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Phenyltris(trimethylsiloxy)silane, also known as Phenyl Trimethicone, is a polymethylsiloxane derivative of silica that enhances the performance of various cosmetic formulations. It is known for its resistance to oxidation and excellent compatibility with cosmetic ingredients, making it a versatile and valuable component in the beauty and personal care industry.

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  • 2116-84-9 Phenyl trimethicone silicone oil for cosmetic/ personal care products equal to Dow Corning Chemicals DC 556

    Cas No: 2116-84-9

  • USD $ 1500.0-1500.0 / Kilogram

  • 100 Kilogram

  • 10 Metric Ton/Month

  • Hebei yanxi chemical co.,LTD.
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  • 2116-84-9 Structure
  • Basic information

    1. Product Name: Phenyltris(trimethylsiloxy)silane
    2. Synonyms: PHENYL-TRIS(TRIMETHYLSILOXY)SILANE;TRIS(TRIMETHYLSILOXY)PHENYLSILANE;1,1,1,5,5,5-Hexamethyl-3-phenyl-3-(trimethylsilyloxy)trisiloxane;1,1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]-trisiloxan;1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane;DC556;DowCorning556;DowCorning556Fluid
    3. CAS NO:2116-84-9
    4. Molecular Formula: C15H32O3Si4
    5. Molecular Weight: 372.75
    6. EINECS: 218-320-6
    7. Product Categories: Organics;Organometallic Reagents;Organosilicon;Siloxanes;Organic silicon chemicals
    8. Mol File: 2116-84-9.mol
  • Chemical Properties

    1. Melting Point: -102°C
    2. Boiling Point: 264 °C(lit.)
    3. Flash Point: 127°C
    4. Appearance: /
    5. Density: 0.921 g/mL at 20 °C(lit.)
    6. Vapor Pressure: 0.000812mmHg at 25°C
    7. Refractive Index: n20/D 1.437
    8. Storage Temp.: Inert atmosphere,Room Temperature
    9. Solubility: N/A
    10. Water Solubility: 6.6μg/L at 23℃
    11. CAS DataBase Reference: Phenyltris(trimethylsiloxy)silane(CAS DataBase Reference)
    12. NIST Chemistry Reference: Phenyltris(trimethylsiloxy)silane(2116-84-9)
    13. EPA Substance Registry System: Phenyltris(trimethylsiloxy)silane(2116-84-9)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36
    4. WGK Germany: 1
    5. RTECS:
    6. F: 10-21
    7. TSCA: Yes
    8. HazardClass: N/A
    9. PackingGroup: N/A
    10. Hazardous Substances Data: 2116-84-9(Hazardous Substances Data)

2116-84-9 Usage

Uses

Used in Cosmetics and Personal Care Industry:
Phenyltris(trimethylsiloxy)silane is used as an anti-foaming agent for reducing the tendency of formulas to generate foam when shaken. This application is particularly useful in skin lotions and creams, suntan lotions and sprays, and pre-shave lotions, providing a smoother and more comfortable experience for users.
Used in Skin Care Products:
Phenyltris(trimethylsiloxy)silane is used as a skin-conditioning agent, improving the texture of the skin and reducing tackiness and stickiness of organic ingredients in formulations. This enhances the overall feel and performance of skin care products, making them more appealing to consumers.
Used in Hair Care Products:
Phenyltris(trimethylsiloxy)silane is used as a hair conditioning agent, increasing hair's body, suppleness, and sheen. It is particularly effective in hair sprays, conditioners, and grooming brighteners, where it helps to improve the texture of hair that has been damaged by chemical treatments.
Used in Make-up Products:
Phenyltris(trimethylsiloxy)silane is used as an ingredient in make-up products, such as lipstick and foundation, to enhance the dispersion effect of opaque materials. This results in a more even and long-lasting application, providing a better overall appearance for users.

