1,3-octane diol
1,3-propanediol, 1-pentyl-
 
Notes:
None found
Synonyms   Articles   Notes   Search
CAS Number: 23433-05-8Picture of molecule3D/inchi
Nikkaji Web: J103.153H
Beilstein Number: 2069738
MDL: MFCD01711163
XlogP3-AA: 1.60 (est)
Molecular Weight: 146.22986000
Formula: C8 H18 O2
NMR Predictor: Predict (works with chrome or firefox)
EFSA/JECFA Comments: Racemate.
Category: flavoring 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
PubMed: Search
NCBI: Search
DG SANTE Food Flavourings: 02.198  octane-1,3-diol
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: colorless clear liquid (est)
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 0.98000 to 0.98600 @  25.00 °C.
Pounds per Gallon - (est).: 8.155 to  8.205
Refractive Index: 1.45200 to 1.45800 @  20.00 °C.
Boiling Point: 254.00 to  256.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.002000 mmHg @ 25.00 °C. (est)
Flash Point: 243.00 °F. TCC ( 117.22 °C. )
logP (o/w): 1.298 (est)
Soluble in:
 alcohol
 water, slightly
 water, 2933 mg/L @ 25 °C (est)
Insoluble in:
 water
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: musty
 
Odor Description:
musty
 
 
Flavor Type: bitter
 
 bitter  
Taste Description:
bitter
 
Odor and/or flavor descriptions from others (if found).
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
None found
Synonyms   Articles   Notes   Search   Top
Suppliers:
Sigma-Aldrich
For experimental / research use only.
1,3-Octanediol analytical standard
Chemical Sources Association
Need This Item for Flavor/Food?: You can contact the CSA
Synonyms   Articles   Notes   Search   Top
Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-rat LD50  > 20000 mg/kg
(Frankenfeld et al., 1975)

oral-rat LD50  > 20000 mg/kg
Journal of Agricultural and Food Chemistry. Vol. 23, Pg. 418, 1975.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: flavoring agents
Recommendation for 1,3-octane diol usage levels up to:
 not for fragrance use.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.0012 (μg/capita/day)
Modified Theoretical Added Maximum Daily Intake (mTAMDI): 3900 (μg/person/day)
Threshold of Concern:1800 (μg/person/day)
Structure Class: I
 
