3,6-nonadien-1-ol
 
Right Click Picture For More Options. (Safari 1.2 (v125) Compatible).
 
IUPAC name :nona-3,6-dien-1-ol
InChI :InChI=1/C9H16O/c1-2-3-4-5-6-7-8-9-10/h3-4,6-7,10H,2,5,8-9H2,1H3
InChIKey :PICGPEBVZGCYBV-UHFFFAOYAS
SMILES :CCC=CCC=CCCO
(EINECS) number :278-518-3
cas number :76649-25-7
fema number :3884
coe number :10289
fl. number :02.189
molar refractivity :45.39 ± 0.3 cm3
parachor :381.3 ± 4.0 cm3
index of refraction :1.472 ± 0.02
surface tension :30.8 ± 3.0 dyne/cm
density :0.866 ± 0.06 g/cm3
polarizability :17.99 ± 0.5 10-24cm3
xlogp : 2.90
molecular weight : 140.2227400
formula :C9 H16 O
 
 
export tariff code :2905.29.9000
fda reg :unspecified
 

Suppliers :
Bedoukian Research :3,6-NONADIEN-1-OL BRI
≥92.0% (trans,cis), Kosher

organoleptics :
odor strength :high ,
recommend smelling in a 1.00 % solution or less
odor description :
at 1.00 % in dipropylene glycol.  
fresh green violet cucumber

properties :
appearence :colorless to pale yellow clear liquid
assay : 92.00 to 100.00 %   sum of isomers
Food Chemicals Codex Listed :No
boiling point : 214.00 to 215.00 °C. @ 760.00 mm Hg
logp : 2.69

safety :
Oral Toxicity(LD50) : Not determined
Dermal Toxicity(LD50) : Not determined
flash point ( Deg. F. ) : 184.00  °F.  TCC  ( 84.44 °C. )
recommendation for 3,6-nonadien-1-ol usage levels up to :
  1.0000 % in the fragrance concentrate.

safety references :
EPI System :view
 
 
 nona-3,6-dien-1-ol
(EINECS) number :278-518-3
chemidplus :076649257
EPA Substance Registry Services :76649-25-7
NLM Chemical Carcinogenesis Research Information System :76649-25-7
NLM Developmental and Reproductive Toxicity :76649-25-7
NLM Env. Mutagen Info. Center :76649-25-7
NLM GENetic TOXicology :76649-25-7

references :
 nona-3,6-dien-1-ol
fl. number :02.189
pubchem :743877

other :
synonyms :
 nona-3,6-dien-1-ol
3,6-nonadien-1-ol
3,6-nonadienol

soluble in :
 alcohol

insoluble in :
 water

(odor and/or flavor) blends with :
 cassie absolute
 cassie concrete
(Z)-3-hexen-1-yl (Z)-3-hexenoate
(Z)-3-hexen-1-yl methyl carbonate
 leaf acetal
 melon carboxaldehyde
 melon valerate
 methyl octine carbonate
(E,E)-2,6-nonadien-1-al
2,4-nonadien-1-al
(E,Z)-2,6-nonadien-1-al diethyl acetal
(E,Z)-2,6-nonadien-1-ol
(E,Z)-3,6-nonadien-1-ol
(Z,Z)-3,6-nonadien-1-ol
2,4-nonadien-1-ol
2,6-nonadien-1-ol
3,6-nonadien-1-ol
(E,Z)-3,6-nonadien-1-yl acetate
3,6-nonadien-1-yl acetate
2,4,6-nonatrien-1-al
(E)-2-nonen-1-al
(Z)-6-nonen-1-al
(E)-2-nonen-1-ol
(Z)-3-nonen-1-ol
2-nonyn-1-al dimethyl acetal
(E)-2-octen-1-al
 propyl 2,4-decadienoate
 violet decenol
 violet dienyne
 violet leaf absolute
 violet methyl carbonate
 violet nitrile
 watermelon ketone

(odor and/or flavor) used in :
 agrumen
 algae
 amaryllis
 apple green apple
 artichoke
 asafoetida
 asparagus
 avocado
 basil
 boronia
 boxwood
 boxwood blossom
 boxwoodberry
 cajuput
 carrot
 carrot seed
 cassie acacia farnesiana
 cassis black currant bud
 celery
 chamomile
 cilantro
 clary sage
 clematis
 cognac
 cortex
 costus
 cucumber
 daffodil narcissus
 dill
 dillenia
 elemi
 evergreen
 fennel
 fern fougere
 fig
 fir
 fir balsam
 foliage
 galbanum
 geranium
 grass
 grass green grass
 green
 guava
 hops houblon
 hugonia
 hyacinth jacinthe
 hydrangea
 iris blossom
 ivy leaf
 jonquil narcissus jonquilla
 leaf
 leaf green leaf
 lettuce
 liverwort
 lotus
 mango
 marjoram
 melon
 melon honeydew
 melon watermelon
 melon watermelon muskmelon cantaloupe
 mimosa wattle
 narcissus narcisse
 oregano
 orris iris
 pansy
 parsley
 pea green pea
 pear prickly pear
 pepper bell pepper
 petunia
 pine scotch pine
 privet
 privet blossom
 reseda mignonette
 rhubarb
 rootbeer
 rose geranium
 rose leaf
 stem
 strawberry leaf
 tomato
 tomato leaf
 valerian
 vegetable
 vegetation tropical hothouse vegetation
 vine
 violet
 violet leaf
 weedy
 wintergreen
 wormwood absinthium
 yew

natural occurrence in :
found in nature



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Html Last modified 11/29/2008