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 2116-84-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,1 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2116-84:
(6*2)+(5*1)+(4*1)+(3*6)+(2*8)+(1*4)=59
59 % 10 = 9
So 2116-84-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H32O3Si4/c1-19(2,3)16-22(17-20(4,5)6,18-21(7,8)9)15-13-11-10-12-14-15/h10-14H,1-9H3

2116-84-9Synthetic route

chloro-trimethyl-silane
75-77-4

chloro-trimethyl-silane

phenyltri(benzyloxy)silane

phenyltri(benzyloxy)silane

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane
2116-84-9

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane

Conditions
ConditionsYield
With 5%-palladium/activated carbon In ethyl acetate at 20℃; for 12h;94%
With palladium 10% on activated carbon In ethyl acetate at 20℃; for 9h; Inert atmosphere;89 %Spectr.
With 10 mol% palladium on carbon In ethyl acetate at 20℃; for 24h;89 %Spectr.
trimethylsilyl acrylate
13688-55-6

trimethylsilyl acrylate

phenyltriallyloxysilane
17938-35-1

phenyltriallyloxysilane

A

allyl acrylate
999-55-3

allyl acrylate

B

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane
2116-84-9

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane

Conditions
ConditionsYield
With ammonium trifluoromethanesulfonate; 4-methoxy-phenol at 60℃; for 8h;A 93.7%
B n/a
trimethylsilan
993-07-7

trimethylsilan

Phenyltrichlorosilane
98-13-5

Phenyltrichlorosilane

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane
2116-84-9

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane

Conditions
ConditionsYield
Stage #1: trimethylsilan With dihydrogen peroxide In toluene at 20℃; for 1.5h;
Stage #2: Phenyltrichlorosilane With triethylamine In toluene for 2h;
93%
chloro-trimethyl-silane
75-77-4

chloro-trimethyl-silane

phenylsilanetriol
3047-74-3

phenylsilanetriol

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane
2116-84-9

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane

Conditions
ConditionsYield
With pyridine In toluene for 7h; Heating;84.6%
1,1,1-trimethyl-3-phenyl-3,3-difluorodisiloxane
34136-85-1

1,1,1-trimethyl-3-phenyl-3,3-difluorodisiloxane

A

trimethylsilyl fluoride
420-56-4

trimethylsilyl fluoride

B

phenyltrifluorosilane
368-47-8

phenyltrifluorosilane

C

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane
2116-84-9

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane

D

C18H28F2O3Si4

C18H28F2O3Si4

Conditions
ConditionsYield
at 20℃; Further byproducts given;
1,1,1-trimethyl-3-phenyl-3,3-difluorodisiloxane
34136-85-1

1,1,1-trimethyl-3-phenyl-3,3-difluorodisiloxane

A

phenyltrifluorosilane
368-47-8

phenyltrifluorosilane

B

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane
2116-84-9

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane

C

1,1,1,5,5,5-hexamethyl-3-phenyl-3-fluorotrisiloxane
34136-84-0

1,1,1,5,5,5-hexamethyl-3-phenyl-3-fluorotrisiloxane

D

C18H28F2O3Si4

C18H28F2O3Si4

Conditions
ConditionsYield
at 20℃; Further byproducts given;
1,1,1-trimethyl-3-phenyl-3,3-difluorodisiloxane
34136-85-1

1,1,1-trimethyl-3-phenyl-3,3-difluorodisiloxane

A

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane
2116-84-9

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane

B

1,1,1,5,5,5-hexamethyl-3-phenyl-3-fluorotrisiloxane
34136-84-0

1,1,1,5,5,5-hexamethyl-3-phenyl-3-fluorotrisiloxane

C

1,1,3,3-tetrafluoro-1,3-diphenyl-1,3-disiloxane
34224-10-7

1,1,3,3-tetrafluoro-1,3-diphenyl-1,3-disiloxane

D

C18H28F2O3Si4

C18H28F2O3Si4

Conditions
ConditionsYield
at 20℃; Further byproducts given;
Phenyltrichlorosilane
98-13-5

