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indolall
indolam 50 (IFF)

Sponsors

Fragrance Demo Formulas
Name:7-hydroxy-3,7-dimethyloctanal; 1H-indole
CAS Number: 68908-82-7Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:272-683-5
Molecular Weight:289.41859000
Formula:C18 H27 N O2
NMR Predictor:Predict (works with chrome or firefox)
Name:8,8-di(indol-1-yl)-2,6-dimethyloctan-2-ol
CAS Number: 67801-36-9Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:267-156-1
Nikkaji Web:J317.159K
XlogP3-AA:6.30 (est)
Molecular Weight:388.55424000
Formula:C26 H32 N2 O
NMR Predictor:Predict (works with chrome or firefox)
Category:fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist:Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
 
Physical Properties:
Appearance:yellow to amber viscous liquid (est)
Assay: 98.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 251.60 °C. @ 760.00 mm Hg (est)
Vapor Pressure:0.003180 mm/Hg @ 25.00 °C. (est)
Flash Point: 219.00 °F. TCC ( 103.80 °C. ) (est)
logP (o/w): 1.539 (est)
Soluble in:
 alcohol
 water, 2.854 mg/L @ 25 °C (est)
Insoluble in:
 water
Stability:
 alcoholic lotion
 antiperspirant
 deo stick
 detergent
 fabric softener
 hard surface cleaner
 shampoo
 soap
 
Organoleptic Properties:
Odor Type: animal
Odor Strength:high ,
recommend smelling in a 1.00 % solution or less
Substantivity:340 hour(s) at 10.00 %
animal fecal jasmin
Odor Description:at 1.00 % in dipropylene glycol. animal fecal indole
Luebke, William tgsc, (1996)
Odor sample from: International Flavors & Fragrances Inc.
Odor and/or flavor descriptions from others (if found).
IFF
Indolene 50% BB
Odor Description:A floral, jasmin note with slight animalic character which is useful in extending natural absolute Jasmin
Modified animal, fecal note useful in floral absolute types. Increases the substantivity of a fragrance and provides fixation as well as floralcy.
PerfumersWorld
Indolene
Odor Description:strong narcotic-floral moth ball naphthelene erogenic-floral animal jasmine orange-flower
Blends-well-with - White Florals
IFF
Indolene 50% DEP
Odor Description:A floral, jasmin note with slight animalic character which is useful in extending natural absolute Jasmin
Robertet
Schiff indol hydroxy 50 rh
Odor Description:Floral, white flower, sweet
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: perfuming agents
 
Suppliers:
Azelis UK
INDOLENE 50 PCT DEP
Services
Berjé
Indolene
Happening at Berje
CG Herbals
Indolene 50% / Castor Oil
Odor: Animal, Fecal, Indole
CG Herbals
Schiff's Base Indolene
Charabot
Schiff indol hydroxy 50 rh
Odor: Floral, white flower, sweet
Ernesto Ventós
INDOLEN 50
Odor: ANIMAL, FLORAL, JASMINE
IFF
Indolene 50% BB
Odor: A floral, jasmin note with slight animalic character which is useful in extending natural absolute Jasmin
Use: Modified animal, fecal note useful in floral absolute types. Increases the substantivity of a fragrance and provides fixation as well as floralcy.
IFF
Indolene 50% DEP
Odor: A floral, jasmin note with slight animalic character which is useful in extending natural absolute Jasmin
Lluch Essence
SCHIFF BASE INDOLE/HYDROXYCITRONELLAL 50%
Penta International
INDOLENE 50
PerfumersWorld
Indolene
Odor: strong narcotic-floral moth ball naphthelene erogenic-floral animal jasmine orange-flower
Use: Blends-well-with - White Florals
Perfumery Laboratory
INDOLENE 50
Odor: Inol, jasmine with fecal note
Robertet
Schiff indol hydroxy 50 rh
Odor: Floral, white flower, sweet
Taytonn
Indolene 50
Odor: Animalic/ Animal, Floral
The John D. Walsh Company
Indolene 50
The Perfumers Apprentice
Indolene 50 (I)
Odor: Floral, Jasmin, Animal
Use: Modified animal, fecal note useful in floral absolute types. Increases the substantivity of a fragrance and provides fixation as well as floralcy.
Vigon International
Indolene 50% (Indole/Hydroxycitronellal Schiff Base)
Odor: ANIMALISTIC, FLORAL WARM
 
Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
Acute toxicity, Oral (Category 4), H302
Skin irritation (Category 2), H315
Skin sensitisation (Category 1), H317
Serious eye damage/eye irritation (Category 2A), H320
GHS Label elements, including precautionary statements
 
Pictogramexclamation-mark.jpg
 
Signal word Warning
Hazard statement(s)
H302 - Harmful if swallowed
H315 - Causes skin irritation
H317 - May cause an allergic skin reaction
H320 - Causes eye irritation
Precautionary statement(s)
P102 - Keep out of reach of children.
P103 - Read label before use
P261 - Avoid breathing dust/fume/gas/mist/vapours/spray.
P264 - Wash skin thouroughly after handling.
P270 - Do not eat, drink or smoke when using this product.
P280 - Wear protective gloves/protective clothing/eye protection/face protection.
P301 + P312 - IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P302 + P352 - IF ON SKIN: wash with plenty of soap and water.
P330 - Rinse mouth.
P337 + P313 - IF eye irritation persists: Get medical advice/attention.
P501 - Dispose of contents/ container to an approved waste disposal plant.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category: fragrance agents
Recommendation for indolall usage levels up to:
  5.0000 % in the fragrance concentrate.
 
Recommendation for indolall flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
EPA Substance Registry Services (TSCA):68908-82-7
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :163281
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:2
7-hydroxy-3,7-dimethyloctanal; 1H-indole
Chemidplus:0068908827
8,8-di(indol-1-yl)-2,6-dimethyloctan-2-ol
Chemidplus:067801369
 
References:
 7-hydroxy-3,7-dimethyloctanal; 1H-indole
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:68908-82-7
Pubchem (cid):163281
Pubchem (sid):135120206
 8,8-di(indol-1-yl)-2,6-dimethyloctan-2-ol
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:67801-36-9
Pubchem (cid):106826
Pubchem (sid):684048
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2009
(IUPAC):Atomic Weights of the Elements 2009 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
HMDB (The Human Metabolome Database):Search
ChemSpider:View
 
