Product Name

  • Name

    Decamethylcyclopentasiloxane

  • EINECS 208-764-9
  • CAS No. 541-02-6
  • Article Data53
  • CAS DataBase
  • Density 0.96 g/cm3
  • Solubility Immiscible with water.
  • Melting Point -44 °C
  • Formula C10H30O5 Si5
  • Boiling Point 210 °C at 760 mmHg
  • Molecular Weight 370.773
  • Flash Point 95.6 °C
  • Transport Information
  • Appearance liquid
  • Safety 23-24/25
  • Risk Codes 36/37/38
  • Molecular Structure Molecular Structure of 541-02-6 (Decamethylcyclopentasiloxane)
  • Hazard Symbols IrritantXi
  • Synonyms Cyclopentasiloxane,decamethyl- (6CI,8CI,9CI);Botanisil CP 33;Cyclic dimethylsiloxane pentamer;Cyclo-decamethylpentasiloxane;Cyclopentadimethylsiloxane;Cyclopentasiloxane;DC 345 Fluid;Dow Corning 345 Fluid;Dow Corning 345EU;Execol D5;KF 995;Pentacyclomethicone;SF1202;SH 245 (siloxane);Silbione 70045V5;Silbione V 5;TFS 405;TSF 465;Union Carbide 7158 Silicone Fluid;VS 7158;Volasil 245;VolatileSilicone Fluid 345;Decamethylcyclopentasiloxane;
  • PSA 46.15000
  • LogP 3.59200

Synthetic route

2,2,4,4,6,6-hexamethyl-8,8-divinylcyclotetrasiloxane
433725-45-2

2,2,4,4,6,6-hexamethyl-8,8-divinylcyclotetrasiloxane

A

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

B

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

C

tetravinyltetramethylcyclotetrasiloxane

tetravinyltetramethylcyclotetrasiloxane

D

copoly(dimethylsiloxane/divinylsiloxane), prepared by anionic polymerization of 2,2,4,4,6,6-hexamethyl-8,8-divinylcyclotetrasiloxane; monomer(s): 2,2,4,4,6,6-hexamethyl-8,8-divinylcyclotetrasiloxane

copoly(dimethylsiloxane/divinylsiloxane), prepared by anionic polymerization of 2,2,4,4,6,6-hexamethyl-8,8-divinylcyclotetrasiloxane; monomer(s): 2,2,4,4,6,6-hexamethyl-8,8-divinylcyclotetrasiloxane

Conditions
ConditionsYield
With P4-t-Bu at 80℃; for 0.333333h; Further byproducts given;A n/a
B n/a
C n/a
D 80%
dimethyl sulfoxide
67-68-5

dimethyl sulfoxide

dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

A

chloro-methylsulfanyl-methane
2373-51-5

chloro-methylsulfanyl-methane

B

Hexamethylcyclotrisiloxane
541-05-9

Hexamethylcyclotrisiloxane

C

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

D

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

E

dodecamethyl-cyclohexasiloxane
540-97-6

dodecamethyl-cyclohexasiloxane

Conditions
ConditionsYield
at 0℃; Mechanism; other diorganyldichlorosilanes; reactions in the presence of hexamethyldisiloxane, trimethylchlorosilane, tetramethoxysilane, tetraethoxysilane;A 79%
B 48%
C 35%
D 12%
E 5%
dimethyl sulfoxide
67-68-5

dimethyl sulfoxide

A

chloro-methylsulfanyl-methane
2373-51-5

chloro-methylsulfanyl-methane

B

Hexamethylcyclotrisiloxane
541-05-9

Hexamethylcyclotrisiloxane

C

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

D

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

Conditions
ConditionsYield
With dimethylsilicon dichloride at 0℃; Further byproducts given;A 79%
B 48%
C 35%
D 5%
phenyltrimethylsilyl ether
1529-17-5

phenyltrimethylsilyl ether

A

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

B

dimethyl-diphenoxy-silane
3440-02-6

dimethyl-diphenoxy-silane

C

C13H26O3Si3
18406-79-6

C13H26O3Si3

D

C11H20O2Si2

C11H20O2Si2

Conditions
ConditionsYield
With gallium(III) iodide at 175 - 180℃; for 3h; Yield given; Further byproducts given. Title compound not separated from byproducts;A n/a
B 79%
C n/a
D n/a
diiododimethylsilane
15576-81-5

diiododimethylsilane

A

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

B

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

Conditions
ConditionsYield
With 3,3-dimethyl-butan-2-one; zinc In dichloromethane for 0.166667h; Ambient temperature;A 60%
B 18%
dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

