跳转至内容
Merck
所有图片(1)

Key Documents

8.06373

Sigma-Aldrich

Sodium borohydride

fine granular for synthesis

别名:

Sodium borohydride, Sodium tetrahydridoborate

登录查看公司和协议定价


About This Item

经验公式(希尔记法):
H4BNa
CAS号:
分子量:
37.83
MDL號碼:
分類程式碼代碼:
12352306
酶委員會索引編號:
241-004-4
NACRES:
NA.22

蒸汽壓力

<1 hPa ( 25 °C)

品質等級

形狀

solid

自燃溫度

220 °C

效力

160 mg/kg LD50, oral (Rat)
230 mg/kg LD50, skin (Rabbit)

expl. lim.

3.02 % (v/v)

反應適用性

reagent type: reductant

pH值

11 (20 °C, 10 g/L in H2O)

bp

500 °C (decomposition)

mp

>360 °C (slow decomposition)

轉變溫度

flash point 69 °C

密度

1.07 g/cm3 at 20 °C

體積密度

350‑500 kg/m3

儲存溫度

2-30°C

InChI

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

InChI 密鑰

YOQDYZUWIQVZSF-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

一般說明

Sodium borohydride (NaBH4) is the most commonly available borohydride used in several industrial applications. It is considered as a selective reducing agent due to its ability to selectively reduce aldehydes and ketones into their corresponding alcohols in the presence of other functional groups such as nitro, ester, amide, lactone, epoxide, and nitriles. Ethanol and methanol are usually employed as solvents in NaBH4 reduction reactions.

應用

Sodium borohydride (fine granular) can be used as a reducing agent to prepare:
  • Zero valent iron nanoparticles supported on mesoporous carbon (Starbon) by in situ reductions of Fe3+ ions.
  • Ag nanoparticles on graphene using AgNO3 as a precursor.
  • Ag-Pd/ZrO2 catalytic system applicable in plasmonic catalysis. It can also be used as a source to store as well as generate hydrogen for energy-carrier applications.

分析報告

Assay (hypochlorite): ≥ 98.0 %
Identity (ICP-OES): passes test

訊號詞

Danger

危險分類

Acute Tox. 3 Oral - Eye Dam. 1 - Repr. 1B - Skin Corr. 1B - Water-react 1

安全危害

儲存類別代碼

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

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Sodium Borohydride
Banfi Luca, et al.
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2014)

相关内容

Fmoc resin cleavage and deprotection follows the difficult task of detaching the peptide from the resin support and removing all the side-chain protecting groups of the amino acid residues to yield the desired peptide.

Fmoc resin cleavage and deprotection follows the difficult task of detaching the peptide from the resin support and removing all the side-chain protecting groups of the amino acid residues to yield the desired peptide.

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门