Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2012-09-11 20:06:08 UTC

Update Date

2023-02-21 17:24:38 UTC

HMDB ID

HMDB0035155

Secondary Accession Numbers

HMDB35155

Metabolite Identification

Common Name

beta-Geraniol

Description

beta-Geraniol, also known as (E)-nerol, the isomer of nerol (or geranyl alcohol, is a monoterpenoid alcohol. It belongs to the class of organic compounds known as acyclic monoterpenoids. These are monoterpenes that do not contain a cycle. Monoterpenoids are terpenes that contain 10 carbon atoms and are comprised of two isoprene units. The biosynthesis of monoterpenes is known to occur mainly through the methyl-erythritol-phosphate (MEP) pathway in the plastids (PMID:7640522 ). Geranyl diphosphate (GPP) is a key intermediate in the biosynthesis of cyclic monoterpenes. GPP undergoes several cyclization reactions to yield a diverse number of cyclic arrangements. beta-Geraniol is an isoprenoid lipid molecule that is very hydrophobic, practically insoluble in water, and relatively neutral. beta-Geraniol has a sweet, citrus, and floral taste. beta-Geraniol is found in highest concentrations in common grapes, black walnuts, and common thymes and in lower concentrations in cardamoms, common oregano, and gingers. beta-Geraniol has also been detected in lemon verbena, oval-leaf huckleberries, common pea, sweet cherries, and nopals. This could make beta-geraniol a potential biomarker for the consumption of these foods. It is found in as an alcohol and as its ester in many essential oils including geranium oil. It is the primary part of rose oil, palmarosa oil, and citronella oil (Java type) and occurs in small quantities in geranium, lemon, and many other essential oils. Geraniol is a monoterpenoid and an alcohol found in cannabis plants (PMID:6991645 ). Because it has a rose-like odor, it is commonly used in perfumes. It is used to create flavors such as peach, raspberry, grapefruit, red apple, plum, lime, orange, lemon, watermelon, pineapple, and blueberry. Geraniol is produced by the scent glands of honeybees to mark nectar-bearing flowers and locate the entrances to their hives (http//doi:10.1051/apido:19900403).

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0035155
     RDKit          3D
beta-Geraniol
 29 28  0  0  0  0  0  0  0  0999 V2000
    3.4273   -0.7263    0.1280 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5513    0.3839   -0.3295 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1484    1.7293   -0.5009 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2501    0.1493   -0.5760 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6901   -1.2092   -0.3929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4148   -1.2360    0.5746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6576   -0.5481    0.2935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6971   -0.5783    1.4032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0328    0.1053   -0.7833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3740    0.7727   -0.9080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2229    2.1444   -1.1248 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0646   -1.0785    1.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4049   -1.5283   -0.6620 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4947   -0.4068    0.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3688    2.5259   -0.3959 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9374    1.8450    0.2860 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5517    1.8017   -1.5238 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6041    0.9463   -0.9013 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4631   -1.6972   -1.3692 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5198   -1.8538    0.0301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0237   -0.8137    1.5574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6922   -2.3062    0.8465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5783   -1.0868    0.9651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8955    0.4454    1.7765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3760   -1.2345    2.2421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3347    0.1291   -1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9253    0.2637   -1.7083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9061    0.6740    0.0528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3453    2.3877   -0.7092 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
  1 12  1  0
  1 13  1  0
  1 14  1  0
  3 15  1  0
  3 16  1  0
  3 17  1  0
  4 18  1  0
  5 19  1  0
  5 20  1  0
  6 21  1  0
  6 22  1  0
  8 23  1  0
  8 24  1  0
  8 25  1  0
  9 26  1  0
 10 27  1  0
 10 28  1  0
 11 29  1  0
M  END

