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1,1,3,3-Tetramethyldisilazane

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Products Intro: Product Name:Tetramethyldisilazane
CAS:15933-59-2
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Products Intro: Product Name:1,1,3,3-Tetramethyldisilazane
CAS:15933-59-2
Purity:98% Package:1KG;5USD|1000KG;0.1USD
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CAS:15933-59-2
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Products Intro: Product Name:1,1,3,3-TETRAMETHYLDISILAZANE
CAS:15933-59-2
Purity:99% Package:25KG;5KG;1KG
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Products Intro: Product Name:1,1,3,3-TETRAMETHYLDISILAZANE
CAS:15933-59-2
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G

1,1,3,3-Tetramethyldisilazane manufacturers

  • Tetramethyldisilazane
  • Tetramethyldisilazane pictures
  • $5.00 / 1KG
  • 2023-03-06
  • CAS:15933-59-2
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 10000kg
  • Tetramethyldisilazane
  • Tetramethyldisilazane pictures
  • $7.98/ L
  • 2022-11-12
  • CAS:15933-59-2
  • Min. Order: 25L
  • Purity: 92%
  • Supply Ability: 18000 L per year
1,1,3,3-Tetramethyldisilazane Basic information
Product Name:1,1,3,3-Tetramethyldisilazane
Synonyms:Silanamine, N-(dimethylsilyl)-1,1-dimethyl-;1,1,3,3-TETRAMETHYLDISILAZANE;N-(dimethylsilyl)-1,1-dimethylsilylamine;TETRAMETHYLDISILAZANE 98+%;1,1,3,3-Tetramethyl-2-azatrisilane;Disilazane, 1,1,3,3-tetramethyl-;N-(Dimethylsilyl)(dimethyl)silanamine;n-(dimethylsilyl)-1,1-dimethyl-silanamin
CAS:15933-59-2
MF:C4H15NSi2
MW:133.34
EINECS:240-072-2
Product Categories:Chemical Synthesis;Organometallic Reagents;Organosilicon;Analytical Chemistry;Dimethylsilylation (GC Derivatizing Reagents);GC Derivatizing Reagents;Si (Classes of Silicon Compounds);Si-H Compounds;Silazanes;Silylation (GC Derivatizing Reagents);Si-N Compounds
Mol File:15933-59-2.mol
1,1,3,3-Tetramethyldisilazane Structure
1,1,3,3-Tetramethyldisilazane Chemical Properties
Melting point 99-100 °C
Boiling point 99-100 °C
density 0.752 g/mL at 25 °C(lit.)
refractive index n20/D 1.404(lit.)
Fp 17 °F
storage temp. Store below +30°C.
solubility Miscible with common organic solvents.
pka9.80±0.70(Predicted)
form clear liquid
color Colorless to Almost colorless
Specific Gravity0.752
Sensitive Moisture Sensitive
Hydrolytic Sensitivity7: reacts slowly with moisture/water
BRN 741869
CAS DataBase Reference15933-59-2(CAS DataBase Reference)
EPA Substance Registry SystemSilanamine, N-(dimethylsilyl)-1,1-dimethyl- (15933-59-2)
Safety Information
Hazard Codes F,Xi
Risk Statements 11-36/37/38
Safety Statements 16-26-36
RIDADR UN 2924 3/PG 2
WGK Germany 3
10-21
TSCA Yes
HazardClass 3
PackingGroup II
HS Code 29319090
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
1,1,3,3-Tetramethyldisilazane Usage And Synthesis
Chemical PropertiesClear colorless to faintly yellow liquid
Physical propertiesbp 99–100 °C; n20 D 1.4040; d 0.752 g cm?3.
UsesTetramethyldisilazane is used as a gas chromatographic derivatizing reagent. Further, it reacts with phenol to prepare dimethylphenoxysilane. In addition, it is used in electronic, polymer and pharmaceutical industries.
Uses1,1,3,3-Tetramethyldisilazane is widely used in intramolecular hydrosilation of allyl alcohols, homoallyl alcohols, and homopropargyl alcohols for the regio- and stereoselective synthesis of polyols
Properties and ApplicationsThe ICP CVD synthesis of SiCxNy: H thin films using 1,1,3,3-tetramethyldisilazane (TMDSZ ) as a single-source precursor and argon as a gas-activator[1]. Using TMDSZ as the single-source compound produced amorphous hydrogenated silicon carbonitride (a-SiCN: H) films, whereas no such films were formed when HMDSZ was used, which was attributed to the lack of Si–H bond in HMDSZ. Under the collision-free condition, the formation of ?CH3, NH3, and DMSA was demonstrated from the decomposition of TMDSZ on the heated W filament. Free-radical short-chain reactions dominate the secondary gas-phase reactions of TMDSZ in the reactor setup. The short-chain reaction is initiated by the formation of methyl radicals via the cleavage of the Si–CH3 bonds of TMDSZ. The H abstraction by the produced methyl radicals from the Si–H or the C–H bond in various stable molecules (e.g., TMDSZ) propagates the chain with a resulting radical, which recombines with another radical to terminate the chain reactions, producing a series of products in the high-mass region[2].
References[1] Maksim N. Chagin. “Synthesis, Properties and Aging of ICP-CVD SiCxNy:H Films Formed from Tetramethyldisilazane.” Coatings (2022).
[2] James Michael Stevenson, Eric Ampong and Yujun Shi*. “Understanding the Reaction Chemistry of 1,1,3,3-Tetramethyldisilazane as a Precursor Gas in a Catalytic Chemical Vapor Deposition Process.” The Journal of Physical Chemistry A 127 44 (2023): 9185–9195.
1,1,3,3-Tetramethyldisilazane Preparation Products And Raw materials
Tag:1,1,3,3-Tetramethyldisilazane(15933-59-2) Related Product Information
Tetramethylammonium nitrate (S,S)-(-)-2,3-DIHYDROXY-N,N,N',N'-TETRAMETHYLSUCCINAMIDE TETRAMETHYL-1,3-CYCLOBUTANEDIONE TETRAMETHYLSUCCINONITRILE 2,2,6,6-Tetramethyl-4-piperidinol TETRAMETHYLAMMONIUM HYDROGENSULFATE Octamethylcyclotetrasilazane 1,3-BIS(CHLOROMETHYL)TETRAMETHYLDISILAZANE Lithium bis(trimethylsilyl)amide 2,2,4,4,6,6-Hexamethylcyclotrisilazane 1,3-DIMETHYL-1,1,3,3-TETRAPHENYLDISILAZANE Hexamethyldisilazane 1,1,3,3-Tetramethyl-1,3-divinyldisilazane HEPTAMETHYLDISILAZANE Sodium bis(trimethylsilyl)amide N,N-Bis(trimethylsilyl)formamide NONAMETHYLTRISILAZANE 1,1,3,3-Tetramethyldisilazane