Product Name

  • Name

    1-Cyclohexylethanol

  • EINECS 214-780-7
  • CAS No. 1193-81-3
  • Article Data202
  • CAS DataBase
  • Density 0.928 g/mL at 25 °C(lit.)
  • Solubility 5.163g/L at 24℃
  • Melting Point 140 °C
  • Formula C8H16O
  • Boiling Point 189 °C(lit.)
  • Molecular Weight 128.214
  • Flash Point 163 °F
  • Transport Information
  • Appearance
  • Safety 23-24/25
  • Risk Codes 36/37/38
  • Molecular Structure Molecular Structure of 1193-81-3 (1-Cyclohexylethanol)
  • Hazard Symbols
  • Synonyms (1-Hydroxyethyl)cyclohexane;1-Cyclohexane-1-ethanol;1-Cyclohexyl-1-ethanol;Cyclohexylmethylcarbinol;Ethanol, 1-cyclohexyl-;Methanol, cyclohexylmethyl-;Methylcyclohexylcarbinol;Methylcyclohexylmethanol;NSC 44898;NSC 9476;Surflot 944;a-Methylcyclohexanemethanol;
  • PSA 20.23000
  • LogP 1.94750

Synthetic route

acetophenone
98-86-2

acetophenone

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Conditions
ConditionsYield
With hydrogen In water at 100℃; under 15001.5 Torr; for 0.333333h;100%
With ruthenium nanoparticles at 120℃; under 90009 Torr; for 2h; Ionic liquid; Autoclave;99%
With ruthenium; hydrogen In water at 30℃; under 22801.5 Torr; for 12h; Autoclave;94%
Cyclohexyl methyl ketone
823-76-7

Cyclohexyl methyl ketone

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Conditions
ConditionsYield
Stage #1: Cyclohexyl methyl ketone With formic acid; tricarbonyl (4S,7S)-4,7-bis(benzyloxy)-1,3-diphenyl-4,5,6,7-tetrahydro-2H-inden-2-one iron; triethylamine for 0.166667h; Inert atmosphere;
Stage #2: With trimethylamine-N-oxide at 60℃; for 48h; Reagent/catalyst; Concentration; Temperature;
97%
With sodium isopropylate; isopropyl alcohol; ruthenium complex C38H42N2O4P2Ru for 5h; Catalytic hydrogenation; Catalytic transfer hydrogenation;91%
With methanol; sodium tetrahydroborate at 0 - 20℃; for 0.666667h; Inert atmosphere;88%
tert-Butyl-(1-cyclohexyl-ethoxy)-dimethyl-silane

tert-Butyl-(1-cyclohexyl-ethoxy)-dimethyl-silane

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Conditions
ConditionsYield
With water; scandium tris(trifluoromethanesulfonate) In acetonitrile for 4h; Ambient temperature;97%
methyltrichlorotitanium
2747-38-8

methyltrichlorotitanium

cyclohexanone
108-94-1

cyclohexanone

A

1-Methylcyclohexanol
590-67-0

1-Methylcyclohexanol

B

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Conditions
ConditionsYield
With Methyltitantrichlorid,Triphenylphosphin; cyclohexanecarbaldehyde In dichloromethane at -25℃; for 6h; Product distribution; other phosphane-complexes and reagents;A 95%
B 3%
cyclohexanone
108-94-1

cyclohexanone

MeTiCl3

MeTiCl3

A

1-Methylcyclohexanol
590-67-0

1-Methylcyclohexanol

B

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Conditions
ConditionsYield
With Methyltitantrichlorid,Triphenylphosphin; cyclohexanecarbaldehyde In dichloromethane at 0℃; for 6h;A 95%
B 3%
2-methyl-1-oxaspiro[2.5]octane
17328-74-4