Food categories according to Commission Regulation EC No. 1565/2000 (EC, 2000) in FGE.06 (EFSA, 2002a). According to the Industry the "normal" use is defined as the average of reported usages and "maximum use" is defined as the 95th percentile of reported usages (EFSA, 2002i).
Note: mg/kg = 0.001/1000 = 0.000001 = 1/1000000 = ppm.
 average usage mg/kgmaximum usage mg/kg
Dairy products, excluding products of category 02.0 (01.0): 7.0000035.00000
Fats and oils, and fat emulsions (type water-in-oil) (02.0): 5.0000025.00000
Edible ices, including sherbet and sorbet (03.0): 10.0000050.00000
Processed fruit (04.1): 7.0000035.00000
Processed vegetables (incl. mushrooms & fungi, roots & tubers, pulses and legumes), and nuts & seeds (04.2): --
Confectionery (05.0): 10.0000050.00000
Chewing gum (05.0): --
Cereals and cereal products, incl. flours & starches from roots & tubers, pulses & legumes, excluding bakery (06.0): 5.0000025.00000
Bakery wares (07.0): 10.0000050.00000
Meat and meat products, including poultry and game (08.0): 2.0000010.00000
Fish and fish products, including molluscs, crustaceans and echinoderms (MCE) (09.0): 2.0000010.00000
Eggs and egg products (10.0): --
Sweeteners, including honey (11.0): --
Salts, spices, soups, sauces, salads, protein products, etc. (12.0): 5.0000025.00000
Foodstuffs intended for particular nutritional uses (13.0): 10.0000050.00000
Non-alcoholic ("soft") beverages, excl. dairy products (14.1): 5.0000025.00000
Alcoholic beverages, incl. alcohol-free and low-alcoholic counterparts (14.2): 10.0000050.00000
Ready-to-eat savouries (15.0): 20.00000100.00000
Composite foods (e.g. casseroles, meat pies, mincemeat) - foods that could not be placed in categories 01.0 - 15.0 (16.0): 5.0000025.00000
Synonyms   Articles   Notes   Search   Top
Safety References:
European Food Safety Athority(EFSA): Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...
European Food Safety Authority (EFSA) reference(s):
Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC) on a request from the Commission related to - Flavouring Group Evaluation 10: Aliphatic primary and secondary saturated and unsaturated alcohols, aldehydes, acetals, carboxylic acids and esters containing an additional oxygenated functional group and lactones from chemical groups 9, 13 and 30 - (Commission Regulation (EC) No 1565/2000 of 18 July 2000)
View page or View pdf
Flavouring Group Evaluation 10, Revision 1 (FGE10 Rev1)[1] - Aliphatic primary and secondary saturated and unsaturated alcohols, aldehydes, acetals, carboxylic acids and esters containing an additional oxygenated functional group and lactones from chemical groups 9, 13 and 30 - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food (AFC)
View page or View pdf
Flavouring Group Evaluation 64 (FGE.64): Consideration of aliphatic acyclic diols, triols, and related substances evaluated by JECFA (57th meeting) structurally related to aliphatic primary and secondary saturated and unsaturated alcohols, aldehydes, acetals, carboxylic acids and esters containing an additional oxygenated functional group and lactones from chemical groups 9, 13 and 30 evaluated by EFSA in FGE.10Rev1 (EFSA, 2008ab)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 92 (FGE.92): Consideration of aliphatic acyclic diols, triols, and related substances evaluated by JECFA (68th meeting) structurally related to aliphatic primary and secondary saturated and unsaturated alcohols, aldehydes, acetals, carboxylic acids and esters containing an additional oxygenated functional group and lactones evaluated by EFSA in FGE.10Rev1 (2009)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 10, Revision 2 (FGE.10Rev2): Aliphatic primary and secondary saturated and unsaturated alcohols, aldehydes, acetals, carboxylic acids and esters containing an additional oxygenated functional group and lactones from chemical groups 9, 13 and 30
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 10, Revision 3 (FGE.10Rev3): Aliphatic primary and secondary saturated and unsaturated alcohols, aldehydes, acetals, carboxylic acids and esters containing an additional oxygenated functional group and lactones from chemical groups 9, 13 and 30
View page or View pdf
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 90927
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 octane-1,3-diol
Chemidplus: 0023433058
Synonyms   Articles   Notes   Search   Top
References:
 octane-1,3-diol
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 90927
Pubchem (sid): 135048980
Pherobase: View
Synonyms   Articles   Notes   Search   Top
Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (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): HMDB29359
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
No odor group found for these
 gentiana lutea root extractFL/FR
 prunus serotina bark extractFL/FR
aldehydic
 citronellyl oxyacetaldehydeFL/FR
 tridecanalFL/FR
balsamic
 peru balsam oilFL/FR
 peru balsam resinoidFL/FR
 terpinyl isovalerateFL/FR
caramellic
 fenugreek oleoresinFL/FR
 immortelle absoluteFL/FR
chocolate
 cocoa hexenalFL/FR
 cocoa oleoresinFL/FR
citrus
2-heptanolFL/FR
(+)-nootkatoneFL/FR
bitter orange peel oil brazilFL/FR
cocoa
 theobroma cacao extractFL/FR
coffee
 coffea arabica seed extractFL/FR
roasted arabica coffee bean oilFL/FR
fatty
(E,Z,Z)-2,4,7-tridecatrienalFL/FR
floral
(Z)-jasmoneFL/FR
 nerolFL/FR
 terpinyl valerateFL/FR
hay
 tobacco leaf absoluteFL/FR
herbal
black camellia sinensis leaf infusionFL/FR
 levisticum officinale root extractFL/FR
incense
 frankincense gum papyriferaFL/FR
musk
dextro,laevo-musconeFL/FR
powdery
 dibenzyl ketoneFL/FR
tea
 camellia oleifera leaf extractFL/FR
 
