cetyl lactate
hexadecyl lactate
 
Notes:
None found
  • BOC Sciences
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      Product(s):
      35274-05-6 Cetyl Lactate
       
  • Penta International
    • Penta International Corporation
      Chemistry innovation
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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):
      03-18240 CETYL LACTATE
       
  • TCI AMERICA
    • TCI AMERICA
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      Product(s):
      H1159 Hexadecyl Lactate
       
Synonyms   Articles   Notes   Search
CAS Number: 35274-05-6Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 252-478-7
FDA UNII: A7EVH2RK4O
Nikkaji Web: J260.566J
MDL: MFCD00152336
XlogP3-AA: 7.60 (est)
Molecular Weight: 314.50946000
Formula: C19 H38 O3
NMR Predictor: Predict (works with chrome or firefox)
Category: solvents/deluents for flavor and/or 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
PubMed: Search
NCBI: Search
JECFA Food Flavoring: 1950  hexadecyl lactate
FEMA Number: 4483 hexadecyl lactate
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):35274-05-6 ; HEXADECYL LACTATE
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Physical Properties:
Appearance: white solid (est)
Assay: 88.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 0.89300 to 0.90500 @  28.00 °C.
Pounds per Gallon - (est).: 7.431 to  7.531
Melting Point: 41.00 °C. @ 760.00 mm Hg
Boiling Point: 353.00 to  354.00 °C. @ 760.00 mm Hg
Acid Value: 3.00 max. KOH/g
Saponification Value: 174.00 to 189.00
Vapor Pressure: 0.000001 mmHg @ 25.00 °C. (est)
Flash Point: 320.00 °F. TCC ( 160.00 °C. )
logP (o/w): 7.094 (est)
Soluble in:
 alcohol
 water, 0.0629 mg/L @ 25 °C (est)
Similar Items: note
amyl lactate
isoamyl lactate
benzyl lactate
butyl butyryl lactate
butyl lactate
isobutyl lactate
sec-butyl lactate
butyl laevo-lactate
dodecyl lactate
ethyl acetyl lactate
ethyl butyryl lactate
ethyl lactate
ethyl phenyl lactate
(Z)-3-hexen-1-yl lactate
hexyl lactate
laevo-menthyl lactate
menthyl methyl lactate
methyl dextro-lactate
methyl laevo-lactate
phenethyl lactate
propyl lactate
vanillyl lactate
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Organoleptic Properties:
 
Odor Type: buttery
 
Odor Strength: low
 
 fatty  buttery  
Odor Description:
at 100.00 %. 
faint fatty buttery
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: skin conditioning
skin conditioning - emollient
Synonyms   Articles   Notes   Search   Top
Suppliers:
Alzo International
Dermol CL
Alzo International
Wickenol 507
Axsyn
For experimental / research use only.
Propanoic acid,2-hydroxy-, hexadecyl ester
BOC Sciences
For experimental / research use only.
Cetyl Lactate
Inoue Perfumery
HEXADECYL LACTATE
Penta International
CETYL LACTATE
Santa Cruz Biotechnology
For experimental / research use only.
Hexadecyl Lactate
Sigma-Aldrich: Aldrich
For experimental / research use only.
Hexadecyl Lactate
TCI AMERICA
For experimental / research use only.
Hexadecyl Lactate
Universal Preserv-A-Chem Inc.
Cetyl Lactate
Odor: characteristic
Use: Used in lipsticks, mascaras, nail polish removers, hand lotions, cream, rouges and many other cosmetics, shampoos, hair lacquers and other hair products, deodorants, antiperspirants.
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Safety Information:
Preferred SDS: View
 
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
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Safety in Use Information:
Category: solvents/deluents for flavor and/or fragrance agents
Recommendation for cetyl lactate usage levels up to:
 not for fragrance use.
 
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: 24
Click here to view publication 24
 average usual ppmaverage maximum ppm
baked goods: 2.0000050.00000
beverages(nonalcoholic): 0.100001.00000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: 20.00000250.00000
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: 2.0000050.00000
fish products: --
frozen dairy: 0.200002.00000
fruit ices: 0.200002.00000
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: --
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 35274-05-6
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 37098
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 hexadecyl 2-hydroxypropanoate
Chemidplus: 0035274056
Synonyms   Articles   Notes   Search   Top
References:
 hexadecyl 2-hydroxypropanoate
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 35274-05-6
Pubchem (cid): 37098
Pubchem (sid): 134998464
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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
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2918.11.5100
ChemSpider: View
FAO: Hexadecyl lactate
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
 emollients 
 skin conditioning 
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
 ceraphyl 28
 dermol CL
1-hexadecanol lactate
 hexadecyl 2-hydroxypropanoate
 hexadecyl lactate
N-hexadecyl lactate
 hexadecyl-2-hydroxypropanoate
N-hexadecyl-2-hydroxypropanoate
2-hydroxypropanoic acid hexadecyl ester
2-hydroxypropionic acid hexadecyl ester
 lactic acid cetyl ester
 lactic acid hexadecyl ester
 propanoic acid, 2-hydroxy-, hexadecyl ester
 propanoic acid,2-hydroxy-, hexadecyl ester
 wickenol 507
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: Dipalmitoyl-phosphatidylcholine biosynthesis is induced by non-injurious mechanical stretch in a model of alveolar type II cells.
PubMed: Charged polylactide co-glycolide microparticles as antigen delivery systems.
PubMed: Straightforward synthesis of two pairs of enantiomeric butenolides 3-tetradecyl- and 3-hexadecyl-5-methyl-2(5H)-furanone.
PubMed: Effects of Actinomyces amphiphile on the fluidity of endothelial cells: a spin label study.
PubMed: A comparison of the lytic properties of two ether-linked lipids, one with and one without antineoplastic activity.
PubMed: A phospholipase A2 inhibitor decreases generation of thiobarbituric acid reactive substance during lung ischemia-reperfusion.
PubMed: Selective suppression of lipid resonances by lipid-soluble nitroxides in NMR spectroscopy.
PubMed: Mechanisms for cardiac depression induced by phorbol myristate acetate in working rat hearts.
PubMed: Enhancing effect of cetyl lactate on the percutaneous absorption of indomethacin in rats.
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