Sulfamic acid - Reagent Grade, High-purity, ≥99% , CAS No.5329-14-6

CAS: 5329-14-6 Cat. No.: S432841 Summenformel: H3NO3S Molekulargewicht: 97.09 EG-Nummer: 226-218-8
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QUALITÄT & REINHEIT Reagent Grade ? General reagent-grade purity suitable for most laboratory work. Use as a dependable default when no specific higher grade is required. High-purity ? High-purity grade with substantially reduced impurity levels. Use when trace contaminants would interfere with your measurement or process. ≥99%
Synonyms
SULFAMIC ACID [MI]|SULFAMIC ACID, ACS|Sulfamic acid [UN2967] [Corrosive]|Kyselina amidosulfonova|Sulphamic-acid-|AMINESULFONIC ACID|Kyselina sulfaminova|Amidosulfuric acid|Imidosulfonic acid|SULFAMIC ACID, REAG|Aminosulfonic acid|amidohydroxidodioxidosulfur|Amidoschwefelsaeure|Jumbo|Sulphamic acid|ALPROJET W|Amidosulfonic acid|Aminosulfuric acid|Sulfaminic acid|sulfuramidic acid|amidosulphuric acid|Sulphamidic acid|Kyselina sulfaminova [Czech]|SCALE CLEEN|SULFAMIC ACID|Sulfamidsaeure|Sulfamic acid [UN2967] [Corrosive]
Storage
Room temperature
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5g
S432841-5g
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100g
S432841-100g
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S432841-500g
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Übersicht

Gene Information

human ... CA1(759), CA2(760)


General Description

Sulfamic acid (H 2 NSO 3 H) is a strong inorganic acid. It exists in zwitterionic form and neutral forms. Zwitterionic form is more stable than neutral form. The ability of sulfamic acid/zinc powder to reduce nitrate to nitrogen gas under acidic condition has been utilized to denitrify nitrate-rich wastewater.


Application

Sulfamic acid (H 2 NSO 3 H) may be used in the following studies: As a catalyst in the synthesis of aryl-14 H -dibenzo[ a . j ]xanthenes. As a green catalyst for the liquid Beckmann rearrangement of ketoxime in dried acetonitrile. As a nitrogen source as well as an in situ activator of hydroxy groups in the direct iridium-catalyzed synthesis of primary allylic amines from allylic alcohols. Synthesis of polysubstituted quinolones.

Spezifikationen

Synonyme
SULFAMIC ACID [MI] | SULFAMIC ACID, ACS | Sulfamic acid [UN2967] [Corrosive] | Kyselina amidosulfonova | Sulphamic-acid- | AMINESULFONIC ACID | Kyselina sulfaminova | Amidosulfuric acid | Imidosulfonic acid | SULFAMIC ACID, REAG | Aminosulfonic acid | amidohydroxidodioxidosulfur | Amidoschwefelsaeure | Jumbo | Sulphamic acid | ALPROJET W Show more
Spezifikationen & Reinheit
Reagent Grade, High-purity, ≥99%
Storage
Room temperature
Verschickt in
FedEx DG Service
Note
High-purity, Reagent Grade
Reinheit
≥99%
Namen und Kennungen
Pubchem Sid
Kanonisches Lächeln
NS(=O)(=O)O
IUPAC Name
sulfamic acid
InChIKey
IIACRCGMVDHOTQ-UHFFFAOYSA-N
INCHI
1S/H3NO3S/c1-5(2,3)4/h(H3,1,2,3,4)
Isomere SMILES
NS(=O)(=O)O
WGK Deutschland
1
UN-Nummer
2967
Verpackungsgruppe
III
Molekulargewicht
97.09
Reaxy-Rn
3043314
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3043314&ln=

Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

KingdomInorganic compounds
SuperclassHomogeneous non-metal compounds
KlasseOther non-metal organides
SubclassOther non-metal oxides
Intermediate Tree Nodes Not available
Direct ParentOther non-metal oxides
Alternative Parents Sulfuric acid monoamides  Inorganic oxides  
Molecular FrameworkNot available
Substituents Other non-metal oxide - Sulfuric acid monoamide - Inorganic oxide
BeschreibungThis compound belongs to the class of inorganic compounds known as other non-metal oxides. These are inorganic compounds containing an oxygen atom of an oxidation state of -2, in which the heaviest atom bonded to the oxygen belongs to the class of 'other non-metals'.
External Descriptors sulfamic acids
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CXCL8 Tchem Interleukin-8 (642 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA6 Tclin Carbonic anhydrase VI (993 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GBA1 Tclin Beta-glucocerebrosidase (14647 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5B Tclin Carbonic anhydrase VB (957 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5A Tclin Carbonic anhydrase VA (1168 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA14 Tclin Carbonic anhydrase XIV (1305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA12 Tclin Carbonic anhydrase XII (6231 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA9 Tclin Carbonic anhydrase IX (8255 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H157 (619 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HCEC (18 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NT5E Tchem 5'-nucleotidase (622 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Zugehörige Ziele (nicht menschlich)
Ca7 Carbonic anhydrase VII (3 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca13 Carbonic anhydrase XIII (322 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA4 Carbonic anhydrase IV (1713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Carbonic anhydrase (69 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trypanosoma cruzi (99888 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA Alpha carbonic anhydrase (93 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot NumberCertificate TypeDatumArtikel
D23081636D23081636Certificate of AnalysisMar 28, 2023 S432841
D23081640D23081640Certificate of AnalysisMar 28, 2023 S432841
D23081681D23081681Certificate of AnalysisMar 28, 2023 S432841
D23081682D23081682Certificate of AnalysisMar 28, 2023 S432841
D23081686D23081686Certificate of AnalysisMar 28, 2023 S432841
Chemische und physikalische Eigenschaften
Löslichkeitwater: 50mg/mL, clear, colorless
Schmelzpunkt (°C)205°C
Molekulargewicht97.100 g/mol
XLogP3-1.600
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count0
Exact Mass96.9834 Da
Monoisotopic Mass96.9834 Da
Topological Polar Surface Area88.800 Ų
Heavy Atom Count5
Formal Charge0
Complexity92.600
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
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Citations of This Product
Lösungsrechner
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