A

Hexamethylcyclotrisiloxane
541-05-9

Hexamethylcyclotrisiloxane

B

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

C

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

Conditions
ConditionsYield
With pyridine; sodium hydrogencarbonate In ethyl acetate at 20℃; for 3h;A 60%
B 20%
C 15%
With water Autoclave;A 51.3%
B 29.2%
C 8%
With composite catalyst at 150℃; under 675.068 Torr; for 0.5h; Temperature; Pressure; Reagent/catalyst; Large scale;A n/a
B 43%
C n/a
dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

A

Hexamethylcyclotrisiloxane
541-05-9

Hexamethylcyclotrisiloxane

B

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

C

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

D

dodecamethyl-cyclohexasiloxane
540-97-6

dodecamethyl-cyclohexasiloxane

Conditions
ConditionsYield
With dimethyl sulfoxide at 0℃; Further byproducts given;A 48%
B 35%
C 12%
D 5%
With tetrahydrofuran; lithium at 40 - 45℃; for 1h; Yield given. Further byproducts given. Yields of byproduct given;
With hydrogenchloride In toluene at 20℃; for 4h; Yield given. Further byproducts given. Yields of byproduct given;
dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

A

tetradecamethylcycloheptasiloxane
107-50-6

tetradecamethylcycloheptasiloxane

B

Hexamethylcyclotrisiloxane
541-05-9

Hexamethylcyclotrisiloxane

C

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

D

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

E

dodecamethyl-cyclohexasiloxane
540-97-6

dodecamethyl-cyclohexasiloxane

Conditions
ConditionsYield
With H2O In water slow addn. of 4l (CH3)2SiCl2 to 12l H2O at 15-20°C withorous stirring; further products;; distn.;;A n/a
B 0.5%
C 42%
D 6.7%
E 1.6%
With hydrogenchloride In toluene at 20℃; for 4h; Product distribution; diff. concentration of aq. HCl; diff. reaction time; other difunctional organochlorosilanes;
With H2O In diethyl ether; water addn. of (CH3)2SiCl2 to ether-H2O; further products;; distn.;;
dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

A

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

B

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

Conditions
ConditionsYield
With water at 15 - 20℃; Autoclave;A 42%
B 6.7%
trimethyl phosphite
512-56-1

trimethyl phosphite

dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

A

methylene chloride
74-87-3

methylene chloride

B

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

C

dodecamethyl-cyclohexasiloxane
540-97-6

dodecamethyl-cyclohexasiloxane

D

C7H21O6PSi3
1450711-54-2

C7H21O6PSi3

E

C9H27O7PSi4
1450711-55-3

C9H27O7PSi4

Conditions
ConditionsYield
at 20℃; for 10h; Inert atmosphere;A n/a
B 15%
C 10%
D 38%
E 33%
1,1,3,3-Tetramethyldisiloxane
3277-26-7

1,1,3,3-Tetramethyldisiloxane

A

tetradecamethylcycloheptasiloxane
107-50-6

tetradecamethylcycloheptasiloxane

B

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

C

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

D

dodecamethyl-cyclohexasiloxane
540-97-6

dodecamethyl-cyclohexasiloxane

Conditions
ConditionsYield
With iodine In dichloromethane for 0.333333h; Heating; Further byproducts given;A 14%
B 26%
C 21%
D 15%
diethoxy dimethylsilane
78-62-6

diethoxy dimethylsilane

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

Conditions
ConditionsYield
With hydrogenchloride
dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