For Flavor
 
balsamic
 peru balsam oilFL/FR
 peru balsam resinoidFL/FR
bitter
2-acetyl-5-methyl pyrroleFL
 amarogentinFL
 cocoa pyrazines base (mixture of pyrazines)FL
 dibenzyl ketoneFL/FR
3,4-dihydroxybenzaldehydeFL
 frankincense gum papyriferaFL/FR
 glyceryl tributyrateFL
 methyl ethoxypyrazineFL
 paullinia cupana seed extractFL
 terpin anhydrousFL
 terpinyl isovalerateFL/FR
 theobromineFL
(E,Z,Z)-2,4,7-tridecatrienalFL/FR
brown
 fenugreek oleoresinFL/FR
 juglans nigra shell extractFL
chocolate
bitter chocolate flavorFL
bittersweet chocolate flavorFL
 cocoa oleoresinFL/FR
citrus
 citronellyl oxyacetaldehydeFL/FR
bitter lemon flavorFL
 nerolFL/FR
(+)-nootkatoneFL/FR
bitter orange flavorFL
cocoa
 cocoa distillatesFL
 cocoa hexenalFL/FR
 theobroma cacao extractFL/FR
coffee
 coffea arabica seed extractFL/FR
cooling
(2S,5R)-N-[4-(2-amino-2-oxoethyl)phenyl]-5-methyl-2-(propan-2-yl)cyclohexanecarboxamideFL
fruity
2-heptanolFL/FR
bitter orange peel oil brazilFL/FR
 prunus serotina bark extractFL/FR
 terpinyl valerateFL/FR
grassy
 tobacco leaf absoluteFL/FR
green
 gentiana lutea root extractFL/FR
 immortelle absoluteFL/FR
herbal
black camellia sinensis leaf infusionFL/FR
musk
dextro,laevo-musconeFL/FR
nutty
 peanut oxazoleFL
roasted
 acer spicatum bark extractFL
roasted arabica coffee bean oilFL/FR
spicy
 levisticum officinale root extractFL/FR
sulfurous
2-methyl thiopheneFL
tea
 camellia oleifera leaf extractFL/FR
waxy
 tridecanalFL/FR
woody
 ginseng distillatesFL
(Z)-jasmoneFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
None Found
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 apple fruit - up to 21 mg/kg
Search  PMC Picture
 apple juice - up to 95.1 mg/kg
Search  PMC Picture
 pear fruit
Search Trop  Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
 octane-1,3-diol
1,3-octanediol
 propane-1,3-diol, 1-pentyl-
1,3-propanediol, 1-pentyl-
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: Matrix-assisted laser desorption/ionization mass spectrometric analysis of aliphatic biodegradable photoluminescent polymers using new ionic liquid matrices.
PubMed: A novel method for the determination of total 1,3-octanediols in apple juice via 1,3-dioxanes by solid-phase microextraction and high-speed gas chromatography.
PubMed: More than a protective group: synthesis and applications of a new chiral silane.
PubMed: Novel 1,3-dioxanes from apple juice and cider.
PubMed: Metabolic profile of linoleic acid in stored apples: formation of 13(R)-hydroxy-9(Z),11(E)-octadecadienoic acid.
PubMed: Biosynthesis of R-(+)-octane-1,3-diol. Crucial role of beta-oxidation in the enantioselective generation of 1,3-diols in stored apples.
PubMed: Isolation, identification, and enantioselective synthesis of octane-1,3,7-triol: determination of its absolute configuration
PubMed: Absolute configuration of octanol derivatives in apple fruits.
Synonyms   Articles   Notes   Search   Top
Please share your Comments.
Email Address:
 
 
 
 
Top of Page Home
Copyright © 1980-2021 Perflavory ™ Disclaimer Privacy Policy