2-methyl-1-oxaspiro[2.5]octane

A

1-ethylcyclohexanol
1940-18-7

1-ethylcyclohexanol

B

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

C

1-(1-chlorocyclohexyl)ethanol

1-(1-chlorocyclohexyl)ethanol

Conditions
ConditionsYield
With bis(cyclopentadienyl)titanium (III) chloride; cyclohexa-1,4-diene In tetrahydrofuran Product distribution; Mechanism; Ambient temperature; other epoxides, reaction without cyclohexa-1,4-diene;A 1.5%
B 92%
C 0.9%
With bis(cyclopentadienyl)titanium (III) chloride; cyclohexa-1,4-diene In tetrahydrofuran Ambient temperature;A 1.5%
B 92%
C 0.9%
With bis(cyclopentadienyl)titanium (III) chloride; cyclohexa-1,4-diene In tetrahydrofuran for 0.666667h; Product distribution; Mechanism; other epoxides; other H-atom donors; var. temperature, var. time;A 1.5%
B 64%
C 0.9%
With bis(cyclopentadienyl)titanium (III) chloride; cyclohexa-1,4-diene In tetrahydrofuran for 0.25h;A n/a
B 64%
C 0.9%
With bis(cyclopentadienyl)titanium (III) chloride; cyclohexa-1,4-diene In tetrahydrofuran for 0.25h; Yields of byproduct given;A n/a
B n/a
C 0.9%
2-(2,6-dimethoxyphenoxy)-1-phenylethan-1-ol
145804-82-6

2-(2,6-dimethoxyphenoxy)-1-phenylethan-1-ol

A

1,3-dimethoxy-2-hydroxy-benzene
91-10-1

1,3-dimethoxy-2-hydroxy-benzene

B

ethylbenzene
100-41-4

ethylbenzene

C

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Conditions
ConditionsYield
With Ni0.85Ru0.15; hydrogen In water at 95℃; under 760.051 Torr; for 16h; Reagent/catalyst;A 92%
B 58%
C 22%
(1-cyclohexylethoxy)trimethylsilane

(1-cyclohexylethoxy)trimethylsilane

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Conditions
ConditionsYield
With water; boric acid at 20℃; for 1h;90%
methyltrichlorotitanium
2747-38-8

methyltrichlorotitanium

cyclohexanecarbaldehyde
2043-61-0

cyclohexanecarbaldehyde

A

n-hexan-2-one
591-78-6

n-hexan-2-one

B

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Conditions
ConditionsYield
With n-hexan-2-one; Methyltitantrichlorid,Triphenylphosphin In dichloromethane at -25℃; for 6h; Product distribution; other phosphane-complexes and reagents;A 6%
B 89%
cyclohexanecarbaldehyde
2043-61-0

cyclohexanecarbaldehyde

MeTiCl3

MeTiCl3

A

1-Methylcyclohexanol
590-67-0

1-Methylcyclohexanol

B

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Conditions
ConditionsYield
With n-hexan-2-one; Methyltitantrichlorid,Triphenylphosphin In dichloromethane at -25℃; for 6h;A 6%
B 89%
2-methyl-4,7-dihydro-1,3-dioxepine
7045-86-5

2-methyl-4,7-dihydro-1,3-dioxepine

cyclohexylmagnesium bromide
931-50-0

cyclohexylmagnesium bromide

A

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

B

(2Z)-4-cyclohexyl-1-hydroxy-2-butene
119624-68-9

(2Z)-4-cyclohexyl-1-hydroxy-2-butene

Conditions
ConditionsYield
1,2-bis(diphenylphosphino)ethane nickel(II) chloride for 8h; Ambient temperature; Yields of byproduct given;A n/a
B 88%
methyltriisopropoxytitanium(IV)
18006-13-8

methyltriisopropoxytitanium(IV)

cyclohexanecarbaldehyde
2043-61-0

cyclohexanecarbaldehyde

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Conditions
ConditionsYield
In diethyl ether at 0℃; for 0.5h;85%
In dichloromethane at 22℃; for 0.5h;95 % Spectr.
2-methyl-1-oxaspiro[2.5]octane
17328-74-4