Conditions
ConditionsYield
With water at 15 - 20℃;
With water Erhitzen der gebildeten nicht destillierbaren Produkte mit NaOH auf 230-240grad unter 1 mm;
Hexamethylcyclotrisiloxane
541-05-9

Hexamethylcyclotrisiloxane

A

tetradecamethylcycloheptasiloxane
107-50-6

tetradecamethylcycloheptasiloxane

B

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

C

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

D

dodecamethyl-cyclohexasiloxane
540-97-6

dodecamethyl-cyclohexasiloxane

Conditions
ConditionsYield
With hydrogenchloride for 72h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
1,1,3,3,5,5,7,7,9,9-decamethylpentasiloxane-1,9-diol
7445-36-5

1,1,3,3,5,5,7,7,9,9-decamethylpentasiloxane-1,9-diol

A

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

B

permethyldecasiloxane-1,19-diol

permethyldecasiloxane-1,19-diol

Conditions
ConditionsYield
With trifluorormethanesulfonic acid In 1,4-dioxane at 35℃; Product distribution; Kinetics; var. of reagent, solvent;
chloro(2-chloroethoxy)dimethylsilane
62806-42-2

chloro(2-chloroethoxy)dimethylsilane

A

Hexamethylcyclotrisiloxane
541-05-9

Hexamethylcyclotrisiloxane

B

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

C

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

Conditions
ConditionsYield
With potassium Sodium at 280 - 300℃; under 0.1 - 1 Torr; Yield given. Yields of byproduct given;
With potassium Sodium In gaseous matrix at 280 - 320℃; under 0.1 - 1 Torr; Product distribution;
2,2,4,4,6,6,8,8,10,10-Decamethyl-[1,3,5,7,9,2,4,6,8,10]pentoxapentasilecane; compound with trifluoro-methanesulfonic acid

2,2,4,4,6,6,8,8,10,10-Decamethyl-[1,3,5,7,9,2,4,6,8,10]pentoxapentasilecane; compound with trifluoro-methanesulfonic acid

4-Chloro-2-nitroaniline
89-63-4

4-Chloro-2-nitroaniline

A

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

B

4-Chloro-2-nitro-phenylamine; compound with trifluoro-methanesulfonic acid

4-Chloro-2-nitro-phenylamine; compound with trifluoro-methanesulfonic acid

Conditions
ConditionsYield
In benzene at 26.9℃; Equilibrium constant;
dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

A

tetradecamethylcycloheptasiloxane
107-50-6

tetradecamethylcycloheptasiloxane

B

Hexamethylcyclotrisiloxane
541-05-9

Hexamethylcyclotrisiloxane

C

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

D

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

Conditions
ConditionsYield
With hydrogenchloride In toluene at 20℃; for 4h; Yield given. Further byproducts given. Yields of byproduct given;
dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

A

tetradecamethylcycloheptasiloxane
107-50-6

tetradecamethylcycloheptasiloxane

B

Hexamethylcyclotrisiloxane
541-05-9

Hexamethylcyclotrisiloxane

C

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

D

dodecamethyl-cyclohexasiloxane
540-97-6

dodecamethyl-cyclohexasiloxane

Conditions
ConditionsYield
With hydrogenchloride In toluene at 20℃; for 4h; Yield given. Further byproducts given. Yields of byproduct given;
dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

A

Hexamethylcyclotrisiloxane
541-05-9

Hexamethylcyclotrisiloxane

B

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

C

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

D

Tetradecamethylcycloheptasilan
13452-94-3

Tetradecamethylcycloheptasilan

E

decamethylcyclopentasilane
13452-92-1

decamethylcyclopentasilane

F

dodecamethylcyclohexasilane
4098-30-0

dodecamethylcyclohexasilane

Conditions
ConditionsYield
With tetrahydrofuran; lithium at 40 - 45℃; Product distribution; Mechanism; various temperature, various reactant ratios;
3,3,6,6,9,9,12,12-Octamethyl-1,2,4,5,7,8,10,11-octaoxa-3,6,9,12-tetrasila-cyclododecane

3,3,6,6,9,9,12,12-Octamethyl-1,2,4,5,7,8,10,11-octaoxa-3,6,9,12-tetrasila-cyclododecane

