Merck
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A6141

Sigma-Aldrich

Ammonium bicarbonate

ReagentPlus®, ≥99.0%

Synonym(s):
Ammonium hydrogen carbonate
Linear Formula:
NH4HCO3
CAS Number:
Molecular Weight:
79.06
Beilstein:
4329606
EC Number:
MDL number:
eCl@ss:
38020216
PubChem Substance ID:
NACRES:
NA.21

Quality Level

vapor density

2.7 (vs air)

vapor pressure

513 hPa ( 50 °C)
67.1 hPa ( 20 °C)

product line

ReagentPlus®

assay

≥99.0%

form

powder or crystals

pH

7-8.5 (25 °C, 79.1 g/L)

SMILES string

N.OC(O)=O

InChI

1S/CH2O3.H3N/c2-1(3)4;/h(H2,2,3,4);1H3

InChI key

ATRRKUHOCOJYRX-UHFFFAOYSA-N

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General description

Ammonium bicarbonate is an inorganic salt commonly used in the food industry. It can be generated by the interaction of gaseous carbon dioxide and aqueous ammonia. The addition of ammonium bicarbonate to microbial fuel cells (MFCs) has been reported to improve its functioning by altering the porosity and pore distribution of catalyst layers. A recent study reports the use of bubble column evaporator (BCE) based analysis of its thermal degradation in aqueous solution.

Application

Ammonium bicarbonate (AMBIC) was used in the following studies:
  • To derivatize histone proteins from human monocyte-derived macrophages (MDM) by propionylation.
  • Destaining of silver-stained proteins in polyacrylamide gel bands during the peptide mass profiling using a mass spectrometer.
  • Digestion of proteins isolated from Xenopus egg extracts in coomassie blue-stained gel bands during the analysis of microtubule-binding proteins.

Packaging

25, 500 g in poly bottle
1 kg in poly bottle

Legal Information

ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Certificate of Analysis

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Certificate of Origin

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Product Information Sheet

More Documents

Quotes and Ordering

Protocols

Protocols for the Fmoc SPPS of Cysteine-containing Peptides

Overcome challenges in synthesis and disulfide bond formation with protocols for Fmoc solid-phase peptide synthesis of peptides with cysteine and methionine.

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