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Lithium Triethylborohydride

CAS No.
22560-16-3
Chemical Name:
Lithium Triethylborohydride
Synonyms
SUPER-HYDRIDE;LITHIUM TRIETHYLHYDROBORATE;ithium triethyL;SUPER-HYDRIDE(R);super-hydride solution;LITHIUM TRIETHYLHYDROBOR;Lithiumtriethylhydroborat;Super-Hydride(R) solution;LITHIUM TRIETHYLBOROHYDRIDE;Lithium borohydride thiethyl
CBNumber:
CB7758452
Molecular Formula:
C6H13BLi
Molecular Weight:
102.92
MDL Number:
MFCD00011703
MOL File:
22560-16-3.mol
Last updated:2023-04-23 13:52:06

Lithium Triethylborohydride Properties

Melting point 66-67° (Binger); mp 78-83° (dec) (Brown, 1977)
Density 0.892 g/mL at 25 °C
Flash point 1 °F
storage temp. Flammables + water-Freezer (-20°C)e area
solubility Miscible with tetrahydrofuran and benzene.
form Liquid
color Colorless to light gray
Sensitive Air & Moisture Sensitive
Merck 14,5544
BRN 4151240
Exposure limits ACGIH: TWA 50 ppm; STEL 100 ppm (Skin)
OSHA: TWA 200 ppm(590 mg/m3)
NIOSH: IDLH 2000 ppm; TWA 200 ppm(590 mg/m3); STEL 250 ppm(735 mg/m3)
CAS DataBase Reference 22560-16-3(CAS DataBase Reference)
FDA UNII Q1ML638JFD

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS02,GHS05,GHS07,GHS08
Signal word  Danger
Hazard statements  H318-H333-H225-H260-H302-H314-H335-H351
Precautionary statements  P210-P231+P232-P280-P370+P378-P402+P404-P403+P235-P223-P303+P361+P353-P305+P351+P338-P405-P501a
Hazard Codes  F,C
Risk Statements  11-14/15-19-34-40-37
Safety Statements  16-26-33-36/37/39-43-45
RIDADR  UN 3399 4.3/PG 1
WGK Germany  1
10-23
HazardClass  4.3
PackingGroup  I
HS Code  29319090
NFPA 704
4
3 2
W

Lithium Triethylborohydride price More Price(20)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 179728 Super-Hydride® solution 1.0?M lithium triethylborohydride in THF 22560-16-3 4X25ML $152 2024-03-01 Buy
Sigma-Aldrich 179728 Super-Hydride? solution 1.0 M lithium triethylborohydride in THF 22560-16-3 8l $820 2024-03-01 Buy
Sigma-Aldrich 179728 Super-Hydride? solution 1.0 M lithium triethylborohydride in THF 22560-16-3 2l $874 2023-06-20 Buy
TCI Chemical L0190 Lithium Triethylborohydride (ca. 12% in Tetrahydrofuran, ca. 1.0mol/L) 22560-16-3 100mL $131 2021-12-16 Buy
TCI Chemical L0190 Lithium Triethylborohydride (ca. 12% in Tetrahydrofuran, ca. 1.0mol/L) 22560-16-3 500mL $458 2021-12-16 Buy
Product number Packaging Price Buy
179728 4X25ML $152 Buy
179728 8l $820 Buy
179728 2l $874 Buy
L0190 100mL $131 Buy
L0190 500mL $458 Buy

Lithium Triethylborohydride Chemical Properties,Uses,Production

Description

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. 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.

Chemical Properties

colorless to light grey cloudy solution

Uses

LiTEBH can be used as a reagent:

  • To reduce alkyl halides to alkanes via dehydrogenation reactions.
  • For the selective reduction of epoxides to Markovnikov alcohols.
  • To reduce tosylates or mesylates primary alcohols to hydrocarbons.
  • For reductive cyclization reactions for the preparation of useful intermediates.
  • In the synthesis of hepta(manno-3-deoxy-6-O-t-butyldimethylsilyl)-β-cyclodextrin by reduction of hepta(manno-2,3-anhydro-6-O-t-butyldimethylsilyl)-β-cyclodextrin.
  • For hydrodefluorination of C-F bonds using Ni catalyst.
  • To prepare alkynyl alcohols from cleavage of cyclic keto-vinyl triflates.
  • In the stereoselective reduction of bicyclic imides, isoquinolines, and pyridines.
  • To prepare tungsten and molybdenum hydride complexes.