A

Hexamethylcyclotrisiloxane
541-05-9

Hexamethylcyclotrisiloxane

B

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

C

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

Conditions
ConditionsYield
at 50℃; Product distribution;
trimethylsilyl iodide
16029-98-4

trimethylsilyl iodide

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

A

Octamethyltrisiloxane
107-51-7

Octamethyltrisiloxane

B

decamethyltetrasiloxane
141-62-8

decamethyltetrasiloxane

C

dodecamethylpentasiloxane
141-63-9

dodecamethylpentasiloxane

D

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

Conditions
ConditionsYield
at 190℃; for 10h; Yield given; Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts;
octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

A

Hexamethyldisiloxane
107-46-0

Hexamethyldisiloxane

B

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

C

tetradecamethylhexasiloxane
107-52-8

tetradecamethylhexasiloxane

D

dodecamethyl-cyclohexasiloxane
540-97-6

dodecamethyl-cyclohexasiloxane

Conditions
ConditionsYield
With aluminium(III) iodide at 140 - 170℃; for 5h; Yield given; Title compound not separated from byproducts;A 0.12 g
B n/a
C n/a
D n/a
1,3,5,7,9-pentachloro-1,3,5,7,9-pentamethylcyclopentasiloxane
18139-89-4

1,3,5,7,9-pentachloro-1,3,5,7,9-pentamethylcyclopentasiloxane

methyllithium
917-54-4

methyllithium

A

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

B

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

C

dodecamethyl-cyclohexasiloxane
540-97-6

dodecamethyl-cyclohexasiloxane

Conditions
ConditionsYield
In diethyl ether at 0℃; Product distribution; other organometallic reagent and reaction conditions;
dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

A

1,1,3,3-tetramethyl-1,3-dichlorodisiloxane
2401-73-2

1,1,3,3-tetramethyl-1,3-dichlorodisiloxane

B

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

C

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

D

dodecamethyl-cyclohexasiloxane
540-97-6

dodecamethyl-cyclohexasiloxane

Conditions
ConditionsYield
With sodium nitrate at 0℃; for 2h; Yield given; Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts;
dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

A

Octamethyltrisiloxane
107-51-7

Octamethyltrisiloxane

B

decamethyltetrasiloxane
141-62-8

decamethyltetrasiloxane

C

dodecamethylpentasiloxane
141-63-9

dodecamethylpentasiloxane

D

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

Conditions
ConditionsYield
With sodium nitrate; 1,1,1,3,3,3-hexamethyl-disilazane at 65℃; for 2h; Yield given; Yields of byproduct given. Title compound not separated from byproducts;
With sodium nitrate; 1,1,1,3,3,3-hexamethyl-disilazane at 20℃; for 2h; Yield given; Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts;
dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

A

Octamethyltrisiloxane
107-51-7

Octamethyltrisiloxane

B

decamethyltetrasiloxane
141-62-8

decamethyltetrasiloxane

C

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

D

tetradecamethylhexasiloxane
107-52-8

tetradecamethylhexasiloxane

Conditions
ConditionsYield
With sodium nitrate; 1,1,1,3,3,3-hexamethyl-disilazane at 20℃; for 2h; Yield given; Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts;
dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

A

1,5-dichlorohexamethyltrisiloxane
3582-71-6

1,5-dichlorohexamethyltrisiloxane

B

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

C

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

D

dodecamethyl-cyclohexasiloxane
540-97-6

dodecamethyl-cyclohexasiloxane

Conditions
ConditionsYield
With sodium nitrate at 0℃; for 2h; Yield given; Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts;
dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

A

1,7-dichlorooctamethyltetrasiloxane
2474-02-4

1,7-dichlorooctamethyltetrasiloxane

B

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

C

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

D

dodecamethyl-cyclohexasiloxane
540-97-6

dodecamethyl-cyclohexasiloxane

Conditions
ConditionsYield
With sodium nitrate at 0℃; for 2h; Yield given; Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts;
dimethylsilicon dichloride
75-78-5

dimethylsilicon dichloride

A

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

B

1,9-dichlorodecamethylpentasiloxane
14741-59-4

1,9-dichlorodecamethylpentasiloxane

C

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

D

dodecamethyl-cyclohexasiloxane
540-97-6

dodecamethyl-cyclohexasiloxane

Conditions
ConditionsYield
With sodium nitrate at 0℃; for 2h; Yield given; Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts;
Li[Al(perfluoro-tertbutoxide)4]

