BETA-CYCLOCITRAL

BETA-CYCLOCITRAL
  • CAS No.:432-25-7
Other grades of this product :
BETA-CYCLOCITRAL Basic information
Product Name:BETA-CYCLOCITRAL
Synonyms:Pentadeuterio--cyclocitral;^b-Cyclocitral, 90+%;1-Cyclohexene-1-carboxaldehyde, 2,6,6-trimethyl-;1-Formyl-2,6,6-trimethyl-1-cyclohexene;2,6,6-Trimethyl-1-cyclohexene-1-carbaldehyde;-Cyclocitral, Technical Grade;β-Cyclocitral,2,6,6-Trimethyl-1-cyclohexene-1-carboxaldehyde;beta-Cyclocitral (tech grade)
CAS:432-25-7
MF:C10H16O
MW:152.23
EINECS:207-081-3
Product Categories:Chiral Reagents
Mol File:432-25-7.mol
BETA-CYCLOCITRAL Chemical Properties
Melting point 62-63 C
Boiling point 62-63 °C3 mm Hg(lit.)
density 0.943 g/mL at 25 °C(lit.)
refractive index n20/D 1.497(lit.)
FEMA 3639 | 2,6,6-TRIMETHYL-1&2-CYCLOHEXEN-1-CARBOXALDEHYDE
Fp >230 °F
storage temp. Inert atmosphere,Store in freezer, under -20°C
solubility Chloroform (Slightly), Dichloromethane, Ethyl Acetate (Slightly), Methanol (Slig
form Oil
color Colourless to Dark Yellow
Water Solubility Soluble in chloroform, dichloromethane, ethyl acetate and methanol. Insoluble in water.
Sensitive Air Sensitive
JECFA Number979
Stability:Light Sensitive
EPA Substance Registry System1-Cyclohexene-1-carboxaldehyde, 2,6,6-trimethyl- (432-25-7)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 20/21/22-36/37/38
Safety Statements 26-36-37/39
RIDADR 1760
WGK Germany 3
TSCA Yes
HazardClass 8
PackingGroup III
HS Code 29122990
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
BETA-CYCLOCITRAL Usage And Synthesis
Chemical PropertiesColourless Oil
Chemical Properties2,6,6-Trimethyl-1,2-cyclohexen-1-carboxaldehyde has a camphoraceous odor for a 50/50 mixture of isomers.
OccurrenceReported found in tea, apricot, melon, tomato, tomato paste, ginger, rum, Japanese plum, plumcot, mango, apple brandy, calamus, buckwheat, Bourbon vanilla, cape gooseberry and maté.
Usesbeta-Cyclocitral is used as flavoring agent, nutrient, stabilizers, surfactants and emulsifiers.
DefinitionChEBI: A monoterpenoid formally derived from citral by cyclisation. It is a volatile compound produced by a cyanobacteria.
Synthesis Reference(s)Journal of the American Chemical Society, 69, p. 2072, 1947 DOI: 10.1021/ja01200a519Synthesis, p. 781, 1975

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