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Merck
CN

8.06373

Sodium borohydride

fine granular for synthesis

别名:

Sodium borohydride, Sodium tetrahydridoborate

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关于此项目

经验公式(希尔记法):
H4BNa
化学文摘社编号:
分子量:
37.83
UNSPSC Code:
12352306
EC Index Number:
241-004-4
NACRES:
NA.22
MDL number:
Form:
solid
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vapor pressure

<1 hPa ( 25 °C)

Quality Level

form

solid

autoignition temp.

220 °C

potency

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

expl. lim.

3.02 % (v/v)

reaction suitability

reagent type: reductant

pH

11 (20 °C, 10 g/L in H2O)

bp

500 °C (decomposition)

mp

>360 °C (slow decomposition)

transition temp

flash point 69 °C

density

1.07 g/cm3 at 20 °C

bulk density

350‑500 kg/m3

storage temp.

2-30°C

SMILES string

[Na+].[B-H2]

InChI

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

InChI key

YOQDYZUWIQVZSF-UHFFFAOYSA-N

General description

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.

Application

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.

Analysis Note

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


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Danger

supp_hazards

flash_point_f

Not applicable

flash_point_c

Not applicable

Hazard Classifications

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

存储类别

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

法规信息

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实验方案

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.





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