Merck
CN

230200

Sigma-Aldrich

硼氢化锂 溶液

2.0 M in THF

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别名:
Lithium boron hydride, Lithium hydroborate
线性分子式:
LiBH4
CAS号:
分子量:
21.78
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

形式

liquid

质量水平

反应适用性

reagent type: reductant

浓度

2.0 M in THF

密度

0.896 g/mL at 25 °C

SMILES字符串

[Li+].[H][B-]([H])([H])[H]

InChI

1S/BH4.Li/h1H4;/q-1;+1

InChI key

UUKMSDRCXNLYOO-UHFFFAOYSA-N

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相关类别

应用

反应物用于:
  • 镓、铟、铼和锌三(巯基咪唑基)氢硼酸配合物的制备
  • 机械化学复分解反应
  • 非催化水解制氢
  • 大型金单层保护簇的生长
  • 阴离子取代反应
  • 脱氢反应
硼氢化锂溶液 (2M in THF) 分别用于 5-亚苄基-2,4-噻唑烷二酮类和 5-亚苄基-4-氧代-2-噻唑烷二酮类的还原,并分别生成 5-苄基-2,4-噻唑烷二酮类和 5-苄基-4-氧代-2-噻唑烷二酮类。

包装

推荐将25毫升安全/密封瓶作为一次性使用的瓶子。重复穿刺可能会导致产品性能下降。

法律信息

Sure/Seal is a trademark of Sigma-Aldrich Co. LLC

警示用语:

Danger

危险分类

Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - Water-react 1

补充剂危害

储存分类代码

4.3 - Hazardous materials, which set free flammable gases upon contact with water

WGK

WGK 2

闪点(°F)

-0.4 °F - closed cup

闪点(°C)

-18 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

易制爆化学品
危险化学品

分析证书(COA)

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示例

T1503
货号
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包装规格/数量

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1000309185

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索取COA

  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

  2. How do I get lot-specific information or a Certificate of Analysis?

    The lot specific COA document can be found by entering the lot number above under the "Documents" section.

  3. Why does Product 230200, Lithium Borohydride, need to be handled under nitrogen?

    This product is moisture sensitive, reacting violently with water, liberating extremely flammable gases.

  4. Is the tetrahydrofuran (THF) used in Product 230200, Lithium Borohydride, stabilized?

    The THF used in this product is stabilized with 0.025% butylated hydroxytoluene (BHT).

  5.  Is it necessary to refrigerate Product 230200, Lithium Borohydride?

    We do recommend to refrigerate this product, since it may develop pressure at room temperature.

  6. What types of reactions is Product 230200, Lithium Borohydride, used in?

    It is reagent for reduction of compounds containing ketonic, aldehydic, or ester carbonyls and a nitrile group, where reduction of the carbonyl but not of the nitrile group is wanted.

  7. Is Product 230200, Lithium Borohydride, an energy carrier?

    Lithium borohydride is renowned for one of the highest energy density chemical energy carriers.  By reacting with atmospheric oxygen, it liberates large amounts of heat. 

  8. How do I find price and availability?

    There are several ways to find pricing and availability for our products. Once you log onto our website, you will find the price and availability displayed on the product detail page. You can contact any of our Customer Sales and Service offices to receive a quote.  USA customers:  1-800-325-3010 or view local office numbers.

  9. What is the Department of Transportation shipping information for this product?

    Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product. 

  10. My question is not addressed here, how can I contact Technical Service for assistance?

    Ask a Scientist here.

Regiospecific reduction of 5-benzylidene-2, 4-thiazolidinediones and 4-oxo-2-thiazolidinethiones using lithium borohydride in pyridine and tetrahydrofuran.
Giles RG
Tetrahedron, 56(26), 4531-4537 (2000)
Hui Wu et al.
Nanotechnology, 20(20), 204002-204002 (2009-05-08)
The use of Li3BN2H8 complex hydride as a practical hydrogen storage material is limited by its high desorption temperature and poor reversibility. While certain catalysts have been shown to decrease the dehydrogenation temperature, no significant improvement in reversibility has been
Mark R Biscoe et al.
Journal of the American Chemical Society, 125(42), 12718-12719 (2003-10-16)
Three hydrophobic borohydrides carrying phenyl, pentafluorophenyl, and beta-naphthyl groups were used to reduce ketones in water and in methanol. With ketones carrying phenyl, naphthyl, or biphenyl substituents, there was preferential reduction in methanol of competing acetyl groups, either intermolecular or
[New method of cleaving the N-linked carbohydrate chains of glycoproteins using alkaline lithium borohydride].
L M Likhosherstov et al.
Doklady Akademii nauk SSSR, 274(1), 222-225 (1984-01-01)
S M Opalka et al.
Nanotechnology, 20(20), 204024-204024 (2009-05-08)
Experimentation, thermodynamic modeling, and atomic modeling were combined to screen the reactivity of SiO2, Al2O3, and ZrO2 nanoscale oxides with LiBH4. Equilibrium thermodynamic modeling showed that the reactions of oxides with LiBH4 could lead to formation of stable Li-bearing oxide

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