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8.06373
Sodium borohydride
fine granular for synthesis
Recommended Products
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
InChI
1S/BH4.Na/h1H4;/q-1;+1
InChI key
YOQDYZUWIQVZSF-UHFFFAOYSA-N
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This Item | 8.18823 | 71320 | 247677 |
|---|---|---|---|
| reaction suitability reagent type: reductant | reaction suitability reagent type: reductant | reaction suitability reagent type: reductant | reaction suitability reagent type: reductant |
| bp 500 °C (decomposition) | bp 500 °C (decomposition) | bp - | bp - |
| mp >360 °C (slow decomposition) | mp >360 °C (slow decomposition) | mp >300 °C (dec.) (lit.) | mp >300 °C (dec.) (lit.) |
| density 1.07 g/cm3 at 20 °C | density 1.07 g/cm3 at 20 °C | density - | density - |
| storage temp. 2-30°C | storage temp. 2-30°C | storage temp. - | storage temp. - |
General description
Application
- 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
Identity (ICP-OES): passes test
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Eye Dam. 1 - Repr. 1B - Skin Corr. 1B - Water-react 1
Supplementary Hazards
Storage Class Code
4.3 - Hazardous materials, which set free flammable gases upon contact with water
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Protocols
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.
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