30334-71-5,MFCD00067471
Catalog No.:AA00JKG9

30334-71-5 | (S)-3-Hydroxypropane-1,2-diyl dipalmitate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
25mg
≥95%
in stock  
$46.00   $32.00
- +
250mg
97%
in stock  
$73.00   $51.00
- +
1g
≥ 98% (Assay)
in stock  
$243.00   $170.00
- +
5g
97%
in stock  
$695.00   $486.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00JKG9
Chemical Name:
(S)-3-Hydroxypropane-1,2-diyl dipalmitate
CAS Number:
30334-71-5
Molecular Formula:
C35H68O5
Molecular Weight:
568.9114
MDL Number:
MFCD00067471
SMILES:
CCCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCC)CO
Properties
Computed Properties
 
Complexity:
536  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
40  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
34  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
14  

Downstream Synthesis Route
3426-89-9    30334-71-5   
Hexadecanoicacid(R)-2-(chloro-phenoxy-phosphanyloxy)-1-hexadecanoyloxymethyl-ethylester 

[1]Martin,StephenF.;Josey,JohnA.;Wong,Yue-Ling;Dean,DanielW.[JournalofOrganicChemistry,1994,vol.59,#17,p.4805-4820]

[1]Locationinpatent:experimentalpartJohns,MelloneyK.;Yin,Meng-Xin;Conway,StuartJ.;Robinson,DianeE.J.E.;Wong,LeonS.-M.;Bamert,Rebecca;Wettenhall,RichardE.H.;Holmes,AndrewB.[OrganicandBiomolecularChemistry,2009,vol.7,#18,p.3691-3697]

[2]Locationinpatent:schemeortableConway,StuartJ.;Gardiner,James;Grove,SimonJ.A.;Johns,MelloneyK.;Lim,Ze-Yi;Painter,GavinF.;Robinson,DianeE.J.E.;Schieber,Christine;Thuring,JanW.;Wong,LeonS.-M.;Yin,Meng-Xin;Burgess,AntonyW.;Catimel,Bruno;Hawkins,PhillipT.;Ktistakis,NicholasT.;Stephens,LeonardR.;Holmes,AndrewB.[OrganicandBiomolecularChemistry,2010,vol.8,#1,p.66-76]

[3]CurrentPatentAssignee:UNIVERSITYOFORLEANS;CENTRENATIONALDELARECHERCHESCIENTIFIQUE-US2011/224162,2011,A1Locationinpatent:Page/Pagecolumn10

[4]Fukase;Yoshimura;Kotani;Kusumoto[BulletinoftheChemicalSocietyofJapan,1994,vol.67,#2,p.473-482]

[5]Joffrin,AmélieM.;Saunders,AlexM.;Barneda,David;Flemington,Vikki;Thompson,AmberL.;Sanganee,HiteshJ.;Conway,StuartJ.[ChemicalScience,2021,vol.12,#7,p.2549-2557]

[1]Yamauchi,Kiyoshi;Une,Fumiyoshi;Tabata,Sachio;Kinoshita,Masayoshi[JournaloftheChemicalSociety.PerkintransactionsI,1986,p.765-770]

30334-71-5   
Methyl-phosphonicacid(1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentakis-benzyloxy-cyclohexylester6-trifluoromethyl-benzotriazol-1-ylester 
 
2,3,4,5,6-penta-O-benzyl-D-myo-inositol1-(1,2-di-O-palmitoyl-sn-glycer-3-ylmethylphosphonate) 

[1]Dreef;Douwes;Elie;VanDerMarel;VanBoom[Synthesis,1991,#6,p.443-447]

[1]Yamauchi,Kiyoshi;Une,Fumiyoshi;Tabata,Sachio;Kinoshita,Masayoshi[JournaloftheChemicalSociety.PerkintransactionsI,1986,p.765-770]

Literature

Title: Specific interactions between nucleolipid doped liposomes and DNA allow a more efficient polynucleotide condensation.

Journal: Journal of colloid and interface science 20120101

Title: Insulin action on polyunsaturated phosphatidic acid formation in rat brain: an 'in vitro' model with synaptic endings from cerebral cortex and hippocampus.

Journal: Neurochemical research 20090701

Title: Preparation, characterization, and in vivo evaluation of nanoliposomes-encapsulated bevacizumab (avastin) for intravitreal administration.