2-methyl-1-oxaspiro[2.5]octane

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Conditions
ConditionsYield
With manganese; cyclohexa-1,4-diene; titanocene dichloride; 2,4,6-collidine hydrochloride In tetrahydrofuran for 16h;81%
With bis(cyclopentadienyl)titanium dichloride; collidine hydrochloride; cyclohexa-1,4-diene; zinc In tetrahydrofuran for 30h; Ambient temperature;76%
dimethyldichlorotitanium(IV)
35739-70-9

dimethyldichlorotitanium(IV)

cyclohexanecarbaldehyde
2043-61-0

cyclohexanecarbaldehyde

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Conditions
ConditionsYield
In dichloromethane at -40℃; for 1h;78%
trimethylaluminum
75-24-1

trimethylaluminum

cyclohexanecarbaldehyde
2043-61-0

cyclohexanecarbaldehyde

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Conditions
ConditionsYield
With bis(acetylacetonate)nickel(II); triphenylphosphine In tetrahydrofuran; hexane at 0℃; for 11h;76%
With 2,7-dimethyl-1,8-biphenylenediol 1.) CH2Cl2, hexane, r.t., 30 min, 2.) CH2Cl2, hexane, -78 deg C, 1 h; Yield given. Multistep reaction;

A

B

C

D

A

B

C

A

B

rac-1-cyclohexylethanol

rac-1-cyclohexylethanol

C

Diphenyl-methanone O-(1-cyclohexyl-ethyl)-oxime

Diphenyl-methanone O-(1-cyclohexyl-ethyl)-oxime

Conditions
ConditionsYield
In diethyl ether; toluene Heating; Yields of byproduct given;A n/a
B 75%
C n/a
dimethyl zinc(II)
544-97-8

dimethyl zinc(II)

buta-1,3-diene
106-99-0

buta-1,3-diene

cyclohexanecarbaldehyde
2043-61-0

cyclohexanecarbaldehyde

A

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

B

(E)-1-Cyclohexyl-hex-3-en-1-ol

(E)-1-Cyclohexyl-hex-3-en-1-ol

C

(3E,7E)-1-Cyclohexyl-deca-3,7-dien-1-ol

(3E,7E)-1-Cyclohexyl-deca-3,7-dien-1-ol

Conditions
ConditionsYield
bis(acetylacetonate)nickel(II) In tetrahydrofuran; hexane at 25℃; for 1h; Addition;A 10%
B 73%
C 17%
acetophenone
98-86-2

acetophenone

A

ethyl-cyclohexane
1678-91-7

ethyl-cyclohexane

B

ethylbenzene
100-41-4

ethylbenzene

C

1-Phenylethanol
98-85-1, 13323-81-4

1-Phenylethanol

D

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Conditions
ConditionsYield
With hydrogen; Pd APII Deloxan at 200℃; under 90007.2 Torr;A n/a
B 69%
C n/a
D n/a
With hydrogen; Pd APII Deloxan In various solvent(s) at 90℃; under 90007.2 Torr; Product distribution; various temp. and pressures;
With carbon dioxide; hydrogen at 180℃; under 90009 Torr; Supercritical conditions; Flow reactor;A 17 %Spectr.
B 41 %Spectr.
C 14 %Spectr.
D 28 %Spectr.
2-phenoxy-1-phenylethanone
721-04-0

2-phenoxy-1-phenylethanone

A

1-Phenylethanol
98-85-1, 13323-81-4

1-Phenylethanol

B

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

C

cyclohexanol
108-93-0

cyclohexanol

D

phenol
108-95-2

phenol

Conditions
ConditionsYield
With isopropyl alcohol In aq. buffer at 60℃; for 9h; pH=8; Electrochemical reaction;A 9%
B 63%
C 69%
D 28%
rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