HMDB0035155
     RDKit          3D
beta-Geraniol
 29 28  0  0  0  0  0  0  0  0999 V2000
    3.4273   -0.7263    0.1280 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5513    0.3839   -0.3295 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1484    1.7293   -0.5009 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2501    0.1493   -0.5760 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6901   -1.2092   -0.3929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4148   -1.2360    0.5746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6576   -0.5481    0.2935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6971   -0.5783    1.4032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0328    0.1053   -0.7833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3740    0.7727   -0.9080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2229    2.1444   -1.1248 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0646   -1.0785    1.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4049   -1.5283   -0.6620 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4947   -0.4068    0.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3688    2.5259   -0.3959 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9374    1.8450    0.2860 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5517    1.8017   -1.5238 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6041    0.9463   -0.9013 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4631   -1.6972   -1.3692 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5198   -1.8538    0.0301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0237   -0.8137    1.5574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6922   -2.3062    0.8465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5783   -1.0868    0.9651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8955    0.4454    1.7765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3760   -1.2345    2.2421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3347    0.1291   -1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9253    0.2637   -1.7083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9061    0.6740    0.0528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3453    2.3877   -0.7092 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
  1 12  1  0
  1 13  1  0
  1 14  1  0
  3 15  1  0
  3 16  1  0
  3 17  1  0
  4 18  1  0
  5 19  1  0
  5 20  1  0
  6 21  1  0
  6 22  1  0
  8 23  1  0
  8 24  1  0
  8 25  1  0
  9 26  1  0
 10 27  1  0
 10 28  1  0
 11 29  1  0
M  END

COMPND    HMDB0035155
HETATM    1  C1  UNL     1       3.427  -0.726   0.128  1.00  0.00           C  
HETATM    2  C2  UNL     1       2.551   0.384  -0.330  1.00  0.00           C  
HETATM    3  C3  UNL     1       3.148   1.729  -0.501  1.00  0.00           C  
HETATM    4  C4  UNL     1       1.250   0.149  -0.576  1.00  0.00           C  
HETATM    5  C5  UNL     1       0.690  -1.209  -0.393  1.00  0.00           C  
HETATM    6  C6  UNL     1      -0.415  -1.236   0.575  1.00  0.00           C  
HETATM    7  C7  UNL     1      -1.658  -0.548   0.293  1.00  0.00           C  
HETATM    8  C8  UNL     1      -2.697  -0.578   1.403  1.00  0.00           C  
HETATM    9  C9  UNL     1      -2.033   0.105  -0.783  1.00  0.00           C  
HETATM   10  C10 UNL     1      -3.374   0.773  -0.908  1.00  0.00           C  
HETATM   11  O1  UNL     1      -3.223   2.144  -1.125  1.00  0.00           O  
HETATM   12  H1  UNL     1       3.065  -1.078   1.106  1.00  0.00           H  
HETATM   13  H2  UNL     1       3.405  -1.528  -0.662  1.00  0.00           H  
HETATM   14  H3  UNL     1       4.495  -0.407   0.164  1.00  0.00           H  
HETATM   15  H4  UNL     1       2.369   2.526  -0.396  1.00  0.00           H  
HETATM   16  H5  UNL     1       3.937   1.845   0.286  1.00  0.00           H  
HETATM   17  H6  UNL     1       3.552   1.802  -1.524  1.00  0.00           H  
HETATM   18  H7  UNL     1       0.604   0.946  -0.901  1.00  0.00           H  
HETATM   19  H8  UNL     1       0.463  -1.697  -1.369  1.00  0.00           H  
HETATM   20  H9  UNL     1       1.520  -1.854   0.030  1.00  0.00           H  
HETATM   21  H10 UNL     1      -0.024  -0.814   1.557  1.00  0.00           H  
HETATM   22  H11 UNL     1      -0.692  -2.306   0.846  1.00  0.00           H  
HETATM   23  H12 UNL     1      -3.578  -1.087   0.965  1.00  0.00           H  
HETATM   24  H13 UNL     1      -2.896   0.445   1.777  1.00  0.00           H  
HETATM   25  H14 UNL     1      -2.376  -1.234   2.242  1.00  0.00           H  
HETATM   26  H15 UNL     1      -1.335   0.129  -1.622  1.00  0.00           H  
HETATM   27  H16 UNL     1      -3.925   0.264  -1.708  1.00  0.00           H  
HETATM   28  H17 UNL     1      -3.906   0.674   0.053  1.00  0.00           H  
HETATM   29  H18 UNL     1      -2.345   2.388  -0.709  1.00  0.00           H  
CONECT    1    2   12   13   14
CONECT    2    3    4    4
CONECT    3   15   16   17
CONECT    4    5   18
CONECT    5    6   19   20
CONECT    6    7   21   22
CONECT    7    8    9    9
CONECT    8   23   24   25
CONECT    9   10   26
CONECT   10   11   27   28
CONECT   11   29
END