Journal: Retina (Philadelphia, Pa.) 20090501

Title: Phase separation is induced by phenothiazine derivatives in phospholipid/sphingomyelin/cholesterol mixtures containing low levels of cholesterol and sphingomyelin.

Journal: Biophysical chemistry 20071001

Title: Sum frequency generation spectroscopic study of the condensation effect of cholesterol on a lipid monolayer.

Journal: Analytical and bioanalytical chemistry 20070501

Title: Phospholipid transfer protein augments apoptosis in THP-1-derived macrophages induced by lipolyzed hypertriglyceridemic plasma.

Journal: Arteriosclerosis, thrombosis, and vascular biology 20070401

Title: Galactose-derived phosphonate analogues as potential inhibitors of phosphatidylinositol biosynthesis in mycobacteria.

Journal: Organic & biomolecular chemistry 20070321

Title: Amended final report on the safety assessment of glyceryl dilaurate, glyceryl diarachidate, glyceryl dibehenate, glyceryl dierucate, glyceryl dihydroxystearate, glyceryl diisopalmitate, glyceryl diisostearate, glyceryl dilinoleate, glyceryl dimyristate, glyceryl dioleate, glyceryl diricinoleate, glyceryl dipalmitate, glyceryl dipalmitoleate, glyceryl distearate, glyceryl palmitate lactate, glyceryl stearate citrate, glyceryl stearate lactate, and glyceryl stearate succinate.

Journal: International journal of toxicology 20070101

Title: pH-Dependent interaction of cytochrome c with mitochondrial mimetic membranes: the role of an array of positively charged amino acids.

Journal: The Journal of biological chemistry 20051014

Title: Effect of ion-binding and chemical phospholipid structure on the nanomechanics of lipid bilayers studied by force spectroscopy.

Journal: Biophysical journal 20050901

Title: [Full atomic computer model of a bilayer membrane with MAO A].

Journal: Biomeditsinskaia khimiia 20040101

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SDS
Tags:30334-71-5 Molecular Formula|30334-71-5 MDL|30334-71-5 SMILES|30334-71-5 (S)-3-Hydroxypropane-1,2-diyl dipalmitate
Catalog No.: AA00JKG9
30334-71-5,MFCD00067471
30334-71-5 | (S)-3-Hydroxypropane-1,2-diyl dipalmitate
Pack Size: 25mg
Purity: ≥95%
in stock
$46.00 $32.00
Pack Size: 250mg
Purity: 97%
in stock
$73.00 $51.00
Pack Size: 1g
Purity: ≥ 98% (Assay)
in stock
$243.00 $170.00
Pack Size: 5g
Purity: 97%
in stock
$695.00 $486.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00JKG9
Chemical Name: (S)-3-Hydroxypropane-1,2-diyl dipalmitate
CAS Number: 30334-71-5
Molecular Formula: C35H68O5
Molecular Weight: 568.9114
MDL Number: MFCD00067471
SMILES: CCCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCC)CO
Properties
Complexity: 536  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 40  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 34  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 14  
Downstream Synthesis Route
3426-89-9    30334-71-5   
Hexadecanoicacid(R)-2-(chloro-phenoxy-phosphanyloxy)-1-hexadecanoyloxymethyl-ethylester 

[1]Martin,StephenF.;Josey,JohnA.;Wong,Yue-Ling;Dean,DanielW.[JournalofOrganicChemistry,1994,vol.59,#17,p.4805-4820]

30334-71-5    108549-21-9    120595-85-9 

[1]Locationinpatent:experimentalpartJohns,MelloneyK.;Yin,Meng-Xin;Conway,StuartJ.;Robinson,DianeE.J.E.;Wong,LeonS.-M.;Bamert,Rebecca;Wettenhall,RichardE.H.;Holmes,AndrewB.[OrganicandBiomolecularChemistry,2009,vol.7,#18,p.3691-3697]

[2]Locationinpatent:schemeortableConway,StuartJ.;Gardiner,James;Grove,SimonJ.A.;Johns,MelloneyK.;Lim,Ze-Yi;Painter,GavinF.;Robinson,DianeE.J.E.;Schieber,Christine;Thuring,JanW.;Wong,LeonS.-M.;Yin,Meng-Xin;Burgess,AntonyW.;Catimel,Bruno;Hawkins,PhillipT.;Ktistakis,NicholasT.;Stephens,LeonardR.;Holmes,AndrewB.[OrganicandBiomolecularChemistry,2010,vol.8,#1,p.66-76]

