(Z)-oleyl alcohol
cis-9-octadecenol
 
Notes:
None found
  • BOC Sciences
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      Product(s):
      143-28-2 Oleyl Alcohol technical
       
  • Penta International
    • Penta International Corporation
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      For over 30 years, Penta Manufacturing Company has played a growing role in worldwide chemistry innovations and applications. As an industry leader, Penta continues to pioneer chemistry-based solutions for practically every area of commerce. Our products and expertise have helped fuel technical advances in dozens of commercial applications including flavoring, coloring, fragrances and chemical processes.
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      Product(s):
      15-42500 OLEYL ALCOHOL NF
      15-01550 CIS-9-OCTADECENOL
      15-42505 OLEYL ALCOHOL
       
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    • TCI AMERICA
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      Tokyo Chemical Industry Co., Ltd. (TCI) is a leading worldwide manufacturer of specialty organic chemicals founded in 1946. TCI provides organic laboratory chemicals as well as pharmaceutical, cosmetic and functional materials. More than 70 years of synthesis experience and multi-purpose plants enable TCI to offer more than 30,000 products as well as custom synthesis.
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      Product(s):
      O0058 Oleyl Alcohol >60.0%(GC)
       
Synonyms   Articles   Notes   Search
CAS Number: 143-28-2Picture of molecule3D/inchi
% from: 85.00% to 87.00%
ECHA EINECS - REACH Pre-Reg: 205-597-3
FDA UNII: 172F2WN8DV
Nikkaji Web: J5.818A
Beilstein Number: 1723962
MDL: MFCD00002993
XlogP3: 7.40 (est)
Molecular Weight: 268.48412000
Formula: C18 H36 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Also(can) Contains: hexadecanol 8.00% to 9.00%
 stearyl alcohol 5.00% to 6.00%
Category: cosmetic agents and indirect food additives: paper and paperboard components
 
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
JECFA Food Flavoring: 1637  cis-9-octadecenol
DG SANTE Food Contact Materials: (Z)-oleyl alcohol
FEMA Number: 4363 cis-9-octadecenol
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):143-28-2 ; OLEYL ALCOHOL
FDA Regulation:
FDA PART 176 -- INDIRECT FOOD ADDITIVES: PAPER AND PAPERBOARD COMPONENTS
Subpart B--Substances for Use Only as Components of Paper and Paperboard
Sec. 176.170 Components of paper and paperboard in contact with aqueous and fatty foods.


FDA PART 176 -- INDIRECT FOOD ADDITIVES: PAPER AND PAPERBOARD COMPONENTS
Subpart B--Substances for Use Only as Components of Paper and Paperboard
Sec. 176.180 Components of paper and paperboard in contact with dry food.


FDA PART 176 -- INDIRECT FOOD ADDITIVES: PAPER AND PAPERBOARD COMPONENTS
Subpart B--Substances for Use Only as Components of Paper and Paperboard
Sec. 176.210 Defoaming agents used in the manufacture of paper and paperboard.


FDA PART 177 -- INDIRECT FOOD ADDITIVES: POLYMERS
Subpart B--Substances for Use as Basic Components of Single and Repeated Use Food Contact
Sec. 177.1210 Closures with sealing gaskets for food containers.
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: colorless to pale yellow clear liquid (est)
Assay: 85.00 to 100.00 % sum of isomers
Food Chemicals Codex Listed: No
Specific Gravity: 0.84200 to 0.85400 @  20.00 °C.
Pounds per Gallon - (est).: 7.014 to  7.114
Refractive Index: 1.45000 to 1.46600 @  20.00 °C.
Melting Point: 1.00 to  6.50 °C. @ 760.00 mm Hg
Boiling Point: 207.00 °C. @ 13.00 mm Hg
Boiling Point: 334.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.000010 mmHg @ 25.00 °C. (est)
Flash Point: 338.00 °F. TCC ( 170.00 °C. )
logP (o/w): 7.796 (est)
Soluble in:
 alcohol
 water, 0.02367 mg/L @ 25 °C (est)
Insoluble in:
 water
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Organoleptic Properties:
Odor Description:
at 100.00 %. 
fatty animal
 
