jasmin cyclopentanol
 
Right Click Picture For More Options. (Safari 1.2 (v125) Compatible).
 
IUPAC name :2-[(E)-hex-2-enyl]cyclopentan-1-ol
InChI :InChI=1/C11H20O/c1-2-3-4-5-7-10-8-6-9-11(10)12/h4-5,10-12H,2-3,6-9H2,1H3/b5-4+
InChIKey :OLPVLAJYJZWXPZ-SNAWJCMRBN
SMILES :CCC\C=C\CC1CCCC1O
cas number :34686-67-4
molar refractivity :52.56 ± 0.3 cm3
parachor :4337.3 ± 4.0 cm3
index of refraction :1.486 ± 0.02
surface tension :32.6 ± 3.0 dyne/cm
density :0.919 ± 0.06 g/cm3
polarizability :20.83 ± 0.5 10-24cm3
xlogp : 3.40
molecular weight : 168.2759000
formula :C11 H20 O
 
 
export tariff code :2906.19.5000
fda reg :unspecified
 

Suppliers :
Bedoukian Research :JASMONOL
≥97.0%, Kosher

organoleptics :
odor type :floral
odor strength :medium
odor description :
at 100.00 %.  
floral green fresh natural waxy jasmin
substantivity :112  Hour(s)

properties :
appearence :colorless clear liquid
assay : 97.00 to 100.00 %   sum of isomers
Food Chemicals Codex Listed :No
specific gravity :0.90000 to 0.92000 @ 25.00 °C.
pounds per gallon - calc. : 7.489 to 7.655
refractive index :1.46500 to 1.48000 @ 20.00 °C.
boiling point : 85.00 °C. @ 2.00 mm Hg
logp : 3.42

safety :
most important hazard(s) : Xi - Irritant
Oral Toxicity(LD50) : Not determined
Dermal Toxicity(LD50) : Not determined
flash point ( Deg. F. ) : 200.00  °F.  TCC  ( 93.33 °C. )
recommendation for jasmin cyclopentanol usage levels up to :
  6.0000 % in the fragrance concentrate.
recommendation for jasmin cyclopentanol usage levels up to :
 not for flavor use.

safety references :
EPI System :view
 
 
 2-[(E)-hex-2-enyl]cyclopentan-1-ol
chemidplus :034686674
EPA Substance Registry Services :34686-67-4
NLM Chemical Carcinogenesis Research Information System :34686-67-4
NLM Developmental and Reproductive Toxicity :34686-67-4
NLM Env. Mutagen Info. Center :34686-67-4
NLM GENetic TOXicology :34686-67-4

references :
 2-[(E)-hex-2-enyl]cyclopentan-1-ol
pubchem :694892

other :
synonyms :
2-hexen-1-yl cyclopentanole
2-hexenyl cyclopentanol
2-(2-hexenyl) cyclopentanol
2-(2-hexenyl)cyclopentanole
 jasmin cyclopentanol
 jasmonol

soluble in :
 alcohol

insoluble in :
 water

(odor and/or flavor) blends with :
isoamyl phenyl acetate
isoamyl salicylate
 amyris wood oil
para-anisyl alcohol
isobutyl salicylate
 cedarwood oils
 citronella oil
 decanol
9-decen-1-ol
 dihydrojasmone
 dihydromyrcenol
 dimethyl benzyl carbinyl butyrate
 floral pyranol
 geranium oil
 hexyl 2-methyl butyrate
 hexyl tiglate
 labdanum resinoid
laevo-linalool
 melon heptenal
 methyl dihydrojasmonate
 musks
 nerolidol
 nonanal
(Z)-6-nonen-1-al
 nutmeg oil
 ocean propanal
gamma-octalactone
 octanol
 orange oil
 orangeflower absolute
 patchouli ethanone
 petitgrain oil
 phenyl acetaldehyde dimethyl acetal
 rose butanoate
 santall
 tangerine oil
 vetiver oil
 violet leaf absolute
 watermelon ketone
 woody acetate

(odor and/or flavor) used in :
 acacia
 amber
 apricot
 bayberry
 bouquet
 cedarwood
 cheese blue cheese
 citrus
 cranberry
 dairy
 floral
 gardenia
 grapefruit
 grass sweet grass
 herbal
 honeysuckle chevrefeuille
 jasmin
 juniperberry
 lemon
 lilac lilas syringa
 lily
 melon
 melon watermelon muskmelon cantaloupe
 milk
 muguet lily of the valley
 neroli
 oakmoss mousse de chene
 orange
 orange bitter orange
 orange blossom fleur d'oranger
 orchid
 orris iris
 peach
 pineapple
 poppy red poppy
 rain
 reseda mignonette
 rose
 rose d'orient
 rose red rose
 rose white rose
 strawberry
 tea green tea
 tuberose tubereuse
 waxy
 woody

natural occurrence in :
not found in nature



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