cyclohexane carboxaldehyde
cyclohexylformaldehyde
 
Notes:
None found
  • BOC Sciences
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      Product(s):
      2043-61-0 CYCLOHEXANECARBALDEHYDE 95%
       
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      Product(s):
      C0880 Cyclohexanecarboxaldehyde >98.0%(GC)
       
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CAS Number: 2043-61-0Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 218-057-7
FDA UNII: SW0X317TE3
Nikkaji Web: J7.861A
Beilstein Number: 878306
MDL: MFCD00001457
XlogP3-AA: 1.80 (est)
Molecular Weight: 112.17184000
Formula: C7 H12 O
NMR Predictor: Predict (works with chrome or firefox)
Category: information only not used for fragrances or flavors
 
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
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 0.92700 to 0.93200 @  20.00 °C.
Pounds per Gallon - (est).: 7.723 to  7.764
Refractive Index: 1.44900 to 1.45200 @  20.00 °C.
Boiling Point: 159.30 °C. @ 760.00 mm Hg
Vapor Pressure: 2.500000 mmHg @ 25.00 °C. (est)
Flash Point: 105.00 °F. TCC ( 40.56 °C. )
logP (o/w): 1.900 (est)
Soluble in:
 water, 1709 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
BOC Sciences
For experimental / research use only.
CYCLOHEXANECARBALDEHYDE 95%
Santa Cruz Biotechnology
For experimental / research use only.
Cyclohexanecarboxaldehyde 97%
Sigma-Aldrich: Aldrich
For experimental / research use only.
Cyclohexanecarboxaldehyde 97%
TCI AMERICA
For experimental / research use only.
Cyclohexanecarboxaldehyde >98.0%(GC)
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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: information only not used for fragrances or flavors
Recommendation for cyclohexane carboxaldehyde usage levels up to:
 not for fragrance use.
 
Recommendation for cyclohexane carboxaldehyde flavor usage levels up to:
 not for flavor use.
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Safety References:
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 : 16275
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 cyclohexanecarbaldehyde
Chemidplus: 0002043610
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References:
 cyclohexanecarbaldehyde
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 16275
Pubchem (sid): 134982508
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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
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2912.29.6000
ChemSpider: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
 cyclohexane formaldehyde
 cyclohexanealdehyde
 cyclohexanecarbaldehyde
 cyclohexanecarboxaldehyde
 cyclohexanecarboxaldehyde (8CI)(9CI)
 cyclohexyl carboxaldehyde
 cyclohexyl formaldehyde
 cyclohexylformaldehyde
1-formyl cyclohexane
 formylcyclohexane
1-formylcyclohexane
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Articles:
PubMed: Nucleophilic reactivity of a series of peroxomanganese(III) complexes supported by tetradentate aminopyridyl ligands.
PubMed: P(PhCH(2)NCH(2)CH(2))(3)N: an efficient lewis base catalyst for the synthesis of propargylic alcohols and Morita-Baylis-Hillman adducts via aldehyde alkynylation.
PubMed: N-heterocyclic carbene-catalyzed silyl enol ether formation.
PubMed: 3-bromozinc propenyl esters: an experimental and theoretical study of the unique stereocrossover observed in their addition to aromatic and aliphatic aldehydes.
PubMed: Structure-function analysis of the vanillin molecule and its antifungal properties.
PubMed: Ciclesonide: a novel inhaled corticosteroid for asthma.
PubMed: Catalytic, highly enantio- and diastereoselective pinacol coupling reaction with a new tethered bis(8-quinolinolato) ligand.
PubMed: Cinchona alkaloid-lewis acid catalyst systems for enantioselective ketene-aldehyde cycloadditions.
PubMed: Modular ligands derived from amino acids for the enantioselective addition of organozinc reagents to aldehydes.
PubMed: Preparation of Chiral Allenylmetal Reagents from Enantioenriched Allenyl Iodides and Propargylic Mesylates. A Comparison of Indium, Bismuth, and Tin Derivatives.
PubMed: Metal- and Ligand-Accelerated Catalysis of the Baylis-Hillman Reaction.
PubMed: EPR spectrometry of cytochrome P450 2B4: effects of mutations and substrate binding.
PubMed: Enantiospecific Formation of Trans 1,3-Disubstituted Tetrahydro-beta-carbolines by the Pictet-Spengler Reaction and Conversion of Cis Diastereomers into Their Trans Counterparts by Scission of the C-1/N-2 Bond.
PubMed: Synthesis of Chiral alpha,delta-Dioxygenated Allylic Stannanes as Reagents for Carbohydrate Synthesis and Homologation.
PubMed: The aromatization of cyclohexanecarboxylic acid to hippuric acid: substrate specificity and species differences.
PubMed: Sensory irritation response to inhaled aldehydes after formaldehyde pretreatment.
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