HMDB0035155
     RDKit          3D
beta-Geraniol
 29 28  0  0  0  0  0  0  0  0999 V2000
    3.4273   -0.7263    0.1280 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5513    0.3839   -0.3295 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1484    1.7293   -0.5009 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2501    0.1493   -0.5760 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6901   -1.2092   -0.3929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4148   -1.2360    0.5746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6576   -0.5481    0.2935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6971   -0.5783    1.4032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0328    0.1053   -0.7833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3740    0.7727   -0.9080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2229    2.1444   -1.1248 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0646   -1.0785    1.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4049   -1.5283   -0.6620 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4947   -0.4068    0.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3688    2.5259   -0.3959 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9374    1.8450    0.2860 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5517    1.8017   -1.5238 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6041    0.9463   -0.9013 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4631   -1.6972   -1.3692 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5198   -1.8538    0.0301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0237   -0.8137    1.5574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6922   -2.3062    0.8465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5783   -1.0868    0.9651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8955    0.4454    1.7765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3760   -1.2345    2.2421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3347    0.1291   -1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9253    0.2637   -1.7083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9061    0.6740    0.0528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3453    2.3877   -0.7092 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
  1 12  1  0
  1 13  1  0
  1 14  1  0
  3 15  1  0
  3 16  1  0
  3 17  1  0
  4 18  1  0
  5 19  1  0
  5 20  1  0
  6 21  1  0
  6 22  1  0
  8 23  1  0
  8 24  1  0
  8 25  1  0
  9 26  1  0
 10 27  1  0
 10 28  1  0
 11 29  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(2E)-3,7-Dimethyl-2,6-octadien-1-ol	ChEBI
(2E)-Geraniol	ChEBI
(e)-3,7-Dimethyl-2,6-octadien-1-ol	ChEBI
(e)-Geraniol	ChEBI
(e)-Nerol	ChEBI
2-trans-3,7-Dimethyl-2,6-octadien-1-ol	ChEBI
3,7-Dimethyl-trans-2,6-octadien-1-ol	ChEBI
Geranyl alcohol	ChEBI
Lemonol	ChEBI
t-Geraniol	ChEBI
trans-3,7-Dimethyl-2,6-octadien-1-ol	ChEBI
trans-Geraniol	ChEBI
b-Geraniol	Generator
Β-geraniol	Generator
(2E)-3,7-Dimethylocta-2,6-dien-1-ol	HMDB
2-trans-3,7-Dimethyl-2,6-octadiene-1-ol	HMDB
2E-Geraniol	HMDB
3,7-Dimethyl-(2E)-2,6-octadien-1-ol	HMDB
3,7-Dimethyl-(e)-2,6-octadien-1-ol	HMDB
FEMA 2507	HMDB
Geraniol	HMDB
trans-2,6-Dimethyl-2,6-octadien-8-ol	HMDB
trans-3,7-Dimethy- octa-2,6-dien-1-ol	HMDB
Geraniol, (Z)-isomer	MeSH
Geraniol, 1-(14)C-labeled, (e)-isomer	MeSH
Nerol	MeSH
Geraniol, 2-(14)C-labeled, (e)-isomer	MeSH
Geraniol, titanium (4+) salt	MeSH
Geraniol, (e)-isomer	MeSH
(E)-3,7-Dimethyl-2,6-octadienol	PhytoBank
trans-1-Hydroxy-3,7-dimethyl-2,6-octadiene	PhytoBank
beta-Geraniol	PhytoBank

Chemical Formula

C₁₀H₁₈O

Average Molecular Weight

154.253

Monoisotopic Molecular Weight

154.1357652

IUPAC Name

(2E)-3,7-dimethylocta-2,6-dien-1-ol

Traditional Name

geraniol

CAS Registry Number

106-24-1

SMILES

CC(C)=CCC\C(C)=C\CO

InChI Identifier

InChI=1S/C10H18O/c1-9(2)5-4-6-10(3)7-8-11/h5,7,11H,4,6,8H2,1-3H3/b10-7+

InChI Key

GLZPCOQZEFWAFX-JXMROGBWSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acyclic monoterpenoids. These are monoterpenes that do not contain a cycle.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Acyclic monoterpenoids