[3]CurrentPatentAssignee:UNIVERSITYOFORLEANS;CENTRENATIONALDELARECHERCHESCIENTIFIQUE-US2011/224162,2011,A1Locationinpatent:Page/Pagecolumn10

[4]Fukase;Yoshimura;Kotani;Kusumoto[BulletinoftheChemicalSocietyofJapan,1994,vol.67,#2,p.473-482]

[5]Joffrin,AmélieM.;Saunders,AlexM.;Barneda,David;Flemington,Vikki;Thompson,AmberL.;Sanganee,HiteshJ.;Conway,StuartJ.[ChemicalScience,2021,vol.12,#7,p.2549-2557]

30334-71-5    88981-19-5    106235-14-7 

[1]Yamauchi,Kiyoshi;Une,Fumiyoshi;Tabata,Sachio;Kinoshita,Masayoshi[JournaloftheChemicalSociety.PerkintransactionsI,1986,p.765-770]

30334-71-5   
Methyl-phosphonicacid(1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentakis-benzyloxy-cyclohexylester6-trifluoromethyl-benzotriazol-1-ylester 
 
2,3,4,5,6-penta-O-benzyl-D-myo-inositol1-(1,2-di-O-palmitoyl-sn-glycer-3-ylmethylphosphonate) 

[1]Dreef;Douwes;Elie;VanDerMarel;VanBoom[Synthesis,1991,#6,p.443-447]

30334-71-5    96523-35-2    106235-16-9 

[1]Yamauchi,Kiyoshi;Une,Fumiyoshi;Tabata,Sachio;Kinoshita,Masayoshi[JournaloftheChemicalSociety.PerkintransactionsI,1986,p.765-770]

Literature fold

Title: Specific interactions between nucleolipid doped liposomes and DNA allow a more efficient polynucleotide condensation.

Journal: Journal of colloid and interface science20120101

Title: Insulin action on polyunsaturated phosphatidic acid formation in rat brain: an 'in vitro' model with synaptic endings from cerebral cortex and hippocampus.

Journal: Neurochemical research20090701

Title: Preparation, characterization, and in vivo evaluation of nanoliposomes-encapsulated bevacizumab (avastin) for intravitreal administration.

Journal: Retina (Philadelphia, Pa.)20090501

Title: Phase separation is induced by phenothiazine derivatives in phospholipid/sphingomyelin/cholesterol mixtures containing low levels of cholesterol and sphingomyelin.

Journal: Biophysical chemistry20071001

Title: Sum frequency generation spectroscopic study of the condensation effect of cholesterol on a lipid monolayer.

Journal: Analytical and bioanalytical chemistry20070501

Title: Phospholipid transfer protein augments apoptosis in THP-1-derived macrophages induced by lipolyzed hypertriglyceridemic plasma.

Journal: Arteriosclerosis, thrombosis, and vascular biology20070401

Title: Galactose-derived phosphonate analogues as potential inhibitors of phosphatidylinositol biosynthesis in mycobacteria.

Journal: Organic & biomolecular chemistry20070321

Title: Amended final report on the safety assessment of glyceryl dilaurate, glyceryl diarachidate, glyceryl dibehenate, glyceryl dierucate, glyceryl dihydroxystearate, glyceryl diisopalmitate, glyceryl diisostearate, glyceryl dilinoleate, glyceryl dimyristate, glyceryl dioleate, glyceryl diricinoleate, glyceryl dipalmitate, glyceryl dipalmitoleate, glyceryl distearate, glyceryl palmitate lactate, glyceryl stearate citrate, glyceryl stearate lactate, and glyceryl stearate succinate.

Journal: International journal of toxicology20070101

Title: pH-Dependent interaction of cytochrome c with mitochondrial mimetic membranes: the role of an array of positively charged amino acids.

Journal: The Journal of biological chemistry20051014

Title: Effect of ion-binding and chemical phospholipid structure on the nanomechanics of lipid bilayers studied by force spectroscopy.

Journal: Biophysical journal20050901

Title: [Full atomic computer model of a bilayer membrane with MAO A].

Journal: Biomeditsinskaia khimiia20040101

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