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23597-82-2,MFCD00023587
Catalog No.:AA002NQP

23597-82-2 | Hexyl nicotinoate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
95%
in stock  
$18.00   $13.00
- +
5g
95%
in stock  
$29.00   $20.00
- +
25g
98%
in stock  
$58.00   $41.00
- +
100g
98%
in stock  
$204.00   $143.00
- +
500g
98%
in stock  
$809.00   $567.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA002NQP
Chemical Name:
Hexyl nicotinoate
CAS Number:
23597-82-2
Molecular Formula:
C12H17NO2
Molecular Weight:
207.2689
MDL Number:
MFCD00023587
SMILES:
CCCCCCOC(=O)c1cccnc1
NSC Number:
72758
Properties
Properties
 
BP:
329.1°C at 760 mmHg  
Form:
Liquid  
Refractive Index:
1.4880 to 1.4920  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
183  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
3  
Rotatable Bond Count:
7  
XLogP3:
3.6  

Downstream Synthesis Route

[1]CurrentPatentAssignee:VIATRISINC-DE946541,1952,C

[2]CurrentPatentAssignee:VIATRISINC-DE952714,1951,C

[3]CurrentPatentAssignee:VALEROENERGYCORPORATION'SOILREFINERYINKROTZSPRINGS-US2816112,1954,A

[1]Badgettetal.[JournaloftheAmericanChemicalSociety,1945,vol.67,p.1135,1136]

[1]CurrentPatentAssignee:Aries-US2861077,1955,A

[1]Huberetal.[JournaloftheAmericanChemicalSociety,1946,vol.68,p.187,189]

[2]Williams,HywelD.;Sahbaz,Yasemin;Ford,Leigh;Nguyen,Tri-Hung;Scammells,PeterJ.;Porter,ChristopherJ.H.[ChemicalCommunications,2014,vol.50,#14,p.1688-1690]

23597-82-2   
perfluoro-cis-2-n-butyl-3-n-propyloxaziridine 
 
3-HexyloxycarbonylpyridineN-oxide 
 
3-Hexyloxycarbonyl-N-(perfluorobutanoyl)pyridinium-1-aminide 

[1]Bernardi,Rosanna;Novo,Barbara;Resnati,Giuseppe[JournaloftheChemicalSociety.PerkintransactionsI,1996,#20,p.2517-2521]

Literature

Title: Reactions of non-immunologic contact urticaria on scalp, face, and back.

Journal: Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) 20121101

Title: Mapping the human face: biophysical properties.

Journal: Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) 20100201

Title: Microneedle penetration and injection past the stratum corneum in humans.

Journal: The Journal of dermatological treatment 20090101

Title: Estimation of serum protein binding of compounds metabolized in serum using matrix inhibition.

Journal: Biopharmaceutics & drug disposition 20080701

Title: Functional map and age-related differences in the human face: nonimmunologic contact urticaria induced by hexyl nicotinate.

Journal: Contact dermatitis 20060701

Title: Permeation, metabolism and site of action concentration of nicotinic acid derivatives in human skin. Correlation with topical pharmacological effect.

Journal: European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences 20031001

Title: Differences among moisturizers in affecting skin susceptibility to hexyl nicotinate, measured as time to increase skin blood flow.

Journal: Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) 20030201

Title: Hydration vs. skin permeability to nicotinates in man.

Journal: Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) 20020201

Title: Effect of drug lipophilicity on in vitro release rate from oil vehicles using nicotinic acid esters as model prodrug derivatives.

Journal: International journal of pharmaceutics 20010323

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SDS
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