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General Material Information

Preferred name nonanol
Trivial Name 1-Nonanol
Short Description alcohol C9
Formula C9 H20 O
CAS Number 143-08-8
FEMA Number 2789
ECHA Number 205-583-7
FDA UNII NGK73Q6XMC
Nikkaji Number J2.549F
Beilstein Number 0969213
MDL MFCD00002990
COE Number 55
Bio Activity Summary External link
NMR Predictor External link
JECFA Food Flavoring 100 nonyl alcohol
FDA Patent No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm 143-08-8 ; NONYL ALCOHOL
Synonyms
  • alcohol C 9
  • alcohol C-9
  • alcohol C-9 10% dpg
  • alcohol C-9 FCC
  • alcohol C9
  • 1-hydroxynonane
  • nonalol
  • nonan-1-ol
  • N- nonan-1-ol
  • 1-nonanol
  • nonanol natural
  • nonanol, natural
  • nonyl alcohol
  • N- nonyl alcohol
  • nonyl alcohol 99%
  • nonylalkohol
  • octyl carbinol
  • pelargonalkohol
  • pelargonic alcohol
  • pelargyl alcohol
  • 1-Nonanol
  • n-Nonyl alcohol
  • n-Nonan-1-ol
  • 1-Hydroxynonane
  • NSC 5521
  • Linevol 9

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Literature & References

nonan-1-ol
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:143-08-8
Pubchem (cid):8914
Pubchem (sid):134973591
Flavornet:143-08-8
Pherobase:View
Publications by Info
Volatile Flavor Components in Bogyojosaeng and Suhong Cultivars of Strawberry (Fragaria ananassa Duch.)
Publications by PubMed
On the influence of column temperature on the isothermal retention indices of structurally different solutes on a poly(dimethylsiloxane) capillary column.
Predicted 3D structures of olfactory receptors with details of odorant binding to OR1G1.
Differential involvement of glutamate-gated chloride channel splice variants in the olfactory memory processes of the honeybee Apis mellifera.
A laboratory evaluation of alcohols as attractants for the sandfly Lutzomyia longipalpis (Diptera:Psychodidae).
Optimization of two different dispersive liquid-liquid microextraction methods followed by gas chromatography-mass spectrometry determination for polycyclic aromatic hydrocarbons (PAHs) analysis in water.
Characterization of volatile organic compounds emitted by barley (Hordeum vulgare L.) roots and their attractiveness to wireworms.
The adsorption kinetics of a fluorinated surfactant--heptadecafluoro-1-nonanol.
Petrodiesel-like straight chain alkane and fatty alcohol production by the microalga Chlorella sorokiniana.
Effect of the addition of alkanols of different topology to dipalmitoyl-phosphatidylcholine vesicles in the presence of gramicidin.
Label-free capacitive DNA sensor using immobilized pyrrolidinyl PNA probe: effect of the length and terminating head group of the blocking thiols.
Inhibition of electrochemically controlled bioluminescence of bacterial luciferase by n-alkyl alcohols.
Improved solvent collection system for a dispersive liquid-liquid microextraction of organochlorine pesticides from water using low-density organic solvent.
Synthesis, X-ray crystal structures, thermal and electrochemical properties of thiosemicarbazidatodioxouranium(VI) complexes.
Biotransformation of halogenated nonylphenols with sphingobium xenophagum bayram and a nonylphenol-degrading soil-enrichment culture.
Relation between developmental stage, sensory properties, and volatile content of organically and conventionally grown pac choi (Brassica rapa var. Mei Qing Choi).
Preparation of capsules containing 1-nonanol for rapidly removing high concentration phenol from aqueous solution.
Early calcium increase triggers the formation of olfactory long-term memory in honeybees.
Phase equilibria study of the binary systems (1-butyl-3-methylimidazolium thiocyanate ionic liquid + organic solvent or water).
Production of cyclodextrins in ultrafiltration membrane reactor containing cyclodextrin glycosyltransferase from Bacillus macerans.
Ruthenium-catalyzed C-C bond forming transfer hydrogenation: carbonyl allylation from the alcohol or aldehyde oxidation level employing acyclic 1,3-dienes as surrogates to preformed allyl metal reagents.