acetic anhydride
108-24-7

acetic anhydride

1-cyclohexylethan-1-yl acetate
13487-27-9

1-cyclohexylethan-1-yl acetate

Conditions
ConditionsYield
With dmap In ethyl acetate100%
With copper(II) bis(trifluoromethanesulfonate) In dichloromethane for 0.5h; Ambient temperature;96%
With copper(II) bis(trifluoromethanesulfonate) In dichloromethane at 20℃; for 1h;96%
oxalyl dichloride
79-37-8

oxalyl dichloride

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

2-(1-cyclohexylethoxy)-2-oxoacetic acid

2-(1-cyclohexylethoxy)-2-oxoacetic acid

Conditions
ConditionsYield
In diethyl ether at 0 - 20℃;100%
rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Cyclohexyl methyl ketone
823-76-7

Cyclohexyl methyl ketone

Conditions
ConditionsYield
With aluminum oxyhydroxide; ruthenium In toluene at 110℃; for 12h;99%
With nickel(II) triflate; cyclohexanone; 1,2-bis-(dicyclohexylphosphino)ethane In toluene at 110℃; for 12h; Schlenk technique;99%
[(η5-(4-HOCH2C6H4)Ph3C4CO)2H]Ru2((CO)4)(μ-H)-SiO2 In toluene at 110℃; for 8h;97%
rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Diethyl carbonate
105-58-8

Diethyl carbonate

ethyl 1-cyclohexylethyl carbonate

ethyl 1-cyclohexylethyl carbonate

Conditions
ConditionsYield
aluminum oxide; cesium fluoride at 129.85℃; for 0.75h;98%
With immobilized 1,5,7-triazabicyclo[4.4.0]dec-5-ene on magnetic γ-Fe2O3 nanoparticles at 125℃; for 6h;96%
rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

1,1,1,3,3,3-hexamethyl-disilazane
999-97-3

1,1,1,3,3,3-hexamethyl-disilazane

(1-cyclohexylethoxy)trimethylsilane

(1-cyclohexylethoxy)trimethylsilane

Conditions
ConditionsYield
N,N'-dibromo-N,N'-1,2-ethanediylbis-(benzenesulfonamide) at 20℃; for 7.5h;96%
Stage #1: rac-1-cyclohexylethanol With Iron(III) nitrate nonahydrate; sodium iodide In dichloromethane at 20℃;
Stage #2: 1,1,1,3,3,3-hexamethyl-disilazane In dichloromethane at 20℃;
95%
With boric acid In acetonitrile at 20℃; for 1.1h;95%
rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

ethyl carbonate derivative

ethyl carbonate derivative

ethyl 1-cyclohexylethyl carbonate

ethyl 1-cyclohexylethyl carbonate

Conditions
ConditionsYield
With γ-Fe2O3-immobilized 1,5,7-triazabicyclo[4.4.0]dec-5-ene nanoparticles (MNPs-TBD) at 125℃; for 6h;96%
rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

C8H15O4S(1-)*Na(1+)

C8H15O4S(1-)*Na(1+)

Conditions
ConditionsYield
Stage #1: rac-1-cyclohexylethanol With sodium hydride In 1,4-dioxane at 20℃; for 1h;
Stage #2: With triethylamine sulfurtrioxide In 1,4-dioxane at 20℃;
95%
rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

C36H24F6O5

C36H24F6O5

1-Cyclohexylethyl α-<1-(9-anthryl)-2,2,2-trifluoroethoxy>acetate
77507-28-9

1-Cyclohexylethyl α-<1-(9-anthryl)-2,2,2-trifluoroethoxy>acetate

Conditions
ConditionsYield
With pyridine In tetrahydrofuran94%
4-chlorophenyl acetate
876-27-7

4-chlorophenyl acetate

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

(R)-1-cyclohexylethyl acetate
58396-29-5

(R)-1-cyclohexylethyl acetate

Conditions
ConditionsYield
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; Candida antarctica B lipase; [RuCl2(p-cymene)]2; (E)-2-((1-hydroxy-2-methylpropan-2-ylimino)methyl)phenol In toluene at 70℃; for 72h; Inert atmosphere; Enzymatic reaction; optical yield given as %ee; enantioselective reaction;94%
With Novozym 435; In toluene at 70℃; for 48h;
Isopropenyl acetate
108-22-5

