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233803

Sigma-Aldrich

3-(Trimethylsilyl)-1-propanol

97%

Synonym(s):

1-(Trimethylsilyl)-3-propanol, 3-(Trimethylsilyl)-1-propanol, 3-(Trimethylsilyl)propanol, 3-(Trimethylsilyl)propyl alcohol, 3-Hydroxypropyltrimethylsilane

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About This Item

Linear Formula:
(CH3)3Si(CH2)3OH
CAS Number:
2917-47-7
Molecular Weight:
132.28
MDL number:
MFCD00009712
UNSPSC Code:
12352100
PubChem Substance ID:
24854012
NACRES:
NA.22

Quality Level

100

Assay

97%

refractive index

n20/D 1.428 (lit.)

bp

111-112 °C/96 mmHg (lit.)

density

0.832 g/mL at 25 °C (lit.)

SMILES string

C[Si](C)(C)CCCO

InChI

1S/C6H16OSi/c1-8(2,3)6-4-5-7/h7H,4-6H2,1-3H3

InChI key

YNUUCDHAZGAVEZ-UHFFFAOYSA-N

Related Categories

Application

3-(Trimethylsilyl)-1-propanol has been used in:
  • the synthesis of telechelic oligomers via atom transfer radical polymerization (ATRP) of styrene
  • the preparation of the β-seleno-γ-silyl alcohols

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Silicon-controlled rearrangement versus Krief-Reich reaction in ?-seleno-?-silyl alcohols: a new stereoselective synthesis of terminally-substituted allylsilanes.
Sarkar TK and Ghosh SK.
Tetrahedron Letters, 28(18), 2061-2064 (1987)
Synthesis of Telechelic Oligomers via Atom Transfer Radical Polymerization, 1.
Otazaghine B, et al.
Macromolecular Chemistry and Physics, 205(2), 154-164 (2004)
Adam Czajka et al.
Physical chemistry chemical physics : PCCP, 19(35), 23869-23877 (2017-07-21)
Presented here are the results for a novel class of hydrocarbon surfactants, termed trimethylsilyl hedgehogs (TMS-hedgehogs), due to the presence of silicon in the tails. By comparing the surface properties of these hybrid hedgehogs to purely hydrocarbon equivalents, links between

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