Alternative Parents

Substituents

Acyclic monoterpenoid
Fatty alcohol
Fatty acyl
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

primary alcohol (CHEBI:17447 )
monoterpenoid (CHEBI:17447 )
3,7-dimethylocta-2,6-dien-1-ol (CHEBI:17447 )
Acyclic monoterpenoids (C01500 )
Linear monoterpenes (C01500 )
Acyclic monoterpenoids (LMPR0102010016 )

Ontology

Sweet

Disposition

Biological location

Cellular substructure

Non-excretory biofluid

Biofluid or Excreta

Saliva (HMDB: HMDB0035155)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0035155)

Source

Endogenous

Endogenous (HMDB: HMDB0035155)

Plant

Animal

Animal (HMDB: HMDB0035155)

Exogenous

Food

Food (HMDB: HMDB0035155)

Animal origin

Poultry

Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)
Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)

Equine

Horse (FooDB: FOOD00378)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Herbs and Spices (FooDB: FOOD00866)

Nut

Almond (FooDB: FOOD00148)
Brazil nut (FooDB: FOOD00024)
Cashew nut (FooDB: FOOD00011)
Chestnut (FooDB: FOOD00045)
Hazelnut (FooDB: FOOD00376)
Peanut (FooDB: FOOD00016)
Pecan nut (FooDB: FOOD00044)
Pine nut (FooDB: FOOD00138)
Pistachio (FooDB: FOOD00140)
Walnut (FooDB: FOOD00608)
Acorn (FooDB: FOOD00282)
Beech nut (FooDB: FOOD00299)
Butternut (FooDB: FOOD00316)
Chinese chestnut (FooDB: FOOD00331)
European chestnut (FooDB: FOOD00363)
Hickory nut (FooDB: FOOD00377)
Macadamia nut (FooDB: FOOD00525)
Mixed nuts (FooDB: FOOD00771)
Pili nut (FooDB: FOOD00432)
Colorado pinyon (FooDB: FOOD00433)
Black walnut (FooDB: FOOD00093)
Common walnut (FooDB: FOOD00094)
Japanese chestnut (FooDB: FOOD00385)
Common hazelnut (FooDB: FOOD00062)
Macadamia nut (M. tetraphylla) (FooDB: FOOD00225)
Japanese walnut (FooDB: FOOD00240)
Nuts (FooDB: FOOD00869)

Fruit

Pome

Drupe

Apricot (FooDB: FOOD00144)
Prunus (Cherry, Plum) (FooDB: FOOD00143)
Nectarine (FooDB: FOOD00229)
Peach (FooDB: FOOD00149)
European plum (FooDB: FOOD00147)
Sour cherry (FooDB: FOOD00146)
Sweet cherry (FooDB: FOOD00145)
Common chokecherry (FooDB: FOOD00562)
Peach (var.) (FooDB: FOOD00230)