Odor and/or flavor descriptions from others (if found).
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: opacifying agents
skin conditioning - emollient
surfactant - emulsifying
viscosity controlling agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
Acme Synthetic Chemicals
Oleyl Alcohol 99% Min
BOC Sciences
For experimental / research use only.
Oleyl Alcohol technical
Carbosynth
For experimental / research use only.
Oleyl alcohol
Croda
Novol™
Odor: bland
Use: Emollient, co-solvent, plasticiser. Outstanding emollient for lipsticks. Also used in creams and lotions, hair conditioners, aqueous/alcoholic systems, hair sprays and other styling products and bath oils.
Diffusions Aromatiques
ALCOOL OLEIQUE
EMD Millipore
For experimental / research use only.
cis-9-Octadecen-1-ol
Jarchem Industries
Jarcol™ 110 BJ
Odor: characteristic
Use: specialty Oleyl/Linoleyl alcohol provides exceptionally high levels of unsaturation (110-135 I.V.) for specialty ethoxylation and esterification reactions. JARCOL 110BJ has significantly higher levels than can be found with standard mono-unsaturated oleyl alcohols.
Jarchem Industries
Jarcol™ 50A
Odor: characteristic
Use: contains substantial amounts of unsaturation (50--55 I.V.) as well as high amounts of saturated alcohol. The most cost effective commericial base alcohol for ethoxylation and esterification reactions.
Jarchem Industries
Jarcol™ 70SP
Odor: characteristic
Use: contains substantial amounts of unsaturation (70-75 I.V.) while still being a very cost effective base alcohol for ethoxylation and esterification reactions.
Jarchem Industries
Jarcol™ 75BJ
Odor: characteristic
Use: contains substantial amounts of unsaturation (70-75 I.V.) while still being a very cost effective base alcohol for ethoxylation and esterification reactions.
Jarchem Industries
Jarcol™ 85BJ
Odor: characteristic
Use: contains higher levels of unsaturation (85-90 I.V.) than is found with traditional oleyl alcohols.
Jarchem Industries
Jarcol™ 90N
Odor: characteristic
Use: contains higher levels of unsaturation (85-95 I.V.) than is found with traditional oleyl alcohols.
Jarchem Industries
Jarcol™ 95BJ
Odor: characteristic
Use: contains the highest level of unsaturation (90-100 I.V.) found in commercially available oleyl alcohols.
Jarchem Industries
Jarcol™ 95CG
Odor: characteristic
Use: Colorless and odorless with excellent thermostability. Used as wetting agent, emulsifier, solubilizer, defoamer and conditioning agent.
Jarchem Industries
Jarcol™ 95P
Odor: characteristic
Use: Meets the criteria set forth by USP standards.
Lipo Chemicals
Lipocol® O/95
Odor: characteristic
Use: Lipocol® O/95 is a natural fatty alcohol that can be used as a coupling agent, plasticizer for hair sprays, emulsion stabilizer and lubricant for aerosols. A liquid fatty alcohol that provides a smooth non oily feel in formulations.
Penta International
CIS-9-OCTADECENOL
Penta International
OLEYL ALCOHOL NF
Penta International
OLEYL ALCOHOL
Santa Cruz Biotechnology
For experimental / research use only.
Oleyl Alcohol
Sarchem Laboratories
For experimental / research use only.
Oleyl Alcohol
Sigma-Aldrich: Aldrich
For experimental / research use only.
Oleyl alcohol, technical grade, 85%
TCI AMERICA
For experimental / research use only.
Oleyl Alcohol >60.0%(GC)
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Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 38 - Irritating to skin.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 36 - Wear suitable protective clothing.
 
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:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: cosmetic agents and indirect food additives: paper and paperboard components
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for (Z)-oleyl alcohol usage levels up to:
  5.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.12 (μg/capita/day)
Modified Theoretical Added Maximum Daily Intake (mTAMDI): 3900 (μg/person/day)
Threshold of Concern:1800 (μg/person/day)
Structure Class: I
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: 23
Click here to view publication 23
 average usual ppmaverage maximum ppm
baked goods: 20.00000100.00000
beverages(nonalcoholic): --
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: --
fruit ices: --
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: --
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: --
 
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
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Safety References:
European Food Safety Athority(EFSA): Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...
EPI System: View
Daily Med: search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 143-28-2
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 5284499
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: nwg
 (Z)-octadec-9-en-1-ol
Chemidplus: 0000143282
RTECS: RG4120000 for cas# 143-28-2
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References:
 (Z)-octadec-9-en-1-ol
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 143-28-2
Pubchem (cid): 5284499
Pubchem (sid): 134973751
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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): D05245
HMDB (The Human Metabolome Database): HMDB29632
Export Tariff Code: 2905.29.9000
FDA Listing of Food Additive Status: View
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Formulations/Preparations:
•oleyl alcohol is sold by henkel under the trade name hd-ocenol. other manufacturers are new japan chemical co., ashland chem. co., and kedzierzyn, poland. •grade: technical, commercial (80-90%) pure. •aldol; atallco o; cachalot o-1; lancol; novol •trade names: aec oleyl alcohol; dermaffine; jeecol o; lipocol o95 protachem oa 7075; sabonal 9095; u-tanol hd 8085; u-tanol hd 9095; u-tanol hd cg •trade name mixtures: base 323 ms; base ral w 323 t; base rouge a levres 323 tal; base rw 101; casto cetyle; castorcet; cloisonne gold cc; cloisonne red cc; fancol iso; flamenco gold cc; flamenco orange cc; flamenco pearl cc; flamenco superpearl cc; flamenco super red cc; flamenco twilight red cc; gemtone sunstone cc; gemtone tan opal cc; ivarbase 3240; liant tw 729; monamilk; oxocap; oxowax; prodhyrouge 2000; ricino - cetyle; unisteron y-50 •adol 80; adol 85; adol 90; cachalot o-3; cachalot o-8; cachalot o-15; crodacol a.10; crodacol o fancol oa 50; fancol oa 70; fancol oa 90; fancol oa 95; hd eutanol; hd oleyl alcohol 7075; hd oleyl alcohol 8085; hd oleyl alcohol 9095; hd oleyl alcohol cg lipocol o-80; lipocol o-9s u-tanol hd; u-tanol hd 7075
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Potential Blenders and core components note
 
