NP-MRD: Showing NP-Card for decyl butyrate (NP0256810)

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Record Information

Version

2.0

Created at

2022-09-07 21:45:32 UTC

Updated at

2022-09-07 21:45:32 UTC

NP-MRD ID

NP0256810

Secondary Accession Numbers

None

Natural Product Identification

Common Name

decyl butyrate

Description

Decyl butanoate, also known as navan or fema 2368, belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol. Decyl butanoate is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Decyl butanoate is a slightly rose, sweet, and fruity tasting compound. decyl butyrate is found in Mandragora officinarum. Outside of the human body,.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 43  0  0  0  0  0  0  0  0999 V2000
    4.5364    2.7683   -0.6561 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4554    1.6778   -0.1560 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9494    0.3196   -0.5969 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5564    0.1128   -0.0230 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0469   -1.2299   -0.4544 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6610   -1.5037    0.0915 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6595   -0.4998   -0.3711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7327   -0.8087    0.2241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2232   -2.1446   -0.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5266   -2.5711    0.3673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6600   -1.8437    0.1583 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0768   -0.6343    0.6009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3528    0.0057    1.3671 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4103   -0.1189    0.1385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6767    1.2448    0.7519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5677    2.1683    0.2956 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8374    3.1176    0.1515 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1255    3.6309   -1.0698 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8701    2.4085   -1.4795 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4838    1.8289   -0.5555 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5273    1.7194    0.9601 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8250    0.3681   -1.7055 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6336   -0.4676   -0.2678 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8592    0.8878   -0.3457 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6037    0.1124    1.0848 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7059   -2.0294   -0.0375 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9648   -1.3085   -1.5652 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3846   -2.5039   -0.3571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6799   -1.6317    1.1855 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8913    0.5405   -0.1468 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5641   -0.5854   -1.4826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6387   -0.6560    1.3085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3432    0.0313   -0.2195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1381   -2.3175   -1.2928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4571   -2.8901    0.2225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3539   -2.7951    1.4841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7661   -3.6296   -0.0018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2130   -0.8183    0.4409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4361   -0.0052   -0.9503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6351    1.6465    0.3662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7708    1.1998    1.8563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0078    2.4750    1.2145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8583    1.6799   -0.3981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9760    3.0491   -0.2364 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  2 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  4 25  1  0
  5 26  1  0
  5 27  1  0
  6 28  1  0
  6 29  1  0
  7 30  1  0
  7 31  1  0
  8 32  1  0
  8 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
 14 38  1  0
 14 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  0
 16 43  1  0
 16 44  1  0
M  END


  Mrv0541 05061309422D          

 16 15  0  0  0  0            999 V2000
   -6.0770   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9256   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3625   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2112   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6480   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9336   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2191   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5046   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7901   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0757   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3612   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4967   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3533   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7822   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7822   -4.3974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0677   -3.1599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  1  0  0  0  0
 11 10  1  0  0  0  0
 12  4  1  0  0  0  0
 13 11  1  0  0  0  0
 14 12  1  0  0  0  0
 15 14  2  0  0  0  0
 16 13  1  0  0  0  0
 16 14  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0256810

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCOC(=O)CCC

> <INCHI_IDENTIFIER>
InChI=1S/C14H28O2/c1-3-5-6-7-8-9-10-11-13-16-14(15)12-4-2/h3-13H2,1-2H3

> <INCHI_KEY>
PUCQHFICPFUPKW-UHFFFAOYSA-N

> <FORMULA>
C14H28O2

> <MOLECULAR_WEIGHT>
228.3709

> <EXACT_MASS>
228.20893014

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
29.961087786900585

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
decyl butanoate

> <ALOGPS_LOGP>
5.81

> <JCHEM_LOGP>
5.058963858333334

> <ALOGPS_LOGS>
-5.35

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.0326196832292425

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
68.1203

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.02e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
decyl butanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0     -11.344  -5.898   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.328  -5.898   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -10.010  -6.668   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.994  -6.668   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.676  -5.898   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.343  -6.668   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.009  -5.898   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.675  -6.668   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.342  -5.898   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.008  -6.668   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.674  -5.898   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.661  -5.898   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.659  -6.668   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.327  -6.668   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.327  -8.208   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       1.993  -5.898   0.000  0.00  0.00           O+0
CONECT    1    3                                                            
CONECT    2    4                                                            
CONECT    3    1    5                                                       
CONECT    4    2   12                                                       
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   13                                                       
CONECT   12    4   14                                                       
CONECT   13   11   16                                                       
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   13   14                                                       
MASTER        0    0    0    0    0    0    0    0   16    0   30    0
END

View in JSmol

Synonyms

Value	Source
Decyl butanoic acid	Generator
Butanoic acid, decyl ester	HMDB
Butyric acid, decyl ester	HMDB
Butyric acid, decyl ester (8ci)	HMDB
Decyl butyrate	HMDB
FEMA 2368	HMDB
N-Decyl butanoate	HMDB
Navan	HMDB
Navane	HMDB
Navaron	HMDB
Orbinamon	HMDB
Thiothixene	HMDB
Thiothixine	HMDB
Tiotixene	HMDB
Decyl butyric acid	Generator

Chemical Formula

C₁₄H₂₈O₂

Average Mass

228.3709 Da

Monoisotopic Mass

228.20893 Da

IUPAC Name

decyl butanoate

Traditional Name

decyl butanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCOC(=O)CCC

InChI Identifier

InChI=1S/C14H28O2/c1-3-5-6-7-8-9-10-11-13-16-14(15)12-4-2/h3-13H2,1-2H3

InChI Key

PUCQHFICPFUPKW-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Mandragora officinarum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohol esters

Direct Parent

Fatty alcohol esters

Alternative Parents

Substituents

Fatty alcohol ester
Fatty acid ester
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Wax monoesters (LMFA07010422 )

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	5.81	ALOGPS
logP	5.06	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Basic)	-7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	68.12 m³·mol⁻¹	ChemAxon
Polarizability	29.96 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0037312

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB016331

KNApSAcK ID

Not Available

Chemspider ID

199704

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

229387

PDB ID

Not Available

ChEBI ID

23580

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for decyl butyrate (NP0256810)

MOL for NP0256810 (decyl butyrate)

3D MOL for NP0256810 (decyl butyrate)

3D SDF for NP0256810 (decyl butyrate)

3D-SDF for NP0256810 (decyl butyrate)

PDB for NP0256810 (decyl butyrate)

3D PDB for NP0256810 (decyl butyrate)

SMILES for NP0256810 (decyl butyrate)

INCHI for NP0256810 (decyl butyrate)

Structure for NP0256810 (decyl butyrate)

3D Structure for NP0256810 (decyl butyrate)