Tropical fruit

Berry

Bilberry (FooDB: FOOD00193)
Rubus (Blackberry, Raspberry) (FooDB: FOOD00160)
Vaccinium (Blueberry, Cranberry, Huckleberry) (FooDB: FOOD00188)
Blackcurrant (FooDB: FOOD00155)
Redcurrant (FooDB: FOOD00156)
Elderberry (FooDB: FOOD00358)
Gooseberry (FooDB: FOOD00157)
Grape (FooDB: FOOD00369)
Lingonberry (FooDB: FOOD00194)
Loganberry (FooDB: FOOD00400)
Strawberry (FooDB: FOOD00083)
Boysenberry (FooDB: FOOD00542)
American cranberry (FooDB: FOOD00192)
Common grape (FooDB: FOOD00204)
Strawberry guava (FooDB: FOOD00482)
Black mulberry (FooDB: FOOD00117)
Red raspberry (FooDB: FOOD00162)
Muscadine grape (FooDB: FOOD00203)
Salmonberry (FooDB: FOOD00456)
Alaska blueberry (FooDB: FOOD00380)
Sea-buckthornberry (FooDB: FOOD00087)
Black elderberry (FooDB: FOOD00166)
Black crowberry (FooDB: FOOD00075)
Black huckleberry (FooDB: FOOD00084)
Mulberry (FooDB: FOOD00116)
Black chokeberry (FooDB: FOOD00136)
Cloudberry (FooDB: FOOD00161)
Black raspberry (FooDB: FOOD00163)
Rowanberry (FooDB: FOOD00176)
Lowbush blueberry (FooDB: FOOD00189)
Sparkleberry (FooDB: FOOD00190)
Highbush blueberry (FooDB: FOOD00191)
Arctic blackberry (FooDB: FOOD00207)
Bayberry (FooDB: FOOD00209)
Elliott's blueberry (FooDB: FOOD00210)
Canada blueberry (FooDB: FOOD00211)
Bog bilberry (FooDB: FOOD00212)
Buffalo currant (FooDB: FOOD00213)
European cranberry (FooDB: FOOD00217)
Deerberry (FooDB: FOOD00218)
Cascade huckleberry (FooDB: FOOD00220)
Oval-leaf huckleberry (FooDB: FOOD00221)
Evergreen huckleberry (FooDB: FOOD00222)
Red huckleberry (FooDB: FOOD00223)
Summer grape (FooDB: FOOD00227)
Fox grape (FooDB: FOOD00228)
Half-highbush blueberry (FooDB: FOOD00248)
Jostaberry (FooDB: FOOD00257)
Sweet rowanberry (FooDB: FOOD00265)
Skunk currant (FooDB: FOOD00267)
Squashberry (FooDB: FOOD00344)
Ohelo berry (FooDB: FOOD00419)
Chinese bayberry (FooDB: FOOD00852)
Saskatoon berry (FooDB: FOOD00884)
Nanking cherry (FooDB: FOOD00885)
Evergreen blackberry (FooDB: FOOD00901)
Rabbiteye blueberry (FooDB: FOOD00898)
Blackberry (FooDB: FOOD00906)

Other fruit

Date (FooDB: FOOD00135)
Fig (FooDB: FOOD00081)
Jujube (FooDB: FOOD00388)

Citrus

Grapefruit (FooDB: FOOD00256)
Lemon (FooDB: FOOD00054)
Lime (FooDB: FOOD00053)
Sweet orange (FooDB: FOOD00057)
Mandarin orange (Clementine, Tangerine) (FooDB: FOOD00056)
Persian lime (FooDB: FOOD00543)
Pummelo (FooDB: FOOD00055)
Grapefruit/Pummelo hybrid (FooDB: FOOD00255)
Citrus (FooDB: FOOD00859)

Fruits (FooDB: FOOD00871)

Vegetable

Shoot vegetable

Fruit vegetable

Eggplant (FooDB: FOOD00174)
Avocado (FooDB: FOOD00130)
Groundcherry (FooDB: FOOD00371)
Olive (FooDB: FOOD00121)
Pepper (FooDB: FOOD00040)
Garden tomato (FooDB: FOOD00171)
Mexican groundcherry (FooDB: FOOD00491)
Green bell pepper (FooDB: FOOD00877)
Yellow bell pepper (FooDB: FOOD00878)
Red bell pepper (FooDB: FOOD00880)
Italian sweet red pepper (FooDB: FOOD00881)
Garden tomato (var.) (FooDB: FOOD00173)
Cherry tomato (FooDB: FOOD00172)
Pepper (C. baccatum) (FooDB: FOOD00231)
Pepper (C. chinense) (FooDB: FOOD00232)
Pepper (Capsicum) (FooDB: FOOD00233)
Pepper (C. frutescens) (FooDB: FOOD00428)
Pepper (C. pubescens) (FooDB: FOOD00849)
Orange bell pepper (FooDB: FOOD00879)

Root vegetable

Cabbage

Leaf vegetable

Lettuce (FooDB: FOOD00095)
Swiss chard (FooDB: FOOD00237)
Garden cress (FooDB: FOOD00099)
Endive (FooDB: FOOD00048)
Spinach (FooDB: FOOD00178)
Common beet (FooDB: FOOD00025)
Garland chrysanthemum (FooDB: FOOD00333)
Jute (FooDB: FOOD00389)
Lambsquarters (FooDB: FOOD00394)
New Zealand spinach (FooDB: FOOD00415)
Swamp cabbage (FooDB: FOOD00091)
Rocket salad (ssp.) (FooDB: FOOD00077)
Yautia (FooDB: FOOD00510)
Romaine lettuce (FooDB: FOOD00888)
Rocket salad (FooDB: FOOD00244)
Chicory leaves (FooDB: FOOD00250)
Corn salad (FooDB: FOOD00340)
Malabar spinach (FooDB: FOOD00404)
Ostrich fern (FooDB: FOOD00556)
Green vegetables (FooDB: FOOD00872)

