Catalog No.:AA003TX5

3681-78-5 | Propyl laurate

Name: Name:Propyl laurate
Brand: AABLOCKS
SKU: AA003TX5
Availability: InStock
Rating: 90 (10 reviews)

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Quantity

97%

in stock

$6.00 $4.00

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97%

in stock

$21.00 $15.00

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10g

97%

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$26.00 $18.00

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100g

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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA003TX5

Chemical Name:

Propyl laurate

CAS Number:

3681-78-5

Molecular Formula:

C15H30O2

Molecular Weight:

242.3975

MDL Number:

MFCD00056190

SMILES:

CCCCCCCCCCCC(=O)OCCC

NSC Number:

42573

Properties

BP:

290.3 °C at 760 mmHg

Form:

Liquid

MP:

4.2°C (estimate)

Refractive Index:

1.4335

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

166

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

XLogP3:

6.2

Upstream Synthesis Route

71-23-8

2146-71-6

3681-78-5

[1]ProcessBiochemistry,2015,vol.50,#8,p.1224-1236

71-23-8

143-07-7

3681-78-5

[1]Patent:US6350896,2002,B1,.Locationinpatent:Example6

[2]ChemistryLetters,1997,#1,p.55-56

[3]OrganicPreparationsandProceduresInternational,2005,vol.37,#1,p.87-92

[4]MedicinalChemistryResearch,2011,vol.20,#6,p.769-781

[5]AgriculturalandBiologicalChemistry,1987,vol.51,#8,p.2153-2160

[6]JustusLiebigsAnnalenderChemie,1929,vol.473,p.255

[7]AdvancedSynthesisandCatalysis,2006,vol.348,#1-2,p.75-81

[8]AdvancedSynthesisandCatalysis,2011,vol.353,#13,p.2522-2528

[9]JournalofMolecularCatalysisB:Enzymatic,2012,vol.77,p.81-86

[10]Patent:US2013/303796,2013,A1,.Locationinpatent:Paragraph0024;0026

[11]ChemCatChem,2016,vol.8,#22,p.3446-3452

71-23-8

111-82-0

3681-78-5

[1]SyntheticCommunications,1999,vol.29,#7,p.1129-1133

[2]ChemistryLetters,1997,#1,p.55-56

71-23-8

1956-11-2

3681-78-5

[1]CatalysisLetters,2012,vol.142,#11,p.1361-1368

71-23-8

112-16-3

3681-78-5

[1]JournaloftheAmericanOilChemists'Society,1947,vol.24,p.257

Downstream Synthesis Route

71-23-8

143-07-7

3681-78-5

[1]Patent:US6350896,2002,B1.Locationinpatent:Example6

[2]ChemistryLetters,1997,p.55-56

[3]OrganicPreparationsandProceduresInternational,2005,vol.37,p.87-92

[4]MedicinalChemistryResearch,2011,vol.20,p.769-781

[5]AgriculturalandBiologicalChemistry,1987,vol.51,p.2153-2160

[6]JustusLiebigsAnnalenderChemie,1929,vol.473,p.255

[7]AdvancedSynthesisandCatalysis,2006,vol.348,p.75-81

[8]AdvancedSynthesisandCatalysis,2011,vol.353,p.2522-2528

[9]JournalofMolecularCatalysisB:Enzymatic,2012,vol.77,p.81-86

[10]Patent:US2013/303796,2013,A1.Locationinpatent:Paragraph0024;0026

[11]ChemCatChem,2016,vol.8,p.3446-3452

71-23-8

112-16-3

3681-78-5

[1]JournaloftheAmericanOilChemists'Society,1947,vol.24,p.257

71-23-8

111-82-0

3681-78-5

[1]SyntheticCommunications,1999,vol.29,p.1129-1133

[2]ChemistryLetters,1997,p.55-56

143-07-7

undecanol-5,undecanol-6

3681-78-5

[1]ChemistryLetters,1997,p.55-56

3681-78-5

112-53-8

2437-25-4

[1]Tetrahedron,2011,vol.67,p.3809-3814

Literature

Title: The metagenome-derived enzymes LipS and LipT increase the diversity of known lipases.

Journal: PloS one 20120101

Title: Continuous production of lipase-catalyzed biodiesel in a packed-bed reactor: optimization and enzyme reuse study.

Journal: Journal of biomedicine & biotechnology 20110101

Title: Unexpected reaction profile observed in the synthesis of propyl laurate when using Candida rugosa lipases immobilized in microemulsions based organogels.

Journal: Biotechnology letters 20041001

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SDS