Uses

Powerful and selective reducing agent.
As a reducing agentLithium triethylborohydride is used as a powerful reducing agent in organic synthesis for the conversion of carbonyl compounds to alcohols. It is also used in the preparation of alkynyl alcohols from the cleavage of cyclic keto-vinyl triflates. It is also used in the reduction of esters and lactones to alcohol and diol respectively. Further, it is used to prepare 1-methylcyclohexanol and 1,4-butanediol from 1,2-epoxybutane and gamma-butyrolactone respectively. It is also utilized for reductive cleavage of mesylates and tosylates in synthetic organic chemistry.

Preparation

LiBHEt3 is prepared by the reaction of lithium hydride (LiH) and triethylborane (Et3B) in tetrahydrofuran (THF):
LiH + Et3B → LiEt3BH
Its THF solutions are stable indefinitely in the absence of moisture and air.

Application

Lithium Triethylborohydride (LiTEBH) is widely used as a powerful and selective reducing agent that shows super hydride activity in organic synthesis.
LiTEBH can be used as a reagent:
To reduce alkyl halides to alkanes via dehydrogenation reactions.
For the selective reduction of epoxides to Markovnikov alcohols.
To reduce tosylates or mesylates primary alcohols to hydrocarbons.
For reductive cyclization reactions for the preparation of useful intermediates.
In the synthesis of hepta(manno-3-deoxy-6-O-t-butyldimethylsilyl)-β-cyclodextrin by reduction of hepta(manno-2,3-anhydro-6-O-t-butyldimethylsilyl)-β-cyclodextrin.
For hydrodefluorination of C-F bonds using Ni catalyst.
To prepare alkynyl alcohols from cleavage of cyclic keto-vinyl triflates.
In the stereoselective reduction of bicyclic imides, isoquinolines, and pyridines.
To prepare tungsten and molybdenum hydride complexes.

General Description

Super-Hydride? solution (Lithium triethylborohydride or LiTEBH) is widely used as a powerful and selective reducing agent that shows super hydride activity in organic synthesis.

Precautions

Moisture sensitive. Air sensitive. Incompatible with water and strong oxidizing agents.

References

Tamang, S.; Kim, K.; Choi, H.; Kim, Y.; Jeong, S. Synthesis of colloidal InSb nanocrystals via in situ activation of InCl3. Dalton Trans. 2015, 44 (38), 16923-16928.
Kandapallil, B.; Colborn, R. E.; Bonitatibus, P. J.; Johnson, F. Synthesis of high magnetization Fe and FeCo nanoparticles by high temperature chemical reduction. J. Magn. Magn. Mater. 2015, 378, 535-538.

Lithium Triethylborohydride Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 202)Suppliers
Supplier Tel Email Country ProdList Advantage
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21634 55
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28172 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49374 58
career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29811 58
Antai Fine Chemical Technology Co.,Limited
18503026267 info@antaichem.com CHINA 9636 58
SIMAGCHEM CORP
+86-13806087780 sale@simagchem.com China 17365 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +8618949823763 sales@tnjchem.com China 34563 58
ANHUI WITOP BIOTECH CO., LTD
+8615255079626 eric@witopchemical.com China 23541 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 7724 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com China 52849 58

View Lastest Price from Lithium Triethylborohydride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Lithium Triethylborohydride pictures 2023-03-11 Lithium Triethylborohydride
22560-16-3
US $0.00 / kg 1kg 98.0%min 1000kg LY Global chemicals co.,ltd .
		LITHIUM TRIETHYLBOROHYDRIDE pictures 2020-01-10 LITHIUM TRIETHYLBOROHYDRIDE
22560-16-3
US $1.00 / KG 1g 98% 200kgs Career Henan Chemical Co

Lithium Triethylborohydride Spectrum

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