Mushroom

Tuber

Onion-family vegetable

Leek (FooDB: FOOD00007)
Allium (FooDB: FOOD00005)
Wild leek (FooDB: FOOD00396)
Shallot (FooDB: FOOD00243)
Garden onion (FooDB: FOOD00006)
Garden onion (var.) (FooDB: FOOD00226)
Onion-family vegetables (FooDB: FOOD00855)
Green onion (FooDB: FOOD00963)
Red onion (FooDB: FOOD00962)

Other vegetable

Okra (FooDB: FOOD00420)
Horseradish tree (FooDB: FOOD00379)
Sacred lotus (FooDB: FOOD00402)
Tree fern (FooDB: FOOD00797)
Chinese water chestnut (FooDB: FOOD00332)
Nopal (FooDB: FOOD00416)
Carob (FooDB: FOOD00321)
Agave (FooDB: FOOD00563)
Narrowleaf cattail (FooDB: FOOD00564)
Giant butterbur (FooDB: FOOD00314)
Sesbania flower (FooDB: FOOD00469)

Stalk vegetable

Brassica

Brassicas (FooDB: FOOD00857)

Cereal and cereal product

Other bread

Other bread (FooDB: FOOD00269)

Cereal

Cereal product

Dough

Sourdough (FooDB: FOOD00275)

Cereals and cereal products (FooDB: FOOD00858)

Pulse

Bean

Lentil

Lentils (FooDB: FOOD00098)

Pea

Other pulse

White lupine (FooDB: FOOD00403)
Lupine (FooDB: FOOD00104)

Pulses (FooDB: FOOD00867)

Soy

Soy bean (FooDB: FOOD00085)

Soy product

Other soy product (FooDB: FOOD00271)

Abalone (FooDB: FOOD00279)
Conch (FooDB: FOOD00611)

Gourd

Chayote (FooDB: FOOD00325)
Cucumber (FooDB: FOOD00065)
Muskmelon (FooDB: FOOD00064)
Cucurbita (FooDB: FOOD00066)
Watermelon (FooDB: FOOD00052)
Bitter gourd (FooDB: FOOD00115)
Calabash (FooDB: FOOD00318)
Towel gourd (FooDB: FOOD00492)
Winter squash (FooDB: FOOD00283)
Butternut squash (FooDB: FOOD00317)
Wax gourd (FooDB: FOOD00499)
Green zucchini (FooDB: FOOD00875)
Yellow zucchini (FooDB: FOOD00876)
Japanese pumpkin (FooDB: FOOD00886)
Sunburst squash (pattypan squash) (FooDB: FOOD00874)
Tinda (FooDB: FOOD00559)
Horned melon (FooDB: FOOD00761)

Tea

Herbal tea

Greenthread tea (FooDB: FOOD00820)

Cocoa and cocoa product

Cocoa

Cocoa bean (FooDB: FOOD00182)

Fat and oil

Fats and oils (FooDB: FOOD00864)

Synthetic

Personal care products

Personal care products (HMDB: HMDB0035155)

Process

Naturally occurring process

Biological process

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0035155)

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0035155)

Cellular process

Cell signaling (HMDB: HMDB0035155)

Biochemical process

Lipid transport (HMDB: HMDB0035155)

Role

Industrial application

Personal care product

Personal care product (HMDB: HMDB0035155)

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0035155)

Coloring agent

Fluorescent agent

Expectorant (HMDB: HMDB0035155)
Sedative (HMDB: HMDB0035155)

Agriculture

Pesticide

Pesticide (HMDB: HMDB0035155)

Pharmaceutical industry

Antineoplastic agent

Antitumor (HMDB: HMDB0035155)
Cancer preventive (HMDB: HMDB0035155)

Antimicrobial agent

Ascaricide (HMDB: HMDB0035155)