Characterization of infrared and near-infrared absorptions of free alcoholic OH groups in hydrocarbon.
Antibacterial activity of long-chain fatty alcohols against Staphylococcus aureus.
Concentration-detection functions for eye irritation evoked by homologous n-alcohols and acetates approaching a cut-off point.
In vitro enzymatic oxidation of a fluorine-tagged sulfido substrate analogue: a 19F NMR investigation.
[Profile-effect on quality control of Houttuynia cordata injection].
Identification of a sex pheromone from male yellow mealworm beetles, Tenebrio molitor.
Molecular restrictions for human eye irritation by chemical vapors.
Olfactory blocking and odorant similarity in the honeybee.
Brownian force profile reconstruction of interfacial 1-nonanol solvent structure.
Comparison of the olfactory sensitivity of two sympatric steppe grasshopper species (Orthoptera: Acrididae) to plant volatile compounds.
Enantiocomplementary enzymatic resolution of the chiral auxiliary: cis,cis-6-(2,2-dimethylpropanamido)spiro[4.4]nonan-1-ol and the molecular basis for the high enantioselectivity of subtilisin Carlsberg.
Biotransformation in double-phase systems: physiological responses of Pseudomonas putida DOT-T1E to a double phase made of aliphatic alcohols and biosynthesis of substituted catechols.
Odor similarity does not influence the time needed for odor processing.
An investigation of chemotaxis in the insect parasitic nematode Heterorhabditis bacteriophora.
Toxic effect of aliphatic alcohols against susceptible and permethrin-resistant Pediculus humanus capitis (Anoplura: Pediculidae).
Solvent effect on ion-pair extraction of 2-(2-pyridylazo)-1-naphthol-4-sulfonate anion with solvated hydroxonium ion using alcohols and 1-octanol/octane mixed solvents.
Detection and quantification of ochratoxin A and deoxynivalenol in barley grains by GC-MS and electronic nose.
A silica-supported, switchable, and recyclable hydroformylation-hydrogenation catalyst.
Straight-chain alcohols exhibit a cutoff in potency for the inhibition of recombinant glutamate receptor subunits.
Development of an attractant for the scarab pest Macrodactylus subspinosus (Coleoptera: Scarabaeidae).
A hairy root culture of melon produces aroma compounds.
A Fluorogenic Reagent, 7-Phenylsulfonyl-4-(2,1,3-benzoxadiazolyl) Isocyanate for Alcohols, with Development Based on the Empirical Method for Prediction.
The effects of selected cotton-leaf volatiles on growth, development and aflatoxin production of Aspergillus parasiticus.
Kinetics and yield of singlet oxygen photosensitized by hypericin in organic and biological media.
Facile Preparation of 3,7-Diazabicyclo[3.3.0]octane and 3,7,10-Triheterocyclic [3.3.3]Propellane Ring Systems from 1,5-Diazacyclooctane 3,7-Derivatives(1).
Qualitative and quantitative analyses of volatiles and pheromone gland extracts collected fromGalleria mellonella (L.) (Lepidoptera: Pyralidae).
Enhancement of propranolol hydrochloride and diazepam skin absorption in vitro. II: Drug, vehicle, and enhancer penetration kinetics.
Effects of several selected odorants on the sodium- and potassium-dependent adenosine triphosphatase activities of two different chicken olfactory tuberinals.
Olfactory sensitivity of two sympatric species of rice leaf folders (Lepidoptera: Pyralidae) to plant volatiles.
Developmental toxicology of industrial alcohols: a summary of 13 alcohols administered by inhalation to rats.
Capillary GLC assay for carbinoxamine and hydrocodone in human serum using nitrogen-sensitive detection.
Specificity of the cis-Isomers of Inhibitors of Uredospore Germination in the Rust Fungi.
The measurement of low concentrations of nonyl alcohol vapour in the air of potato stores during sprout suppression. I. Development of gas chromatographic method and preliminary trial in a commercial store.
THE EFFECT OF TEMPERATURE AND OF LYSIN CONCENTRATION ON THE ACCELERATION OF HEMOLYSIS.

