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105-70-4,MFCD00008717
Catalog No.:AA00389X

105-70-4 | 1,2,3-Propanetriol,1,3-diacetate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
25g
2 weeks  
$847.00   $593.00
- +
50g
2 weeks  
$909.00   $636.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00389X
Chemical Name:
1,2,3-Propanetriol,1,3-diacetate
CAS Number:
105-70-4
Molecular Formula:
C7H12O5
Molecular Weight:
176.1672
MDL Number:
MFCD00008717
SMILES:
OC(COC(=O)C)COC(=O)C
Properties
Computed Properties
 
Complexity:
147  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
6  
XLogP3:
-0.6  

Downstream Synthesis Route

[1]Drelinkiewicz;Kalemba-Jaje;Lalik;Ziȩba;Mucha;Konyushenko;Stejskal[AppliedCatalysisA:General,2013,vol.455,p.92-106]

[2]Simons[JournaloftheAmericanChemicalSociety,1926,vol.48,p.1992]

[1]Suemune;Mizuhara;Akita;Sakai[ChemicalandPharmaceuticalBulletin,1986,vol.34,#8,p.3440-3444]

dimethylsulfoxide(DMSO) 
  79-37-8    105-70-4    6946-10-7 

[1]CurrentPatentAssignee:ASTELLASPHARMAINC.-US6884868,2005,B1

[1]CurrentPatentAssignee:MONASHUNIVERSITY;PURETECHHEALTHPLC-WO2021/159021,2021,A1Locationinpatent:Paragraph00738;00740

[2]CurrentPatentAssignee:MONASHUNIVERSITY;PURETECHHEALTHPLC-WO2021/159021,2021,A1Locationinpatent:Paragraph00738;00740

[3]Locationinpatent:experimentalpartLange,Kathrin;Koenig,Andreas;Roegler,Carolin;Seeling,Andreas;Lehmann,Jochen[BioorganicandMedicinalChemistryLetters,2009,vol.19,#11,p.3141-3144]

[4]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-WO2021/38509,2021,A1Locationinpatent:Page/Pagecolumn71

[1]Locationinpatent:experimentalpartRezayat,Marzieh;Ghaziaskar,HassanS.[GreenChemistry,2009,vol.11,#5,p.710-715]

[2]Locationinpatent:experimentalpartJagadeeswaraiah;Balaraju;Prasad,P.S.Sai;Lingaiah[AppliedCatalysisA:General,2010,vol.386,#1-2,p.166-170]

[3]CurrentPatentAssignee:SOLVAY-EP2272818,2011,A1Locationinpatent:Page/Pagecolumn7

[4]CurrentPatentAssignee:SOLVAY-WO2011/1249,2011,A1Locationinpatent:Page/Pagecolumn12-13

[5]Locationinpatent:experimentalpartLiu,Xiumei;Ma,Huiyuan;Wu,Yue;Wang,Chang;Yang,Miao;Yan,Peifang;Welz-Biermann,Urs[GreenChemistry,2011,vol.13,#3,p.697-701]

[6]Zhu,Shanhui;Gao,Xiaoqing;Dong,Fang;Zhu,Yulei;Zheng,Hongyan;Li,Yongwang[JournalofCatalysis,2013,vol.306,p.155-163]

[7]Leng,Yan;Zhao,Jiwei;Jiang,Pingping;Lu,Dan[Catalysisscienceandtechnology,2016,vol.6,#3,p.875-881]

[8]Pankajakshan,Arun;Pudi,SatyanarayanaMurty;Biswas,Prakash[InternationalJournalofChemicalKinetics,2018,vol.50,#2,p.98-111]

Literature

Title: Hydrolysis of triacetin catalyzed by immobilized lipases: effect of the immobilization protocol and experimental conditions on diacetin yield.

Journal: Enzyme and microbial technology 20110506

Title: Determination of the composition of acetylglycerol mixtures by (1)H NMR followed by GC investigation.

Journal: Analytical chemistry 20081115

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SDS
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