Potential Blenders and core components note
For Odor
aldehydic
dodecanal (aldehyde C-12 lauric)
FL/FR
nonanal (aldehyde C-9)
FL/FR
10-
undecenal (aldehyde C-11 undecylenic)
FL/FR
amber
ambroxan
FL/FR
cistus ladaniferus resinoid
FR
animal
animal carbolactone
FR
iso
butyl quinoline
FR
civet absolute
FL/FR
para-
cresyl caprylate
FL/FR
para-
cresyl isobutyrate
FL/FR
para-
cresyl phenyl acetate
FL/FR
ethyl 4-methyl salicylate
FL/FR
indocolore (Firmenich)
FR
indole
FL/FR
anisic
para-
anisaldehyde
FL/FR
balsamic
amyris wood oil
FL/FR
siam
benzoin resinoid
FL/FR
benzyl benzoate
FL/FR
benzyl salicylate
FL/FR
iso
butyl cinnamate
FL/FR
cinnamyl alcohol
FL/FR
clover nitrile
FR
ethyl cinnamate
FL/FR
fir balsam absolute
FR
methyl (E)-cinnamate
FL/FR
myrrh oil
FL/FR
3-
phenyl propyl alcohol
FL/FR
berry
raspberry ketone
FL/FR
fatty
coconut absolute
FL/FR
decanol
FL/FR
floral
alpha-
amyl cinnamaldehyde
FL/FR
iso
amyl salicylate
FL/FR
benzyl alcohol
FL/FR
bois de rose oil brazil
FL/FR
citronellol
FL/FR
coriander seed oil
FL/FR
para-
cresyl acetate
FL/FR
cyclamen aldehyde
FL/FR
cyclohexyl ethyl alcohol
FL/FR
9-
decen-1-ol
FL/FR
dimethyl anthranilate
FL/FR
dimethyl benzyl carbinol
FL/FR
ethyl phenyl acetate
FL/FR
floral pyranol
FR
geraniol
FL/FR
geranyl acetate
FL/FR
heliotropin
FL/FR
(Z)-3-
hexen-1-yl salicylate
FL/FR
alpha-
hexyl cinnamaldehyde
FL/FR
hyacinth ether
FR
hydroxycitronellal
FL/FR
leerall
FR
laevo-
linalool
FL/FR
linalool
FL/FR
linalool oxide
FL/FR
para-
methyl acetophenone
FL/FR
methyl dihydrojasmonate
FL/FR
nerol
FL/FR
nerolidol
FL/FR
neryl acetate
FL/FR
nonanol
FL/FR
ocean propanal
FL/FR
bitter
orangeflower absolute morocco
FL/FR
orris pyridine 25% IPM
FR
peony alcohol
FR
phenethyl alcohol
FL/FR
phenethyl phenyl acetate
FL/FR
phenethyl salicylate
FL/FR
rhodinol
FL/FR
rose butanoate
FL/FR
tetrahydrolinalool
FL/FR
fresh
10-
undecen-1-yl acetate
FL/FR
fruity
(E)-beta-
damascone
FL/FR
gamma-
undecalactone (aldehyde C-14 (so-called))
FL/FR
green
para-
dimethyl hydroquinone
FL/FR
diphenyl oxide
FL/FR
phenyl acetaldehyde dimethyl acetal
FL/FR
3-
phenyl propionaldehyde
FL/FR
hay
hay absolute
FR
herbal
carum carvi fruit oil
FL/FR
clary sage oil france
FL/FR
linalyl acetate
FL/FR
honey
methyl phenyl acetate
FL/FR
phenyl acetic acid
FL/FR
marine
marine pyridine
FR
mossy
oakmoss absolute
FL/FR
veramoss (IFF)
FR
musk
(Z)-
civet decenone
FL/FR
musk nonane
FR
naphthyl
beta-
naphthyl ethyl ether
FL/FR
powdery
para-
anisyl alcohol
FL/FR
spicy
benzyl isoeugenol
FL/FR
carnation absolute
FR
methyl isoeugenol
FL/FR
terpenic
alpha-
terpineol
FL/FR
tonka
coumarin
FR
tonka bean absolute
FR
waxy
ethyl laurate
FL/FR
woody
amber carbinol
FR
guaiacwood oil
FL/FR
gurjun balsam oil
FR
patchouli ethanone
FR
santall
FR
tobacarol (IFF)
FR
vetiver oil haiti
FL/FR
woody acetate
FR
(Z)-
woody amylene
FR
woody propanol
FR
For Flavor
No flavor group found for these
ethyl 4-methyl salicylate
FL/FR
methyl (E)-cinnamate
FL/FR
aldehydic
aldehydic
nonanal (aldehyde C-9)
FL/FR
animal
civet absolute
FL/FR
para-
cresyl caprylate
FL/FR
indole
FL/FR
aromatic
para-
cresyl acetate