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
FDA Substances Added to Food (formerly EAFUS):View
FDA Indirect Additives used in Food Contact Substances:View
CHEBI:View
CHEMBL:View
Golm Metabolome Database:Search
KEGG (GenomeNet):C14696
HMDB (The Human Metabolome Database):HMDB31265
FooDB:FDB003307
Export Tariff Code:2905.19.0060
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View

PhysChem Properties

Material listed in food chemical codex Yes
Molecular weight 144.25759887695
Specific gravity @ 25 °C
Pounds per Gallon 6.873 to 6.898
Refractive Index 1.431 to 1.435 @ 20 °C
Melting Point -8 to -6°C @ 760 mm Hg
Boiling Point 213 to 215°C @ 760 mm Hg
Acid Value 1 max KOH/g
Vapor Pressure 0.041 mmHg @ 25 °C
Vapor Density 5
Flash Point TCC Value 98 °C TCC
logP (o/w) 3.77
Shelf life 36 months (or longer if stored properly.)
Storage notes Store in cool, dry place in tightly sealed containers, protected from heat and light.
Solubility
alcohol Yes
water, 140 mg/L @ 25 °C (exp) Yes
Stability
non-discoloring in most media Unspecified
shampoo Unspecified

Organoleptic Properties

Odor Type: Floral
fresh, clean, fatty, floral, rose, orange, dusty, wet, oily
Odor strength medium
Substantivity 44 hour(s) at 100.00 %
Luebke, William tgsc, (1982) At 100.00 %. fresh clean fatty floral rose orange dusty wet oily
Flavor Type: Waxy
waxy, citrus, rue, aldehydic, orange, oily, fatty, spicy
Luebke, William tgsc, (1982) Waxy citrus rue aldehydic orange oily fatty spicy
Useful in: brown nuts, fruity citrus, fruity red, fruity others, sweet others. Aldehydic, waxy, citrus, sweet
General comment Oily, fatty, ethereal

Occurrences

Safety Information

Safety information

Preferred SDS: View
European information :
Most important hazard(s):
Xi N - Irritant, Dangerous for the environment.
R 37 - Irritating to respiratory system.
R 51/53 - Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.
S 02 - Keep out of the reach of children.
S 07 - Keep container tightly closed.
S 09 - Keep container in a well-ventilated place.
S 36/37/39 - Wear suitable clothing, gloves and eye/face protection.
S 61 - Avoid release to the environment. Refer to special instructions/safety data sheet.
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
Eye irritation (Category 2A), H319
Acute aquatic toxicity (Category 3), H402
Chronic aquatic toxicity (Category 3), H412
GHS Label elements, including precautionary statements
Pictogramexclamation-mark.jpg
Signal word Warning
Hazard statement(s)
H319 - Causes serious eye irritation
H402 - Harmful to aquatic life
H412 - Harmful to aquatic life with long lasting effects
Precautionary statement(s)
P264 - Wash skin thouroughly after handling.
P273 - Avoid release to the environment.
P280 - Wear protective gloves/protective clothing/eye protection/face protection.
P305 + P351 + P338 - IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P337 + P313 - IF eye irritation persists: Get medical advice/attention.
P501 - Dispose of contents/ container to an approved waste disposal plant.
Human Experience:
2 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50 3560 mg/kg
Food and Cosmetics Toxicology. Vol. 11, Pg. 95, 1973.

intraperitoneal-rat LD50 800 mg/kg
"Patty's Industrial Hygiene and Toxicology," 3rd rev. ed., Clayton, G.D., and F.E. Clayton, eds., New York, John Wiley & Sons, Inc., 1978-82. Vol. 3 originally pub. in 1979; pub. as 2n rev. ed. in 1985.Vol. 2C, Pg. 4628, 1982.

oral-mouse LD50 6400 mg/kg
"Patty's Industrial Hygiene and Toxicology," 3rd rev. ed., Clayton, G.D., and F.E. Clayton, eds., New York, John Wiley & Sons, Inc., 1978-82. Vol. 3 originally pub. in 1979; pub. as 2n rev. ed. in 1985.Vol. 2C, Pg. 4628, 1982.

intraperitoneal-mouse LD50 800 mg/kg
"Patty's Industrial Hygiene and Toxicology," 3rd rev. ed., Clayton, G.D., and F.E. Clayton, eds., New York, John Wiley & Sons, Inc., 1978-82. Vol. 3 originally pub. in 1979; pub. as 2n rev. ed. in 1985.Vol. 2C, Pg. 4628, 1982.

unreported-mammal (species unspecified) LD50 19000 mg/kg
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 51(5), Pg. 61, 1986.

Dermal Toxicity:
skin-rabbit LD50 5660 ul/kg
Food and Cosmetics Toxicology. Vol. 11, Pg. 95, 1973.

Inhalation Toxicity:
inhalation-mouse LC50 5500 mg/m3/2H
"Toxicometric Parameters of Industrial Toxic Chemicals Under Single Exposure," Izmerov, N.F., et al., Moscow, Centre of International Projects, GKNT, 1982Vol. -, Pg. 94, 1982.

inhalation-mammal (species unspecified) LC50 4360 mg/m3
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 51(5), Pg. 61, 1986.

Safety in use information

Category:
flavor and fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for nonanol usage levels up to:
2.0000 % in the fragrance concentrate.
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 3
Click here to view publication 3
average usual ppmaverage maximum ppm
baked goods: -1.90000
beverages(nonalcoholic): -0.70000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: -18.00000
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -0.61000
fruit ices: -0.61000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: -2.00000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: --
sugar substitutes: --
sweet sauces: --

Safety references

European Food Safety Authority (EFSA) reference(s):

Scientific Opinion on the safety and efficacy of straight-chain primary aliphatic alcohols/aldehydes/acids, acetals and esters with esters containing saturated alcohols and acetals containing saturated aldehydes (chemical group 1) when used as flavourings for all animal species
View page or View pdf

EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):143-08-8
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :8914
National Institute of Allergy and Infectious Diseases:Data
WISER:UN 3082
WGK Germany:2
nonan-1-ol
Chemidplus:0000143088
EPA/NOAA CAMEO:hazardous materials
RTECS:RB1575000 for cas# 143-08-8