Li[Al(perfluoro-tertbutoxide)4]

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

Li(dimethylsiloxane)5[Al(OC(CF3)3)4]
896439-19-3

Li(dimethylsiloxane)5[Al(OC(CF3)3)4]

Conditions
ConditionsYield
In dichloromethane in Schlenk flask; mixed soln. concd. to saturation by stirring overnightat room temp.; stand for 1 d at -20°C; solvent removed under vac.; washed 3 times with n-hexane; elem. anal.;90%
decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

diisobutylaluminium hydride
1191-15-7

diisobutylaluminium hydride

(H(CH3)2Si(OAl(CH2CH(CH3)2)2)2Si(CH3)2)2O
254763-51-4

(H(CH3)2Si(OAl(CH2CH(CH3)2)2)2Si(CH3)2)2O

Conditions
ConditionsYield
In n-heptane stirring (3 d); evapn.; elem. anal.;84%
decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

dimethylaluminum hydride
865-37-2

dimethylaluminum hydride

(CH3)2Si((OAl(CH3)2)2Si(CH3)2H)2
254763-44-5

(CH3)2Si((OAl(CH3)2)2Si(CH3)2H)2

Conditions
ConditionsYield
In hexane stirring (4 d); evapn. (vac.); elem. anal.;68%
tetrahydrofuran
109-99-9

tetrahydrofuran

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

di(tert-butyl)aluminium hydride
70776-29-3

di(tert-butyl)aluminium hydride

HSi(CH3)2(OAl(C(CH3)3)2)2(Si(CH3)2O)2Al(C4H8O)(C(CH3)3)2
254763-53-6

HSi(CH3)2(OAl(C(CH3)3)2)2(Si(CH3)2O)2Al(C4H8O)(C(CH3)3)2

Conditions
ConditionsYield
In hexane stirring (3 d); filtering, recrystn. (hexane, -23°C); elem. anal.;66%
1,1,3,3-Tetramethyldisiloxane
3277-26-7

1,1,3,3-Tetramethyldisiloxane

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

1,1,3,3,5,5,7,7,9,9,11,11,13,13-tetradecamethylheptasiloxane
19095-23-9

1,1,3,3,5,5,7,7,9,9,11,11,13,13-tetradecamethylheptasiloxane

Conditions
ConditionsYield
With potassium hydroxide In water; toluene at 50℃; for 2h;61%
1,1,3,3-tetraethoxy-1,3-dimethyldisiloxane
18001-60-0

1,1,3,3-tetraethoxy-1,3-dimethyldisiloxane

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

1,3,3,5-tetramethyl-1,1,5,5-tetraethoxytrisiloxane

1,3,3,5-tetramethyl-1,1,5,5-tetraethoxytrisiloxane

Conditions
ConditionsYield
With cesium hydroxide at 100 - 130℃;58%
1,1,3,3-Tetramethyldisiloxane
3277-26-7

1,1,3,3-Tetramethyldisiloxane

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

A

iododimethylsilane
2441-21-6

iododimethylsilane

B

dodecamethyl-cyclohexasiloxane
540-97-6

dodecamethyl-cyclohexasiloxane

Conditions
ConditionsYield
With iodineA n/a
B 50%
dimethylmonochlorosilane
1066-35-9

dimethylmonochlorosilane

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

1,1,3,3,5,5,7,7,9,9,11,11,13,13-tetradecamethylheptasiloxane
19095-23-9

1,1,3,3,5,5,7,7,9,9,11,11,13,13-tetradecamethylheptasiloxane

Conditions
ConditionsYield
With water; sulfur dioxide In hexane Ambient temperature;45%
decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