Phenyltrichlorosilane

sodium trimethylsilanolate

sodium trimethylsilanolate

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane
2116-84-9

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane

phenyl trimethylsiloxane
2996-92-1

phenyl trimethylsiloxane

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane
2116-84-9

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 68 percent / acetic acid / H2O / 4 h / 5 - 10 °C
2: 84.6 percent / pyridine / toluene / 7 h / Heating
View Scheme
sodium trimethylsilanolate
18027-10-6

sodium trimethylsilanolate

Phenyltrichlorosilane
98-13-5

Phenyltrichlorosilane

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane
2116-84-9

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane

Conditions
ConditionsYield
In pyridine
In pyridine
Phenyltrichlorosilane
98-13-5

Phenyltrichlorosilane

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane
2116-84-9

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: 4-methoxy-phenol / hexane / 4 h / 70 °C
1.2: 0.5 h
2.1: ammonium trifluoromethanesulfonate; 4-methoxy-phenol / 8 h / 60 °C
View Scheme
Trimethylsilanol
1066-40-6

Trimethylsilanol

phenylsilane
694-53-1

phenylsilane

A

C9H16OSi2

C9H16OSi2

B

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane
2116-84-9

1,1,5,5,5-hexamethyl-3-phenyl-3-[(trimethylsilyl)oxy]trisiloxane

Conditions
ConditionsYield
With sodium triethylborohydride In tetrahydrofuran at 20℃; for 12h; Catalytic behavior; Inert atmosphere; Schlenk technique; Glovebox;A 55 %Spectr.
B 30 %Spectr.

2116-84-9Downstream Products

2116-84-9Relevant articles and documents

Selective hydrosiloxane synthesis: Via dehydrogenative coupling of silanols with hydrosilanes catalysed by Fe complexes bearing a tetradentate PNNP ligand

Takeshita, Tomohiro,Sato, Kazuhiko,Nakajima, Yumiko

, p. 17004 - 17010 (2019/01/03)

A well-defined iron complex system was established using PNNP-R (R = Ph and Cy) as a strong σ-donating ligand with a rigid meridional tetradentate structure. Reactive Fe(0) complexes [{Fe(PNNP-R)}2(μ-N2)] were synthesized by a reaction of the corresponding iron dihalide with NaBEt3H and structurally characterized. The reaction proceeded via the iron dihydride intermediate [Fe(H)2(PNNP-R)], which underwent H2 reductive elimination, supporting the hemilabile behavior of PNNP-R. [{Fe(PNNP-R)}2(μ-N2)] catalyzed the dehydrogenative coupling of silanols with silanes to selectively form various hydrosiloxanes, which are important building blocks for the synthesis of a range of siloxane compounds. This system exhibited higher catalytic efficiency than the previously reported precious-metal-catalyzed systems.

Method for synthesize aryltris (tri-R-siloxanyl) silane

-

Paragraph 0025; 0026, (2019/01/08)

The invention relates to the technical field of organic chemistry. In order to solve the problem of complex steps in the process of synthesizing aryltris (tri-R-siloxanyl) silane,the invention provides a method for synthesizing aryltris (tri-R-siloxanyl) silane. An organic solvent is used as solvent, trialkylsilane and hydrogen peroxide react for 1-2 hours, then triethylamine and aryltrichlorosilane are respectively added, and the mixture is allowed to react for 1-5 hours, organic phase is filtered and concentrated to obtain aryltris (tri-R-siloxanyl) silane. The method adopts one pot reaction, which has the advantages of mild conditions, high yield and high product purity, and the process is simple.

Synthetic method of allyl acrylate

-

, (2017/04/28)

The invention discloses a new synthetic method of allyl acrylate. According to the method, an organic silicon monomer with functional groups is used, and the allyl acrylate is prepared under the soft reaction condition. The synthetic method of the allyl acrylate includes three steps that (1) acryloxytrimethylsilane is synthesized; (2) allyloxy silane is synthesized; and (3) the acryloxytrimethylsilane and the allyloxy silane are mixed. According to the raw materials used in a reaction, chlorine elements are fully converted into inorganic salt, low-boiling-point chloride like phosphorus trichloride is not used, and it is guaranteed that the chlorine elements are not contained in a prepared product; reaction conditions are soft, and the requirement for the equipment is not high; purification is easy, boiling points of all components are large in difference, and reduced pressure distillation separation is easy; water washing is not needed, and amplification is easy; and trifluoromethanesulfonic acid serves as a catalyst, the high acidity is achieved, and double bonds cannot be damaged.

