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alpha-amyl cinnamylidene / methyl anthranilate schiff's base
alpha-pentylcinnamylidene / methyl anthranilate schiff's base

Supplier Sponsors

Name:methyl 2-[[(2E)-2-benzylideneheptylidene]amino]benzoate
CAS Number: 68527-78-6Picture of molecule3D/inchi
Other(deleted CASRN):73791-24-9
ECHA EINECS - REACH Pre-Reg:271-283-8
FDA UNII: Search
Nikkaji Web:J60.366J
XlogP3-AA:5.90 (est)
Molecular Weight:335.44665000
Formula:C22 H25 N O2
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
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PubMed:Search
NCBI:Search
 
Physical Properties:
Food Chemicals Codex Listed: No
Boiling Point: 486.00 to 487.00 °C. @ 760.00 mm Hg (est)
Flash Point: 363.00 °F. TCC ( 184.10 °C. ) (est)
logP (o/w): 6.583 (est)
Soluble in:
 water, 0.03063 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: perfuming agents
 
Suppliers:
BOC Sciences
For experimental / research use only.
a-Amylcinnamaldehyde-methyl anthranilate
 
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:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
IFRA Critical Effect:
Dermal sensitization and systemic toxicity
IFRA fragrance material specification:
 The IFRA Scientific Committee examined the physicochemical properties of Schiff bases and concluded that, based on the available information, these materials should be considered under contributions from other sources. By default, the stoichiometric presence of the aldehydes of the Schiff bases is taken into account assuming 100% dissociation. An indicative list of Schiff bases incorporating aldehydes covered by an IFRA Standard of restriction is reported at page 2. These Schiff bases must be taken into account for determination of the maximum use level of the respective aldehydes.
contains the following IFRA (Annex) restricted components: (non-analysis max. level reference only)
á-Amylcinnamaldehyde Max. Found: 60.30 % and Reason: Sensitization
 View the IFRA Standard
 
Recommendation for alpha-amyl cinnamylidene / methyl anthranilate schiff's base flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):68527-78-6
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :6435059
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:2
methyl 2-[[(2E)-2-benzylideneheptylidene]amino]benzoate
Chemidplus:0068527786
 
References:
 methyl 2-[[(2E)-2-benzylideneheptylidene]amino]benzoate
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:68527-78-6
Pubchem (cid):6435059
Pubchem (sid):135010207
 
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):Search
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
alpha-amyl cinnamylidene methyl anthranilate schiff's base
alpha-amylcinnamylidene / methyl anthranilate schiff's base
 anthranilic acid, N-(2-benzylideneheptylidene)-, methyl ester
 benzoic acid, 2-((2-(phenylmethylene)heptylidene)amino)-, methyl ester
 benzoic acid, 2-[[2- (phenylmethylene)heptylidene]amino]-, methyl ester
 benzoic acid, 2-[[2-(phenylmethylene)heptylidene]amino]-, methyl ester
 methyl 2-((2-(phenyl methylene)heptylidene)amino) benzoate
 methyl 2-[(2-benzylideneheptylidene)amino]benzoate
 methyl 2-[[(2E)-2-benzylideneheptylidene]amino]benzoate
 methyl 2-{[2-(phenylmethylene)heptylidene]amino}benzoate
 methyl 2-cinnamylidene anthranilate
alpha-methyl anthranilate / amyl cinnamylidene schiff's base
 methyl N-(2-amyl-3-phenyl propenylidene) anthranilate
 methyl N-(2-amyl-3-phenylpropenylidene)anthranilate
 methyl N-(b-pentylcinnamylidene)anthranilate
alpha-pentyl cinnamylidene / methyl anthranilate schiff's base
alpha-pentylcinnamylidene / methyl anthranilate schiff's base
 
 
Notes:
None found
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