Lithium Borohydride

For research use only. Not for therapeutic Use.

  • CAT Number: R045177
  • CAS Number: 16949-15-8
  • Molecular Formula: BLi
  • Molecular Weight: 17.75
  • Purity: ≥95%
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<p>
<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">Lithium Borohydride (CAS 16949-15-8)<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;is a tetrahydroborate</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;and known in organic synthesis as &nbsp;in a reducing agent for esters.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;Although less common than the related sodium borohydride,</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;the lithium salt offers some advantages, being a stronger reducing agent and highly soluble in ethers, whilst remaining safer to handle than&nbsp;</span><span style="caret-color: rgb(32, 33, 34); orphans: 2; widows: 2;">lithium aluminium hydride.&nbsp;</span></span></span></span></p>


Catalog Number R045177
CAS Number 16949-15-8
Synonyms

Lithium Tetrahydroborate (1:1); Lithium Boron Hydride; Lithium Hydroborate (LiBH4); Lithium Tetrahydroborate

Molecular Formula BLi
Purity ≥95%
Storage -20°C
IUPAC Name lithium;boron(1-)
InChI InChI=1S/B.Li/q-1;+1
InChIKey NZTNZPDOBQDOSO-UHFFFAOYSA-N
SMILES [Li+].[B-]
Reference

<p>
<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">1.<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Banfi, Luca, et al. &quot;Lithium Borohydride.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Encyclopedia of Reagents for Organic Synthesis</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;(2001).<br />
2.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Soai, Kenso, and Atsuhiro Ookawa. &quot;Mixed solvents containing methanol as useful reaction media for unique chemoselective reductions within lithium borohydride.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">The Journal of Organic Chemistry</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;51.21 (1986): 4000-4005.<br />
3.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Schlesinger, H. I., and Herbert C. Brown. &quot;Metallo borohydrides. III. Lithium borohydride.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Journal of the American Chemical Society</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;62.12 (1940): 3429-3435.</span></span></span></span></p>

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