di(tert-butyl)aluminium hydride
70776-29-3

di(tert-butyl)aluminium hydride

(H(CH3)2Si(OAl(C(CH3)3)2)2Si(CH3)2)2O
254763-49-0

(H(CH3)2Si(OAl(C(CH3)3)2)2Si(CH3)2)2O

Conditions
ConditionsYield
In hexane stirring (4 d); filtering, evapn. (vac.), recrystn. (pentane, -78°C);;44%
silver hexafluoroantimonate

silver hexafluoroantimonate

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

A

Ag(1+)*[((CH3)2SiO)6]=[((CH3)2SiO)6Ag](1+)

Ag(1+)*[((CH3)2SiO)6]=[((CH3)2SiO)6Ag](1+)

B

[((CH3)2SiO)7Ag](1+)*SbF6(1-)=[((CH3)2SiO)7Ag][SbF6]
945917-62-4

[((CH3)2SiO)7Ag](1+)*SbF6(1-)=[((CH3)2SiO)7Ag][SbF6]

Conditions
ConditionsYield
In sulfur dioxide Ag. compd treated with ligand (3.6:2.58 molar ratio), cooled to 77 K, SO2 added, warmed to room temp., pptd.; filtered off, MAS, NMR;A n/a
B 23%
decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

cyclomaltooctaose
17465-86-0

cyclomaltooctaose

C10H30O5Si5*4C48H80O40

C10H30O5Si5*4C48H80O40

Conditions
ConditionsYield
In water at 20℃; Sonication;11%
decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

2,7-dimethyl-2,3:7,8-diepoxy-5-silaspiro<4.4>nonane
63683-92-1

2,7-dimethyl-2,3:7,8-diepoxy-5-silaspiro<4.4>nonane

2,2,4,4,8,8,10,10,12,12-decamethyl-2,4,6,8,10,12-hexasila-1,3,5,7,9,11,13-heptaoxaspiro<5.7>tridecane
17995-45-8

2,2,4,4,8,8,10,10,12,12-decamethyl-2,4,6,8,10,12-hexasila-1,3,5,7,9,11,13-heptaoxaspiro<5.7>tridecane

Conditions
ConditionsYield
at 520℃; under 0.0001 Torr; for 3.25h;9%
decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

A

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

B

dodecamethyl-cyclohexasiloxane
540-97-6

dodecamethyl-cyclohexasiloxane

Conditions
ConditionsYield
With dodecylbenzene-sulphonic acid; acetic acid at 120℃; for 4 - 24h; Product distribution / selectivity;A 1.08%
B 2.05%
With toluene-4-sulfonic acid at 120℃; for 4 - 24h; Product distribution / selectivity;A 0.56%
B 0.59%
With molecular sieve; dodecylbenzene-sulphonic acid at 20 - 120℃; for 0.014 - 24h; Product distribution / selectivity;A 0%
B 0%
With molecular sieve at 20 - 120℃; for 0.017 - 24h; Product distribution / selectivity;A 0.67%
B 0.92%
With acetic acid at 120℃; for 4 - 24h; Product distribution / selectivity;A 0.1%
B 0.48%
decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

dodecamethyl-cyclohexasiloxane
540-97-6

dodecamethyl-cyclohexasiloxane

Conditions
ConditionsYield
With toluene-4-sulfonic acid at 20 - 120℃; for 0.017 - 24h; Product distribution / selectivity;0.68%
With dodecylbenzene-sulphonic acid at 20 - 120℃; for 0.017 - 24h; Product distribution / selectivity;0.74%
With dodecylbenzene-sulphonic acid at 20 - 120℃; for 0.017 - 24h; Product distribution / selectivity;0.7%
decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

octamethylcyclotetrasiloxane
556-67-2

octamethylcyclotetrasiloxane

Conditions
ConditionsYield
With hydrogenchloride at 120℃; for 4 - 24h; Product distribution / selectivity;0.1%
decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

dimethyldifluorosilane
353-66-2

dimethyldifluorosilane

Conditions
ConditionsYield
With hydrogen fluoride; copper(II) sulfate
dimethylmonochlorosilane
1066-35-9

dimethylmonochlorosilane

decamethylcyclopentasiloxane
541-02-6

decamethylcyclopentasiloxane

1-chloro-1,1,3,3,5,5,7,7,9,9,11,11-dodecamethylhexasiloxane
132118-77-5

1-chloro-1,1,3,3,5,5,7,7,9,9,11,11-dodecamethylhexasiloxane

Conditions
ConditionsYield
With water; pyrographite for 5h; Ambient temperature; Yield given;

