Silane

Silane
Names
IUPAC name
Silane
Systematic IUPAC name
Silicane
Other names
  • Monosilane
  • Silicon(IV) hydride
  • Silicon tetrahydride
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.029.331
Gmelin Reference
273
RTECS number
  • VV1400000
UNII
UN number 2203
CompTox Dashboard (EPA)
  • InChI=1S/SiH4/h1H4 Y
    Key: BLRPTPMANUNPDV-UHFFFAOYSA-N Y
  • InChI=1/SiH4/h1H4
    Key: BLRPTPMANUNPDV-UHFFFAOYAE
SMILES
  • [SiH4]
Properties
H4Si
Molar mass 32.117 g·mol−1
Appearance Colorless gas
Odor Repulsive[1]
Density 1.313 g/L[2]
Melting point −185 °C (−301.0 °F; 88.1 K)[2]
Boiling point −111.9 °C (−169.4 °F; 161.2 K)[2]
Reacts slowly[2]
Vapor pressure >1 atm (20 °C)[1]
Conjugate acid Silanium (sometimes spelled silonium)
Structure
Molecular shape
Tetrahedral
r(Si-H) = 1.4798 Å[3]
Dipole moment
0 D
Thermochemistry[4]
42.81 J/mol·K
Std molar
entropy (S298)
204.61 J/mol·K
34.31 kJ/mol
56.91 kJ/mol
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Extremely flammable, pyrophoric in air
GHS labelling:
Pictograms
Danger
Hazard statements
H220 [5]
Precautionary statements
P210, P222, P230, P280, P377, P381, P403, P410+P403
NFPA 704 (fire diamond)
1
4
3
Flash point Not applicable, pyrophoric gas
Autoignition
temperature
~ 18 °C (64 °F; 291 K)
Explosive limits 1.37–100%
NIOSH (US health exposure limits):
PEL (Permissible)
None[1]
REL (Recommended)
TWA 5 ppm (7 mg/m3)[1]
IDLH (Immediate danger)
N.D.[1]
Safety data sheet (SDS) ICSC 0564
Related compounds
Related tetrahydride compounds
Methane
Germane
Stannane
Plumbane
Related compounds
Phenylsilane
Vinylsilane
Disilane
Trisilane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Silane (Silicane) is an inorganic compound with chemical formula SiH4. It is a colorless, pyrophoric gas with a sharp, repulsive, pungent smell, somewhat similar to that of acetic acid.[6] Silane is of practical interest as a precursor to elemental silicon. Silanes with alkyl groups are effective water repellents for mineral surfaces such as concrete and masonry. Silanes with both organic and inorganic attachments are used as coupling agents. They are commonly used to apply coatings to surfaces or as an adhesion promoter.[7]

  1. ^ a b c d e NIOSH Pocket Guide to Chemical Hazards. "#0556". National Institute for Occupational Safety and Health (NIOSH).
  2. ^ a b c d Haynes, p. 4.87
  3. ^ Haynes, p. 9.29
  4. ^ Haynes, p. 5.14
  5. ^ Linde Safety Data Sheet
  6. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. doi:10.1016/C2009-0-30414-6. ISBN 978-0-08-037941-8.
  7. ^ London, Gábor; Carroll, Gregory T.; Feringa, Ben L. (2013). "Silanization of quartz, silicon and mica surfaces with light-driven molecular motors: construction of surface-bound photo-active nanolayers". Organic & Biomolecular Chemistry. 11 (21): 3477–3483. doi:10.1039/c3ob40276b. ISSN 1477-0520. PMID 23592007. S2CID 33920329.