Substance

ID:718030

Names and Identifiers
IUPAC name
cyclohexanamine
IUPAC Traditional name
cyclohexylamine
Synonyms
Aminocyclohexane环己胺Cyclohexylamine
Registration numbers
EC Number
CAS Number
Beilstein Number
MDL Number
Merck Index
Properties
Product Information
Purity
98+%
Safety Information
European Hazard Symbols
Corrosive Corrosive (C)
Harmful Harmful (X)
GHS Pictograms
GHS05
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
GHS08
Respiratory sensitization, category 1
Germ cell mutagenicity, categories 1A,1B,2
Carcinogenicity, categories 1A,1B,2
Reproductive toxicity, categories 1A,1B,2
Specific Target Organ Toxicity – Single exposure, categories 1,2
Specific Target Organ Toxicity – Repeated exposure, categories 1,2
Aspiration Hazard, category 1
GHS02
Flammable gases, category 1
Flammable aerosols, categories 1,2
Flammable liquids, categories 1,2,3
Self-reactive substances and mixtures, Types B,C,D,E,F
Pyrophoric liquids, category 1
Pyrophoric solids, category 1
Self-heating substances and mixtures
Substances and mixtures, which in contact with water, emit flammable gases, categories 1,2,3
Organic peroxides, Types B,C,D,E,F
GHS07
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Hazard Class
8
Packing Group
II
GHS Hazard statements
H314-H226-H361-H302-H312
Risk Statements
10-21/22-34-62
Safety Statements
1/2-26-36/37/39-45
RTECS
GX0700000
GHS Precautionary statements
P210-P241-P303+P361+P353-P305+P351+P338-P405-P501A
Storage Warning
Air Sensitive
TSCA Listed
UN Number
UN2357
Physical Property
Density
0.868
Melting Point
-18°C
Refractive Index
1.4585
Boiling Point
133-134°C
Flash Point
27°C(81°F)
Molecule Details
No Data Available
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Molecular Spectra
No Data Available
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References
• For protection of an aldehyde as its cyclohexyl imine, see, e.g.: Org. Synth. Coll., 8, 586 (1993). Cyclohexyl imines of aldehydes have found use in the directed aldol synthesis: reaction with a less reactive ketone takes place in preference to self-condensation of the aldehyde. See, e.g.: Org. Synth. Coll., 6, 901 (1988):