Home Categories Chemical Reagents 1,1,3,3-Tetramethyldisiloxane
A7723312

1,1,3,3-Tetramethyldisiloxane , 98% , 3277-26-7

Synonym(s):
1,1,3,3-Tetramethyldisiloxane

CAS NO.:3277-26-7

Empirical Formula: C4H14OSi2

Molecular Weight: 134.32

MDL number: MFCD00008256

EINECS: 221-906-4

Pack Size Price Stock Quantity
5ML RMB41.60 In Stock
25ML RMB44.80 In Stock
100ML RMB104.80 In Stock
250ml RMB231.20 In Stock
500ML RMB372.80 In Stock
2.5L RMB1307.20 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: <-78°C
Boiling point: 70-71 °C (lit.)
Density  0.76 g/mL at 25 °C (lit.)
vapor pressure  250 hPa (20 °C)
refractive index  n20/D 1.370(lit.)
Flash point: 14 °F
storage temp.  Store at <= 20°C.
solubility  soluble in Chloroform
pka 11.9[at 20 ℃]
form  liquid
color  colorless
Specific Gravity 0.757
explosive limit 0.8-62.9%(V)
Water Solubility  DECOMPOSES
Sensitive  Moisture Sensitive
Hydrolytic Sensitivity 3: reacts with aqueous base
BRN  1733364
InChIKey NVYQDQZEMGUESH-UHFFFAOYSA-N
LogP -0.38-4.5 at 20-25℃
CAS DataBase Reference 3277-26-7(CAS DataBase Reference)
NIST Chemistry Reference ((CH3)2SiH)2O(3277-26-7)
EPA Substance Registry System Disiloxane, 1,1,3,3-tetramethyl- (3277-26-7)

Description and Uses

1,1,3,3-Tetramethyldisiloxane is soluble in many organic solvents, such as aromatic hydrocarbon and petroleum hydrocarbons, and so on. This product is a kind of widely used organic silicon intermediates, and usually be used as organic silicon blocking agent. Due to containing reactive Si-H groups in the molecular structure, it can be used in the synthesis of copolymer macromolecule by hydrosilylation. The synthesis of copolymer macromolecule can be made into a series of reactive silicone oil.

1, 1, 3, 3-Tetramethyldisiloxane is a kind of siloxane derivative, and can be used as a monomer for the preparation of silicone polymers or silicone resins. It is used as an intermediate for preparing other organosilicon compounds. It is also used in non-aqueous polymer preparation as well as a laboratory reagent. In organic synthesis, it finds an application as an effective reducing agent in platinum-catalyzed reduction of carboxamides to amines as well as in the Au/TiO2-catalyzed hydrosilylation of carbonyl compounds (e.g., reduction of aldehydes or ketones) relative to monohydrosilanes. It can also enable a direct bromination of carboxylic acids in the presence of indium bromide (InBr3) as catalyst.

Safety

Symbol(GHS) 
GHS02
Signal word  Danger
Hazard statements  H225
Precautionary statements  P210-P233-P240-P241-P242-P243
Hazard Codes  F
Risk Statements  11-36/37/38-16
Safety Statements  16-26-36-9-33-29
RIDADR  UN 2924 3/PG 2
WGK Germany  3
RTECS  JN1000000
10-21
Autoignition Temperature 240 °C
TSCA  Yes
HazardClass  3
PackingGroup  II
HS Code  29310095

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