyl)-benzene 
• 138850-89-2 (R)-1-O-Methoxymethyl-2-O-benzylglycerol 
• 100-39-0 benzyl bromide 
• 20779-14-0 methanesulfonic acid hexadecyl ester 
• 96924-82-2 Benzoic acid 2-benzyloxy-3-hexadecyloxy-propyl ester 
• 82002-21-9 2-O-Benzyl-1-O-hexadecyl-3-O-trityl-glycerin 
• 82002-20-8 1-O-hexadecyl-3-O-trityl-rac-glycerol 
• 6145-69-3 3-(hexadecyloxy)-1,2-propanediol 

Downstream Products

• 91326-84-0 1-O-hexadecyl-2-O-benzyl-sn-glycero-3-phosphocholine 
• 74389-68-7 PAF 
• 52691-62-0 1-palmityl-sn-glycero-3-phosphocholine 
• 77286-68-1 3-O-hexadecyl-2-acetyl-sn-glycero-1-phosphocholine 
• 18678-98-3 Rac_. 1-O-Hexadecyl-2-O-benzylglycero-3-phosphocholin 
• 78119-19-4 2-hydroxy-3-(hexadecyloxy)-propyl 2-trimethylammonioethyl phosphate 
• 96924-86-6 C₂₈H₄₉BrO₆P^(1-)*Na⁽¹⁺⁾ 

Relevant academic research and scientific papers

Influence of α-branched fatty acid chains on the thermotropic behaviour of racemic 1-O-hexadecyl-2-acyl-glycero-3-phosphocholines

Phosphatidylcholines containing an α-branched palmitic acid ester linked to position C2 of the glycerol backbone were synthesized and characterized using differential scanning calorimetry and X-ray diffraction. As the length of the sidegroup substituted on the palmitic acid chain is changed, the calorimetric parameters pass through a minimum. The polymorphic behaviour is different when the sidegroup is larger, or smaller, than propyl. The comparison of the physicochemical parameters of isomers differing in the bonding of the branched chain fatty acid to the glycerol backbone (to position C1 or C2, respectively) shows that the chains are nonequivalent. Keywords: Phosphatidylcholine; Branched chain fatty acids; Microcalorimetry; X-ray diffraction; Polymorphism

Syntheses of a glycerophospholipid, C16-platelet activating factor and a palmitoyl analogue of M-5, an anti-inflammatory glyceroglycolipid

From a chiral C4-epoxide (-)-3, which is one of the synthons in our synthetic strategy for complex lipids, a glycerophospholipid C16-platelet activating factor (C16-PAF, 1) and a palmitoyl analogue (2) of an anti-inflammatory glyceroglycolipid M-5, which was previously isolated from the Okinawan marine sponge Phyllospongia foliascens, have been synthesized.