FL/FR
para-
cresyl isobutyrate
FL/FR
balsamic
siam
benzoin resinoid
FL/FR
benzyl benzoate
FL/FR
benzyl salicylate
FL/FR
iso
butyl cinnamate
FL/FR
ethyl cinnamate
FL/FR
myrrh oil
FL/FR
berry
raspberry ketone
FL/FR
cherry
heliotropin
FL/FR
citrus
laevo-
linalool
FL/FR
linalool
FL/FR
nerol
FL/FR
alpha-
terpineol
FL/FR
creamy
para-
anisaldehyde
FL/FR
para-
methyl acetophenone
FL/FR
gamma-
undecalactone (aldehyde C-14 (so-called))
FL/FR
fatty
coconut absolute
FL/FR
10-
undecenal (aldehyde C-11 undecylenic)
FL/FR
floral
bois de rose oil brazil
FL/FR
citronellol
FL/FR
geraniol
FL/FR
linalyl acetate
FL/FR
methyl dihydrojasmonate
FL/FR
methyl phenyl acetate
FL/FR
neryl acetate
FL/FR
ocean propanal
FL/FR
bitter
orangeflower absolute morocco
FL/FR
phenethyl alcohol
FL/FR
phenyl acetic acid
FL/FR
rhodinol
FL/FR
tetrahydrolinalool
FL/FR
fruity
para-
anisyl alcohol
FL/FR
benzyl alcohol
FL/FR
(E)-beta-
damascone
FL/FR
dimethyl anthranilate
FL/FR
rose butanoate
FL/FR
greasy
10-
undecen-1-yl acetate
FL/FR
green
iso
amyl salicylate
FL/FR
cinnamyl alcohol
FL/FR
cyclamen aldehyde
FL/FR
cyclohexyl ethyl alcohol
FL/FR
para-
dimethyl hydroquinone
FL/FR
diphenyl oxide
FL/FR
geranyl acetate
FL/FR
(Z)-3-
hexen-1-yl salicylate
FL/FR
linalool oxide
FL/FR
nerolidol
FL/FR
oakmoss absolute
FL/FR
phenyl acetaldehyde dimethyl acetal
FL/FR
3-
phenyl propionaldehyde
FL/FR
herbal
carum carvi fruit oil
FL/FR
clary sage oil france
FL/FR
coriander seed oil
FL/FR
honey
ethyl phenyl acetate
FL/FR
phenethyl phenyl acetate
FL/FR
medicinal
dimethyl benzyl carbinol
FL/FR
phenethyl salicylate
FL/FR
musk
(Z)-
civet decenone
FL/FR
phenolic
para-
cresyl phenyl acetate
FL/FR
powdery
beta-
naphthyl ethyl ether
FL/FR
soapy
dodecanal (aldehyde C-12 lauric)
FL/FR
spicy
benzyl isoeugenol
FL/FR
methyl isoeugenol
FL/FR
3-
phenyl propyl alcohol
FL/FR
tropical
alpha-
amyl cinnamaldehyde
FL/FR
waxy
decanol
FL/FR
9-
decen-1-ol
FL/FR
ethyl laurate
FL/FR
alpha-
hexyl cinnamaldehyde
FL/FR
hydroxycitronellal
FL/FR
nonanol
FL/FR
woody
ambroxan
FL/FR
amyris wood oil
FL/FR
guaiacwood oil
FL/FR
vetiver oil haiti
FL/FR
 
Potential Uses:
FRanimal
 fixer
FRfloral
FRflower shop
FRhyacinth
FRjasmin
FRlilac
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
8,8-bis-(2,3-dihydroindol)-2,6-dimethyl-2-octanol
7-hydroxy-3,7-dimethyl octanal /indole
7-hydroxy-3,7-dimethyloctanal- 1H-indole(1:1)
7-hydroxy-3,7-dimethyloctanal; 1H-indole
 hydroxycitronellal indole condensation products
 hydroxycitronellal, indole condensation products
8,8-bis(1H-indol-1-yl)-2,6-dimethyl-2-octanol
beta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-1H-indole-1-heptanol
 indolall
 indolam 50 (IFF)
 indole hydroxycitronellal condensation products
 indole/ hydroxycitronellal schiff base
 indolene 50 (Givaudan)
 indolene 50% BB (IFF)
 indolene 50% DEP (IFF)
 indolyl trimethyl indole-1-heptanol
gamma-1H-indolyl-alpha,alpha,epslon-trimethyl-1H-indole-1-heptanol
 indolyl-trimethylindole-1-heptanol
 octanal, 7-hydroxy-3,7-dimethyl-, reaction products with 1H-indole
 

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