Isopropenyl acetate

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

(R)-1-cyclohexylethyl acetate
58396-29-5

(R)-1-cyclohexylethyl acetate

Conditions
ConditionsYield
With dicarbonylchlorido(pentabenzylcyclopentadienyl)ruthenium; potassium tert-butylate; sodium carbonate In tetrahydrofuran; toluene at 23℃; for 3h; Inert atmosphere; dynamic kinetic resolution; Enzymatic reaction; optical yield given as %ee; enantioselective reaction;94%
With Candida antarctica lipase B; potassium phosphate; C38H24O3Ru In toluene at 50℃; for 20h; Molecular sieve; Inert atmosphere; optical yield given as %ee; enantioselective reaction;90%
With Candida antarctica lipase B; potassium phosphate; C38H24O3Ru In toluene at 50℃; for 20h; Dynamic kinetic resolution; Molecular sieve; Inert atmosphere; Enzymatic reaction; optical yield given as %ee;90%
With Candida antarctica lipase B; potassium tert-butylate; sodium carbonate; [chlorodicarbonyl(η-pentaphenylcyclopentadienyl)]Ru(II) In toluene at 20℃; for 17h;98 % Chromat.
Stage #1: Isopropenyl acetate; rac-1-cyclohexylethanol With Novozym 435 In toluene at 60℃; for 1h; Enzymatic reaction;
Stage #2: In toluene at 60℃; for 18h;
n/a
rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

benzoic acid hydrazide
613-94-5

benzoic acid hydrazide

N′-(1-cyclohexylethyl)benzohydrazide
1431943-16-6

N′-(1-cyclohexylethyl)benzohydrazide

Conditions
ConditionsYield
With nickel(II) triflate; 1,3-bis(dicyclohexylphosphine)propane In tert-Amyl alcohol at 120℃; for 24h; Inert atmosphere; Glovebox; Schlenk technique; Molecular sieve;93%
With nickel(II) triflate; 1,1,1,3',3',3'-hexafluoro-propanol; 1,3-bis(dicyclohexylphosphine)propane In tert-Amyl alcohol at 120℃; for 24h; Inert atmosphere; Schlenk technique; Molecular sieve; Sealed tube;93%
rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

(R)-2-(2,4-Dichloro-phenoxy)-propionic acid 1-cyclohexyl-ethyl ester

(R)-2-(2,4-Dichloro-phenoxy)-propionic acid 1-cyclohexyl-ethyl ester

Conditions
ConditionsYield
With dmap; dicyclohexyl-carbodiimide In diethyl ether for 4.5h; Ambient temperature;92%
rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

1,3-dicyclohexylbutan-1-one
27607-65-4

1,3-dicyclohexylbutan-1-one

Conditions
ConditionsYield
With [RuCl2(p-cymene)(iPr2-imy)]; tricyclohexylphosphine tetrafluoroborate; potassium hydroxide In toluene at 110℃; for 24h; Schlenk technique; Inert atmosphere;92%
rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

4-methoxy-aniline
104-94-9

4-methoxy-aniline

(+)-N-(4-methoxyphenyl)-1-(cyclohexyl)ethyl amine

(+)-N-(4-methoxyphenyl)-1-(cyclohexyl)ethyl amine

Conditions
ConditionsYield
With (R)-3,3'-bis(2,4,6-triisopropylphenyl)binol phosphoric acid; (C5(CH3)5)Ir(NHCH(C6H5)CH(C6H5)NSO2C6(CH3)5) In tert-Amyl alcohol for 24h; Inert atmosphere; Glovebox; Molecular sieve; Reflux; enantioselective reaction;92%
rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

