Lithium triethylborohydride

Lithium triethylborohydride
Skeletal formula of lithium triethylborohydride
Names
Preferred IUPAC name
Lithium triethylboranuide
Other names
Superhydride
LiTEBH
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.040.963 Edit this at Wikidata
EC Number
  • 245-076-8
UNII
  • InChI=1S/C6H16B.Li/c1-4-7(5-2)6-3;/h7H,4-6H2,1-3H3;/q-1;+1 checkY
    Key: WCJAYABJWDIZAJ-UHFFFAOYSA-N checkY
  • [Li+].CC[BH-](CC)CC
Properties
Li(C2H5)3BH
Molar mass 105.95 g/mol
Appearance Colorless to yellow liquid
Density 0.890 g/cm3, liquid
Boiling point 66 °C (151 °F; 339 K) for THF
reactive
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
highly flammable
corrosive
Causes burns
Probable Carcinogen
GHS labelling:[1]
GHS02: FlammableGHS05: CorrosiveGHS07: Exclamation mark
Danger
H250, H260, H314, H335
P210, P222, P223, P231+P232, P260, P261, P264, P271, P280, P301+P330+P331, P302+P334, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P335+P334, P363, P370+P378, P402+P404, P403+P233, P405, P422, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasFlammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuelInstability 2: Undergoes violent chemical change at elevated temperatures and pressures, reacts violently with water, or may form explosive mixtures with water. E.g. white phosphorusSpecial hazard W: Reacts with water in an unusual or dangerous manner. E.g. sodium, sulfuric acid
3
2
2
Safety data sheet (SDS) External MSDS
Related compounds
Related hydride
Lithium borohydride
sodium borohydride
sodium hydride
lithium aluminium hydride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Lithium triethylborohydride is the organoboron compound with the formula LiEt3BH. Commonly referred to as LiTEBH or Superhydride, it is a powerful reducing agent used in organometallic and organic chemistry. It is a colorless or white liquid but is typically marketed and used as a THF solution.[2] The related reducing agent sodium triethylborohydride is commercially available as toluene solutions.

LiBHEt3 is a stronger reducing agent than lithium borohydride and lithium aluminium hydride.

  1. ^ "Lithium triethylhydroborate". pubchem.ncbi.nlm.nih.gov. Retrieved 19 December 2021.
  2. ^ Zaidlewicz, M.; Brown, H.C. (2001). "Lithium Triethylborohydride". Encyclopedia of Reagents for Organic Synthesis. John Wiley & Sons. doi:10.1002/047084289X.rl148. ISBN 0471936235. Retrieved 2022-02-18.