Decamethylcyclopentasiloxane Consensus Reports

Decamethylcyclopentasiloxane(541-02-6) is reported in EPA TSCA Inventory.

Decamethylcyclopentasiloxane Specification

The Decamethylcyclopentasiloxane, with the cas register number 541-02-6, has its systematic name of 2,2,4,4,6,6,8,8,10,10-decamethyl-1,3,5,7,9,2,4,6,8,10-pentoxapentasilecane. This is a kind of liquid, and incompatible with strong oxidizing agents. And its product categories are various, including siloxanes;organics;si (classes of silicon compounds);si-o compounds;organometallic reagents;organosilicon. As to its usage, it is widely applied in the cosmetic and personal nursing care products.

The characteristics of  Decamethylcyclopentasiloxane are as follows: (1)#H bond acceptors: 5; (2)Polar Surface Area: 46.15; (3)Index of Refraction: 1.427; (4)Molar Refractivity: 98.78 cm3; (5)Molar Volume: 384.3 cm3; (6)Polarizability: 39.16 ×10-24 cm3; (7)Surface Tension: 19 dyne/cm; (8)Density: 0.96 g/cm3; (9)Flash Point: 95.6 °C; (10)Enthalpy of Vaporization: 42.81 kJ/mol; (11)Boiling Point: 210 °C at 760 mmHg; (12)Vapour Pressure: 0.285 mmHg at 25°C; (13)Exact Mass: 370.093957; (14)MonoIsotopic Mass: 370.093957; (15)Topological Polar Surface Area: 46.2; (16)Heavy Atom Count: 20; (17)Complexity: 258.

Use of Decamethylcyclopentasiloxane: Decamethylcyclopentasiloxane reacts with chloro-dimethyl-silane  to produce 1,13-Dihydrotetradecamethylheptasiloxan, with the following condition: reagent: H2O; catalytic agent: SO2; solution: hexane; yield: 45%; other condition: ambient temperature.

Production method of Decamethylcyclopentasiloxane: Diiodo-dimethyl-silane reacts with octamethyl-cyclotetrasiloxane to produce Decamethylcyclopentasiloxane, with the following condition: reagent: pinacolone, Zn; solution: CH2Cl2; reaction time: 10 min; yield: 60%; other condition: ambient temperature.

While dealing with Decamethylcyclopentasiloxane, you should be very cautious. For being a kind of harmful chemical, it may cause damage to health, and it has limited evidence of a carcinogenic effect. Therefore, you had better wear suitable protective clothing while using this chemical and remember not to breathe dust. 

In addition, you could obtain the molecular structure by converting the following datas:
(1)SMILES:O1[Si](O[Si](O[Si](O[Si](O[Si]1(C)C)(C)C)(C)C)(C)C)(C)C;
(2)Std. InChI:InChI=1S/C10H30O5Si5/c1-16(2)11-17(3,4)13-19(7,8)15-20(9,10)14-18(5,6)12-16/h1-10H3 CopyCopied ;
(3)Std. InChIKey:XMSXQFUHVRWGNA-UHFFFAOYSA-N.

Below are the toxicity information of Decamethylcyclopentasiloxane:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
rabbit LD50 skin > 16mL/kg (16mL/kg)   Toxicology and Applied Pharmacology. Vol. 28, Pg. 313, 1974.
 
rat LC inhalation > 2700mg/m3/4H (2700mg/m3)   National Technical Information Service. Vol. OTS0572802,
rat LD50 oral > 24134mg/kg (24134mg/kg)   National Technical Information Service. Vol. OTS0572801,

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