1-cyclohexylethyl 4-methylbenzenesulfonate
38293-92-4

1-cyclohexylethyl 4-methylbenzenesulfonate

Conditions
ConditionsYield
With trimethylamine hydrochloride; triethylamine In dichloromethane at 0℃; Inert atmosphere;92%
With dmap; triethylamine In dichloromethane at 20℃; for 2h;86.3%

Conditions
ConditionsYield
With bis-[(trifluoroacetoxy)iodo]benzene In dichloromethane at 20℃; for 2h; Irradiation;92%

Formic acid 1-cyclohexyl-ethyl ester

Formic acid 1-cyclohexyl-ethyl ester

Conditions
ConditionsYield
With p-toluenesulfonyl chloride at 20℃; for 0.166667h; neat (no solvent);91%
With silica triflate In hexane for 0.0833333h; Heating;90%

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

(1-methoxymethoxy-ethyl)-cyclohexane

(1-methoxymethoxy-ethyl)-cyclohexane

Conditions
ConditionsYield
phosphomolybdic acid hydrate at 20℃; for 3.25h;90%
Fe(HSO4)3 at 20℃; for 2.5h;74%
3,4-dihydro-2H-pyran
110-87-2

3,4-dihydro-2H-pyran

rac-1-cyclohexylethanol
1193-81-3

rac-1-cyclohexylethanol

Conditions
ConditionsYield
Stage #1: 3,4-dihydro-2H-pyran With 2Br3(1-)*C18H36N2O6*2H(1+) In acetonitrile at 20℃; for 0.0166667h;
Stage #2: rac-1-cyclohexylethanol In acetonitrile at 20℃; for 0.0666667h;
90%
Stage #1: 3,4-dihydro-2H-pyran With C12H24KO6(1+)*Br3H(1-) In acetonitrile at 20℃; for 0.0166667h;
Stage #2: rac-1-cyclohexylethanol In acetonitrile at 20℃; for 0.666667h;
86%
With Iron(III) nitrate nonahydrate; sodium iodide In dichloromethane at 20℃; for 0.166667h;84%

1-Cyclohexylethanol Chemical Properties

Chemical Name: 1-Cyclohexylethanol
IUPAC NAME: 1-Cyclohexylethanol
CAS No.: 1193-81-3
EINECS: 214-780-7
RTECS: GV5776500
RTECS Class: Primary Irritant
Molecular Formula: C8H16O
Molecular Weight: 128.21 g/mol
Density: 0.884 g/cm3
Flash Point: 80.2 °C
Boiling Point: 192 °C at 760 mmHg
Following is the structure of 1-Cyclohexylethanol (CAS No.1193-81-3):


The chemical synonymous of 1-Cyclohexylethanol (CAS No.1193-81-3) are (R,S)-1-Cyclohexyl-ethanol ; 1-Cyclohexyl-1-ethanol ; 2-Methylcyclohexylmethanol ; alpha-Methyl-cyclohexanemethano ; Cyclohexanemethanol, alpha-methyl- ; Ethanol, 1-cyclohexyl- ; Methanol, cyclohexylmethyl- ; Methylcyclohexylcarbinol

1-Cyclohexylethanol Toxicity Data With Reference

1.    

skn-rbt 500 µL/24H SEV

    NTIS**    National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0545755 .
2.    

eye-rbt 100 µL/24H MLD

    NTIS**    National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0545755 .
3.    

orl-rat LD50:2100 mg/kg

    NTIS**    National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0545755 .
4.    

skn-rbt LDLo:1 g/kg

    NTIS**    National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0545755 .

1-Cyclohexylethanol Safety Profile

Moderately toxic by ingestion and skin contact. A severe skin and mild eye irritant. When heated to decomposition it emits acrid smoke and irritating vapors.
Risk Statements about 1-Cyclohexylethanol (CAS No.1193-81-3):
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements about 1-Cyclohexylethanol (CAS No.1193-81-3):
S23:Do not breathe vapour.
S24/25:Avoid contact with skin and eyes.

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