Chloramine-T - ≥95% , CAS No.149358-73-6

CAS: 149358-73-6 Cat. No.: C353516 Formula: CH₃C₆H₄SO₂N(Cl)Na·xH₂O Peso molecolare: 227.64 (anhydrous basis) Numero EC: 682-756-7 PubChem CID: 16218604

GRADE & PURITY ≥95%

Synonyms

SCHEMBL2441113 | Sodium chloro(tosyl)amide xhydrate | Sodium chloro(tosyl)amide hydrate | Chloramine-T hydrate | Chloramine-T hydrate, 95% | sodium chloro(4-methylbenzenesulfonyl)azanide hydrate | Chloramine-t hydrate,98% | AKOS015895026 | E79350 | EN300-

Storage

Room temperature,Argon charged,Desiccated

Shipped In

Normal

Panoramica

Chloramine-T hydrate is capable of oxidative cyclization to produce various heterocycles. It can also be used as a Nitrene source for aziridinations and aminohydroxylations. Additionally, it is useful as a reactant for preparation of factor Xa inhibitors as novel anticoagulants.

Specifications

Sinonimi

SCHEMBL2441113 | Sodium chloro(tosyl)amide xhydrate | Sodium chloro(tosyl)amide hydrate | Chloramine-T hydrate | Chloramine-T hydrate, 95% | sodium chloro(4-methylbenzenesulfonyl)azanide hydrate | Chloramine-t hydrate,98% | AKOS015895026 | E79350 | EN300-

Specifiche e purezza

≥95%

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged,Desiccated

Spedito in

Normal

Purezza

≥95%

Nomi e identificatori

• Pubchem Sid: 504768356
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504768356
• Sorrisi canonici: CC1=CC=C(C=C1)S(=O)(=O)[N-]Cl.O.[Na+]
• IUPAC Name: sodium;chloro-(4-methylphenyl)sulfonylazanide;hydrate
• InChIKey: BXSDMMPOQRECKB-UHFFFAOYSA-N
• INCHI: 1S/C7H7ClNO2S.Na.H2O/c1-6-2-4-7(5-3-6)12(10,11)9-8;;/h2-5H,1H3;;1H2/q-1;+1
• Isomeri SMILES: CC1=CC=C(C=C1)S(=O)(=O)[N-]Cl.O.[Na+]
• WGK Germania: 2
• CAS alternativo: 127-65-1
• PubChem CID: 16218604
• Numero UN: 3263
• Gruppo di imballaggio: III
• Peso molecolare: 227.64 (anhydrous basis)

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Benzenesulfonamides

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Benzenesulfonamides
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzenesulfonamides
• Alternative Parents: Tosyl compounds Benzenesulfonyl compounds Sulfonyls Organosulfonic acids and derivatives Organic metal halides Organic sodium salts Organic oxides Organic nitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Tosyl compound - Benzenesulfonamide - Benzenesulfonyl group - Toluene - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Organic metal halide - Organic alkali metal salt - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organosulfur compound - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as benzenesulfonamides. These are organic compounds containing a sulfonamide group that is S-linked to a benzene ring.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Meccanismi d'azione

Proprietà chimiche e fisiche

• Sensibilità: Air sensitive
• Punto di fusione (°C): 167-170° C (dec.)(lit.)
• Peso molecolare: 245.660 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 244.989 Da
• Monoisotopic Mass: 244.989 Da
• Topological Polar Surface Area: 44.500 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 231.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 3

XLogP3

Riferimenti

1. Ningyue Yu, Linzhou Zhao, Danling Cheng, Mengbin Ding, Yan Lyu, Jinhua Zhao, Jingchao Li.  (2022)  Radioactive organic semiconducting polymer nanoparticles for multimodal cancer theranostics.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:35397457] [10.1016/j.jcis.2022.03.107]

2. Xiaofeng He, Liling Xie, Xiaoshan Zhang, Fan Lin, Xiaobo Wen, Bo Teng.  (2021)  The Structural Characteristics of Collagen in Swim Bladders with 25-Year Sequence Aging: The Impact of Age.  Applied Sciences-Basel,  11  (10): (4578).  [PMID:] [10.3390/app11104578]

3. Yi Yang, Bei Tian, Xinyu Tian, Linyan Yao, Jianxi Xiao.  (2025)  Highly stable and bioactive yak type I collagen gels for accelerated healing of photoaging skin.  NEW JOURNAL OF CHEMISTRY,      [PMID:] [10.1039/D5NJ02557E]

Domande frequenti

How is this product shipped?

This product ships under standard ambient conditions. No temperature-controlled packaging is required.

What is the purity of this product?

This product is supplied at ≥95% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at room temperature, desiccated, under argon. It is supplied under an argon blanket; reseal under inert gas after each use.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 149358-73-6, the molecular formula is CH3C6H4SO2N(Cl)Na·xH2O, and the molecular weight is 227.64 (anhydrous basis) g/mol. InChIKey BXSDMMPOQRECKB-UHFFFAOYSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.