Central nervous system stimulant (HMDB: HMDB0035155)
Fragrance (HMDB: HMDB0035155)

Food and nutrition

Food additive

Flavoring agent

Flavor (HMDB: HMDB0035155)
Flavoring Agent (HMDB: HMDB0035155)

Biological role

Physical Properties

State

Liquid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	< -15 °C	Not Available
Boiling Point	229.00 to 230.00 °C. @ 760.00 mm Hg	The Good Scents Company Information System
Water Solubility	0.1 mg/mL at 25 °C	Not Available
LogP	3.56	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	1.37 g/L	ALOGPS
logP	2.89	ALOGPS
logP	2.5	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	16.33	ChemAxon
pKa (Strongest Basic)	-2.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	51.18 m³·mol⁻¹	ChemAxon
Polarizability	19.67 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	139.668	31661259
DarkChem	[M-H]-	132.786	31661259
DeepCCS	[M+H]+	138.055	30932474
DeepCCS	[M-H]-	134.486	30932474
DeepCCS	[M-2H]-	171.696	30932474
DeepCCS	[M+Na]+	147.097	30932474
AllCCS	[M+H]+	136.7	32859911
AllCCS	[M+H-H2O]+	132.7	32859911
AllCCS	[M+NH4]+	140.5	32859911
AllCCS	[M+Na]+	141.6	32859911
AllCCS	[M-H]-	137.7	32859911
AllCCS	[M+Na-2H]-	139.7	32859911
AllCCS	[M+HCOO]-	142.0	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
beta-Geraniol	CC(C)=CCC\C(C)=C\CO	1835.5	Standard polar	33892256
beta-Geraniol	CC(C)=CCC\C(C)=C\CO	1226.4	Standard non polar	33892256
beta-Geraniol	CC(C)=CCC\C(C)=C\CO	1249.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
beta-Geraniol,1TMS,isomer #1	CC(C)=CCC/C(C)=C/CO[Si](C)(C)C	1341.9	Semi standard non polar	33892256
beta-Geraniol,1TBDMS,isomer #1	CC(C)=CCC/C(C)=C/CO[Si](C)(C)C(C)(C)C	1559.6	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental GC-MS	GC-MS Spectrum - beta-Geraniol GC-MS (1 TMS)	splash10-002f-9800000000-16b748da465c428492a4	2014-06-16	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - beta-Geraniol EI-B (Non-derivatized)	splash10-014l-9000000000-25934c23f4bc9ba87142	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - beta-Geraniol EI-B (Non-derivatized)	splash10-014i-9000000000-a4d79e7813b94cf0d54b	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - beta-Geraniol EI-B (Non-derivatized)	splash10-014i-9100000000-3a5359aae818f9966cbd	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - beta-Geraniol EI-B (Non-derivatized)	splash10-00kf-9200000000-4a8a23071f388f446451	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - beta-Geraniol EI-B (Non-derivatized)	splash10-014i-9100000000-f24e92e3c3efdc35a606	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - beta-Geraniol EI-B (Non-derivatized)	splash10-014i-9100000000-d8e4f64753ef594f6d40	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - beta-Geraniol EI-B (Non-derivatized)	splash10-014l-9000000000-2bce8c0905dd12aa5dac	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - beta-Geraniol GC-MS (Non-derivatized)	splash10-002f-9800000000-16b748da465c428492a4	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - beta-Geraniol GC-EI-TOF (Non-derivatized)	splash10-0006-4900000000-7e43c8601ed65028cae5	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - beta-Geraniol GC-MS (Non-derivatized) - 70eV, Positive	splash10-014u-9300000000-c85bc4c928fbf7d824e8	2016-09-22	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - beta-Geraniol GC-MS (1 TMS) - 70eV, Positive	splash10-030c-9520000000-69b7fbbb25764f7b612e	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - beta-Geraniol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - beta-Geraniol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
MS	Mass Spectrum (Electron Ionization)	splash10-014l-9100000000-f59382e51acd0b540204	2014-09-20	Not Available	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol n/a 10V, negative-QTOF	splash10-0a4i-1900000000-710389d2548f45d60502	2020-07-21	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol QTOF 4V, positive-QTOF	splash10-001r-9500000000-d864036a8f8b4cdb20ae	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol QTOF 5V, positive-QTOF	splash10-001r-9400000000-e3661fd0b608943d6b6c	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol QTOF 7V, positive-QTOF	splash10-001i-9200000000-d748b4cd92b7c69ffee3	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol QTOF 10V, positive-QTOF	splash10-001i-9100000000-b6abc8d3af3aa99879b4	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol QTOF 15V, positive-QTOF	splash10-001i-9000000000-710e0ba546f9b86b8e40	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol QTOF 17V, positive-QTOF	splash10-001i-9000000000-4cc179896d0516270659	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol QTOF 20V, positive-QTOF	splash10-001i-9000000000-7f3a48636d9da2cda821	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol QTOF 23V, positive-QTOF	splash10-001i-9000000000-4b196d3d8e84ecd0e9f3	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol QTOF 25V, positive-QTOF	splash10-003r-9000000000-718f1d4e975f4b2446d1	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol QTOF 27V, positive-QTOF	splash10-003u-9000000000-2e43acc8a377504a4329	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol QTOF 30V, positive-QTOF	splash10-005c-9000000000-fe7ffaf2c7e121c33b7c	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol QTOF 33V, positive-QTOF	splash10-005c-9000000000-467c307d1f0822b86ea0	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol QTOF 35V, positive-QTOF	splash10-005c-9000000000-5939202301ea6107df2c	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol QTOF 40V, positive-QTOF	splash10-002f-9000000000-0e13687577d30f6265cc	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol QTOF 45V, positive-QTOF	splash10-0f96-9000000000-e478c8b2587c1134117d	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol Orbitrap 1V, positive-QTOF	splash10-000i-1900000000-5f3fc91bdf843e40a266	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol Orbitrap 1V, positive-QTOF	splash10-000i-1900000000-ab16b7d86a06d659d4f3	2020-07-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - beta-Geraniol Orbitrap 2V, positive-QTOF	splash10-000i-3900000000-4dd10bbea41237cba535	2020-07-22	HMDB team, MONA	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Geraniol 10V, Positive-QTOF	splash10-0a4r-1900000000-3d437630e5bec67a7e07	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Geraniol 20V, Positive-QTOF	splash10-052r-8900000000-0e505c85cec6344cab5c	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Geraniol 40V, Positive-QTOF	splash10-0gb9-9100000000-c7400df359a9559bd594	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Geraniol 10V, Negative-QTOF	splash10-0udi-0900000000-113756054eed13d33ee4	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Geraniol 20V, Negative-QTOF	splash10-0fk9-0900000000-dea43b41c5b791cef9d2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - beta-Geraniol 40V, Negative-QTOF	splash10-0aou-9800000000-c028a2bd655026094251	2016-08-03	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View