Method for producing polyimidesiloxane

-

Paragraph 0046, (2018/10/16)

PROBLEM TO BE SOLVED: To provide a method for synthesizing siloxanes at will in good yield while maintaining high structural controllability, which can be applied to substrates having various substituents.SOLUTION: The method comprises reacting benzyloxysilanes and silicon halides in the absence of hydrogen using a catalyst comprising a transition metal or a compound thereof, preferably a metal of group 9 or group 10 of the periodic table or a compound thereof. Thereby, corresponding siloxanes can be produced safely and simply in high yield under a mild reaction condition accompanied by elimination of a benzyl halide. Especially, by using an active carbon-supported catalyst as a heterogeneous catalyst, the target siloxanes can be separated easily.

In a method of manufacturing a condition anhyride silanolated

-

Paragraph 0034, (2018/03/24)

PROBLEM TO BE SOLVED: To provide a method capable of synthesizing silanol under an anhydrous condition and a mild condition, adapting to substrates having various substituents, and producing siloxanes freely at an excellent yield, while having high structure controllability.SOLUTION: By a hydrogen addition reaction in which benzyloxy-substituted silanes are used as a silanol precursor, and a metal in the group 9 or 10 on the periodic table or a metal compound is used as a catalyst, corresponding silanols can be produced safely and easily at a high yield under an anhydrous condition and a mild condition, and especially object silanols can be isolated easily by using a carbon-carrying catalyst.

Pd/C-catalyzed cross-coupling reaction of benzyloxysilanes with halosilanes for selective synthesis of unsymmetrical siloxanes

Igarashi, Masayasu,Kubo, Keiko,Matsumoto, Tomohiro,Sato, Kazuhiko,Ando, Wataru,Shimada, Shigeru

, p. 19099 - 19102 (2014/05/20)

A new protocol for the nonhydrolytic synthesis of unsymmetrical siloxanes has been developed. The cross-coupling reaction of benzyloxysilanes with halosilanes catalyzed by Pd/C afforded various unsymmetrical siloxanes with co-production of benzyl halides. the Partner Organisations 2014.

Cosmetic composition comprising a volatile fatty phase

-

, (2008/06/13)

The invention relates to a composition comprising, in a physiologically acceptable medium, a volatile silicone fatty phase comprising at least one non-cyclic volatile silicone oil, wherein the volatile silicone fatty phase has an evaporation profile such that the mass of the at least one volatile silicone oil evaporated after 30 minutes is from 2 mg/cm2 to 9 mg/cm2. The invention also relates to making up and caring for human keratin materials using the inventive compositions.

Phenylsilanetriol - Synthesis, stability, and reactivity

Korkin,Buzin,Matukhina,Zherlitsyna,Auner,Shchegolikhina

, p. 313 - 320 (2007/10/03)

Crystalline phenylsilanetriol, PhSi(OH)3 (1) was obtained by smooth hydrolysis of phenyltrimethoxysilane and characterised by different analytical methods (wide angle X-ray powder diffraction, NMR, IR, thermogravimetric analysis). The title-compound is surprisingly stable in the solid state but slowly condenses in acetone solution. Reaction of 1 with Me3SiCl and Me2(CH2 Cl)SiCl gave the corresponding tris-triorganylsiloxy substituted derivatives in high yields.

Method for the cleavage of organic siloxanes, and products and applications thereof

-

, (2008/06/13)

A method for the cleavage of organosiloxanes with chlorosilanes in the presence of ferric chloride and hydrogen chloride as catalysts resulting in chloroalkyl silanes or chloroaryl silanes, and organosiloxanes, which are characterized by one or more --O--Si--R3 groups, (R=alkyl or aryl), which are directly bound to a silicon atom which in turn is bound either to the same grouping or to an alkyl or aryl moiety.

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