For Odor
aldehydic
aldehydic
 dodecanal (aldehyde C-12 lauric)FL/FR
animal
 costus valerolactoneFR
fatty
 allyl octanoateFL/FR
(Z)-dairy lactoneFL/FR
2,4-decadien-1-olFL/FR
(E)-2-decen-1-olFL/FR
(E)-2-decenalFL/FR
 ethyl undecylenateFL/FR
 methyl 10-undecenoateFL/FR
4-methyl octanoic acidFL/FR
(Z)-2-nonenalCS
 octanoic acidFL/FR
(Z)-oleic acidFL/FR
floral
alpha-amyl cinnamaldehyde / methyl anthranilate schiff's baseFR
 decanal / methyl anthranilate schiff's baseFR
fruity
 allyl cyclohexyl propionateFL/FR
 ethyl hexanoateFL/FR
green
 manzanate (Givaudan)FL/FR
soapy
 benzyl laurateFL/FR
 ethyl undecanoateFL/FR
tonka
6-amyl-alpha-pyroneFL/FR
waxy
isoamyl laurateFL/FR
(Z)-5-decen-1-ol 
(E)-2-decen-1-yl acetateFL/FR
1-dodecanolFL/FR
 methyl myristateFL/FR
 methyl undecanoateFR
 myristic acidFL/FR
2,4-nonadien-1-olFL/FR
 palmitic acidFR
 tetradecanalFL/FR
 
For Flavor
 
No flavor group found for these
(Z)-5-decen-1-ol 
(E)-2-decen-1-olFL/FR
(E)-2-decen-1-yl acetateFL/FR
 methyl myristateFL/FR
cooling
 manzanate (Givaudan)FL/FR
creamy
6-amyl-alpha-pyroneFL/FR
ethereal
 benzyl laurateFL/FR
fatty
 allyl octanoateFL/FR
isoamyl laurateFL/FR
(Z)-dairy lactoneFL/FR
2,4-decadien-1-olFL/FR
 ethyl undecylenateFL/FR
4-methyl octanoic acidFL/FR
2,4-nonadien-1-olFL/FR
(E)-2-octenoic acidFL
(Z)-oleic acidFL/FR
 tetradecanalFL/FR
fruity
 allyl cyclohexyl propionateFL/FR
 ethyl (E)-2-octenoateFL
 ethyl hexanoateFL/FR
soapy
 dodecanal (aldehyde C-12 lauric)FL/FR
1-dodecanolFL/FR
 octanoic acidFL/FR
waxy
(E)-2-decenalFL/FR
 ethyl undecanoateFL/FR
 methyl 10-undecenoateFL/FR
 myristic acidFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 emollients 
 emulsifying agents 
 opacifying agents 
 viscosity controlling agents 
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 found in nature
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Synonyms:
 novol
(9Z)-octadec-9-en-1-ol
(Z)-octadec-9-en-1-ol
(Z)-octadec-9-enol
(9Z)-9-octadecen-1-ol
(Z)-9-octadecen-1-ol
cis-octadecen-1-ol
cis-9-octadecen-1-ol
9-octadecen-1-ol, (9Z)-
9-octadecen-1-ol, cis-
(Z)-9-octadecenol
cis-9-octadecenol
cis-9-octadecenyl alcohol
 oleyl alcohol NF
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: Permeability of acetic acid through organic films at the air-aqueous interface.
PubMed: Dialkyl 3,3'-thiodipropionate and dialkyl 2,2'-thiodiacetate antioxidants by lipase-catalyzed esterification and transesterification.
PubMed: Natural ligands of hamster aphrodisin.
PubMed: Lipase specificity toward some acetylenic and olefinic alcohols in the esterification of pentanoic and stearic acids.
PubMed: Evidence that His110 of the protein FadL in the outer membrane of Escherichia coli is involved in the binding and uptake of long-chain fatty acids: possible role of this residue in carboxylate binding.
PubMed: A novel CoA-independent transacetylase produces the ethanolamine plasmalogen and acyl analogs of platelet-activating factor (PAF) with PAF as the acetate donor in HL-60 cells.
PubMed: Metabolism of long-chain alcohols in cell suspension cultures of soya and rape.
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