IR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M-H]-)	2023-02-04	FELIX lab	View Spectrum
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)	2023-02-04	FELIX lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Saliva

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Saliva	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Not Specified	Normal	24421258	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Geraniol

METLIN ID

Not Available

PubChem Compound

637566

PDB ID

Not Available

ChEBI ID

17447

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1006992

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
Turner CE, Elsohly MA, Boeren EG: Constituents of Cannabis sativa L. XVII. A review of the natural constituents. J Nat Prod. 1980 Mar-Apr;43(2):169-234. doi: 10.1021/np50008a001. [PubMed:6991645 ]
McGarvey DJ, Croteau R: Terpenoid metabolism. Plant Cell. 1995 Jul;7(7):1015-26. doi: 10.1105/tpc.7.7.1015. [PubMed:7640522 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for beta-Geraniol (HMDB0035155)

MOL for HMDB0035155 (beta-Geraniol)

3D MOL for HMDB0035155 (beta-Geraniol)

3D SDF for HMDB0035155 (beta-Geraniol)

3D-SDF for HMDB0035155 (beta-Geraniol)

PDB for HMDB0035155 (beta-Geraniol)

3D PDB for HMDB0035155 (beta-Geraniol)

SMILES for HMDB0035155 (beta-Geraniol)

INCHI for HMDB0035155 (beta-Geraniol)

Structure for HMDB0035155 (beta-Geraniol)

3D Structure for HMDB0035155 (beta-Geraniol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

IR Spectra