Home Other Building Blocks 629-76-5
629-76-5,MFCD00004759
Catalog No.:AA003EIF

629-76-5 | 1-Pentadecanol

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Purity
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5g
98%
in stock  
$17.00   $12.00
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10g
98%
in stock  
$31.00   $22.00
- +
25g
98%
in stock  
$65.00   $46.00
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100g
98%
in stock  
$230.00   $161.00
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500g
>95.0%(GC)
in stock  
$796.00   $557.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003EIF
Chemical Name:
1-Pentadecanol
CAS Number:
629-76-5
Molecular Formula:
C15H32O
Molecular Weight:
228.4140
MDL Number:
MFCD00004759
SMILES:
CCCCCCCCCCCCCCCO
NSC Number:
66446
Properties
Properties
 
BP:
298.5 °C at 760 mmHg  
Form:
Solid  
MP:
41-44 °C(lit. )  
Refractive Index:
1.4507 (589.3 nm 0℃)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
112  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
13  
XLogP3:
6.8  

Downstream Synthesis Route

[1]Goggans;Copenhaver[JournaloftheAmericanChemicalSociety,1939,vol.61,p.2909]

[2]Wienhaus;Mucke[ChemischeBerichte,1942,vol.75,p.1830,1836]

[1]Dauben[JournaloftheAmericanChemicalSociety,1948,vol.70,p.1378]

111-48-8    629-76-5   
bis-(2-pentadecyloxy-ethyl)-sulfide 

[1]Richteretal.[JournaloftheAmericanChemicalSociety,1952,vol.74,p.4076]

[1]Dauben[JournaloftheAmericanChemicalSociety,1948,vol.70,p.1378]

[2]Panics[MonatsheftefurChemie,1894,vol.15,p.13]

[3]Cope,A.C.etal.[JournaloftheAmericanChemicalSociety,1966,vol.88,p.4228-4235]

[1]Dauben[JournaloftheAmericanChemicalSociety,1948,vol.70,p.1378]

Literature

Title: Essential oil of Myrica esculenta Buch. Ham.: composition, antimicrobial and topical anti-inflammatory activities.

Journal: Natural product research 20120101

Title: Effects of fatty acid activation on photosynthetic production of fatty acid-based biofuels in Synechocystis sp. PCC6803.

Journal: Biotechnology for biofuels 20120101

Title: Fatty acyl-CoA reductases of birds.

Journal: BMC biochemistry 20110101

Title: Three Arabidopsis fatty acyl-coenzyme A reductases, FAR1, FAR4, and FAR5, generate primary fatty alcohols associated with suberin deposition.

Journal: Plant physiology 20100801

Title: Contribution of the bees and combs to honey volatiles: blank-trial probe for chemical profiling of honey biodiversity.

Journal: Chemistry & biodiversity 20100501

Title: Binding specificity of locust odorant binding protein and its key binding site for initial recognition of alcohols.

Journal: Insect biochemistry and molecular biology 20090701

Title: Analytical method for determination of allylic isoprenols in rat tissues by liquid chromatography/tandem mass spectrometry following chemical derivatization with 3-nitrophtalic anhydride.

Journal: Journal of pharmaceutical and biomedical analysis 20080715

Title: The effect of various drying techniques on apricot volatiles analysed using direct thermal desorption-GC-TOF/MS.

Journal: Talanta 20070915

Title: Sex pheromone of the pine sawfly, Gilpinia pallida: chemical identification, synthesis, and biological activity.

Journal: Journal of chemical ecology 20061101

Title: Probing the nucleation mechanism for the binary n-nonane/1-alcohol series with atomistic simulations.

Journal: The journal of physical chemistry. B 20060921

Title: Suppression of ionization and optimization of assay for 3-hydroxy fatty acids in house dust using ion-trap mass spectrometry.

Journal: American journal of industrial medicine 20060401

Title: Novel antagonists of alcohol inhibition of l1-mediated cell adhesion: multiple mechanisms of action.

Journal: Molecular pharmacology 20021101

Title: Release rates for pine sawfly pheromones from two types of dispensers and phenology of Neodiprion sertifer.

Journal: Journal of chemical ecology 20010401

Title: I Kubo, et al. Naturally occurring antiacne agents. J Nat Prod. 1994 Jan;57(1):9-17.

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SDS
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