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Home Other Building Blocks 764-89-6
764-89-6,MFCD00792446
Catalog No.:AA005XPW

764-89-6 | 8-Hydroxyoctanoic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
97%
in stock  
$16.00   $11.00
- +
250mg
97%
in stock  
$19.00   $14.00
- +
1g
97%
in stock  
$24.00   $17.00
- +
5g
97%
in stock  
$77.00   $54.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA005XPW
Chemical Name:
8-Hydroxyoctanoic acid
CAS Number:
764-89-6
Molecular Formula:
C8H16O3
Molecular Weight:
160.2108
MDL Number:
MFCD00792446
SMILES:
OCCCCCCCC(=O)O
Properties
Properties
 
BP:
298.9 °C at 760 mmHg  
Form:
Solid  
MP:
59-63 °C  
Refractive Index:
1.4370 (estimate)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
102  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
7  
XLogP3:
-0.1  

Upstream Synthesis Route

[1]CatalysisToday,2016,vol.265,p.231-239

[1]JournaloftheAmericanChemicalSociety,1991,vol.113,#20,p.7697-7705

[2]SyntheticCommunications,2014,vol.44,#8,p.1149-1154

[3]JournaloftheAmericanChemicalSociety,1991,vol.113,#20,p.7697-7705

[4]JournalofOrganicChemistry,1964,vol.29,p.3517-3520

[5]JournalofOrganicChemistry,1996,vol.61,#14,p.4560-4567

[6]JournalofOrganicChemistry,2006,vol.71,#22,p.8545-8551

[7]OrganicandBiomolecularChemistry,2009,vol.7,#4,p.725-732

[8]OrganicProcessResearchandDevelopment,2006,vol.10,#3,p.481-483

[9]JournalofAgriculturalandFoodChemistry,2016,vol.64,#48,p.9214-9223

[1]Patent:EP2680005,2014,A1,.Locationinpatent:Page/Pagecolumn

[2]Patent:US10058612,2018,B2,.Locationinpatent:Page/Pagecolumn46

[1]JournalofOrganicChemistry,2006,vol.71,#12,p.4516-4520

[1]OrganicProcessResearchandDevelopment,2006,vol.10,#3,p.481-483

[2]SyntheticCommunications,2014,vol.44,#8,p.1149-1154

[3]JournalofAgriculturalandFoodChemistry,2016,vol.64,#48,p.9214-9223

Downstream Synthesis Route

[1]BulletinoftheChemicalSocietyofJapan,1979,vol.52,p.1989-1993

[1]AngewandteChemie,1977,vol.89,p.914-915

75-77-4    764-89-6   
C14H32O3Si2 

[1]ChemistryLetters,1993,p.907-910

[1]Heterocycles,1993,vol.35,p.1289-1307

[1]ChemicalCommunications,2015,vol.51,p.10471-10474

[2]JournaloftheAmericanChemicalSociety,1980,vol.102,p.7578-7579

[3]ChemistryLetters,1993,p.907-910

Literature

Title: A natural plasmid uniquely encodes two biosynthetic pathways creating a potent anti-MRSA antibiotic.

Journal: PloS one 20110101

Title: Medium-chain fatty acids and glutathione derivatives as inhibitors of S-nitrosoglutathione reduction mediated by alcohol dehydrogenase 3.

Journal: Chemico-biological interactions 20090615

Title: Effects of insemination quantity on honey bee queen physiology.

Journal: PloS one 20070101

Title: [Biosynthesis of multicomponent polyhydroxyalkanoates by Wautersia eutropha].

Journal: Mikrobiologiia 20070101

Title: Surface ultrastructure of SARS coronavirus revealed by atomic force microscopy.

Journal: Cellular microbiology 20051201

Title: Identification of the several new radicals formed in the reaction mixture of oxidized linoleic acid with ferrous ions using HPLC-ESR and HPLC-ESR-MS.

Journal: Free radical research 20030901

Title: Desaturation, chain scission, and register-shift of oxygen-substituted fatty acids during reaction with stearoyl-ACP desaturase.

Journal: Biochemistry 20020806

Title: Thermoanaerobacter yonseiensis sp. nov., a novel extremely thermophilic, xylose-utilizing bacterium that grows at up to 85 degrees C.

Journal: International journal of systematic and evolutionary microbiology 20010701

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