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Sulfamic acid
Sulfamic Acid
Application Notes
Sulfamic acid (H2NSO3H) may be used in the following studies:• As catalyst in the synthesis of aryl-14H-dibenzo[a.j]xanthenes.• As green catalyst for the preparation of amide from ketoxime.• As ammonia equivalent in the regioselective synthesis of primary allylic amines, via allylic substitution reactions.• Synthesis of polysubstituted quinolones.Sulfamic acid may be used in the following processes:• As a titrant in the determination of the burette injection volume and chemical calibration factor.• To neutralize excess nitrous acid in the colorimetric paracetamol assay by modified Glynn and Kendal colorimetric method.• To prevent endogenous mercury (Hg) loss during the urine Hg measurement by inductively coupled plasma mass spectrometry (ICP-MS) method.• As an acid catalyst and a hypochlorite scavenger in the chlorite oxidation of dialdehyde cellulose (DAC).• As a heterogeneous catalyst in the synthesis of polyhydroquinoline derivatives by Hantzsch condensation reaction.• As catalyst in the degradation of bamboo fiber to 5-hydroxymethylfurfural (HMF).• As an acid reagent in the determination of silicates in water samples based on centrifugal microfluidics.• As catalyst in the synthesis of deazaoxaflavin at room temperature.
Usage Statement
Unless specified otherwise, MP Biomedical's products are for research or further manufacturing use only, not for direct human use. For more information, please contact our customer service department.
Key Applications
Catalyst
SKU | 02194860-CF |
Alternate Names | Amidosulfonic acid |
Application Notes | Sulfamic acid (H2NSO3H) may be used in the following studies:• As catalyst in the synthesis of aryl-14H-dibenzo[a.j]xanthenes.• As green catalyst for the preparation of amide from ketoxime.• As ammonia equivalent in the regioselective synthesis of primary allylic amines, via allylic substitution reactions.• Synthesis of polysubstituted quinolones.Sulfamic acid may be used in the following processes:• As a titrant in the determination of the burette injection volume and chemical calibration factor.• To neutralize excess nitrous acid in the colorimetric paracetamol assay by modified Glynn and Kendal colorimetric method.• To prevent endogenous mercury (Hg) loss during the urine Hg measurement by inductively coupled plasma mass spectrometry (ICP-MS) method.• As an acid catalyst and a hypochlorite scavenger in the chlorite oxidation of dialdehyde cellulose (DAC).• As a heterogeneous catalyst in the synthesis of polyhydroquinoline derivatives by Hantzsch condensation reaction.• As catalyst in the degradation of bamboo fiber to 5-hydroxymethylfurfural (HMF).• As an acid reagent in the determination of silicates in water samples based on centrifugal microfluidics.• As catalyst in the synthesis of deazaoxaflavin at room temperature. |
Base Catalog Number | 194860 |
CAS # | 5329-14-6 |
Density | 2.15 |
EC Number | 226-218-8 |
Format | Crystalline powder |
Grade | ACS grade |
Hazard Statements | H315-H319-H412 |
Insoluble Matter | <0.01% |
Melting Point | 205 DEG C |
Molecular Formula | NH2SO3H |
Molecular Weight | 97.088 g/mol |
Personal Protective Equipment | Dust mask , Eyeshields, Gloves |
pH | 1N, pH=0.41; 0.75N, pH=0.5; 0.5N, pH=0.63; 0.25N, pH=0.87; 0.1N, pH=1.18; 0.05N, pH=1.41; 0.01N, pH=2.02 |
RTECS Number | WO5950000 |
Safety Symbol | GHS07 |
Solubility | SPARINGLY SOL IN ALC, <a class="pubchem-internal-link CID-887" href="https://pubchem.ncbi.nlm.nih.gov/compound/METHANOL">METHANOL</a>; SLIGHTLY SOL IN <a class="pubchem-internal-link CID-180" href="https://pubchem.ncbi.nlm.nih.gov/compound/ACETONE">ACETONE</a>; INSOL IN ETHER; FREELY SOL IN NITROGENOUS BASES AND IN <a class="pubchem-internal-link CID-947" href="https://pubchem.ncbi.nlm.nih.gov/compound/NITROGEN">NITROGEN</a> CONTAINING ORG SOLVENTS |
Usage Statement | Unless specified otherwise, MP Biomedical's products are for research or further manufacturing use only, not for direct human use. For more information, please contact our customer service department. |