Cloramina T trihidrato - AR, ≥98%(T) , CAS No.7080-50-4

CAS: 7080-50-4 Cat. No.: C104061 Peso molecular: 281.69 Beilstein Registry Number: 3924168 Número EC: 615-172-8 PubChem CID: 517414

GRADE & PURITY AR, ≥98%(T)

Synonyms

Cloraseptina | Euclorina | Bencenosulfonamida, N-cloro-4-metil-, sal sódica, trihidrato | Disifin | HALAMID AQUA | Sal sódica de p-toluenosulfonamida | HY-U00087 | Derivado sódico de N-cloro-p-toluenosulfonamida trihidrato | CLORAMINA-T TRIHYDRA

Storage

Protected from light,Argon charged,Room temperature

Shipped In

Normal

Descripción general

para la detección de halógenos y bromato

Specifications

Sinónimos

Cloraseptina | Euclorina | Bencenosulfonamida, N-cloro-4-metil-, sal sódica, trihidrato | Disifin | HALAMID AQUA | Sal sódica de p-toluenosulfonamida | HY-U00087 | Derivado sódico de N-cloro-p-toluenosulfonamida trihidrato | CLORAMINA-T TRIHYDRA

Especificaciones y pureza

AR, ≥98%(T)

Condiciones de almacenamiento de almacenamiento

Protected from light, Argon charged, Room temperature

Enviado en

Normal

Grado

AR

Pureza

≥98%(T)

Nombres e identificadores

• Pubchem Sid: 504759000
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504759000
• Sonrisas canónicas: CC1=CC=C(C=C1)S(=O)(=O)[N-]Cl.O.O.O.[Na+]
• IUPAC Name: sodium;chloro-(4-methylphenyl)sulfonylazanide;trihydrate
• InChIKey: NZYOAGBNMCVQIV-UHFFFAOYSA-N
• INCHI: 1S/C7H7ClNO2S.Na.3H2O/c1-6-2-4-7(5-3-6)12(10,11)9-8;;;;/h2-5H,1H3;;3*1H2/q-1;+1
• Isómeros SMILES: CC1=CC=C(C=C1)S(=O)(=O)[N-]Cl.O.O.O.[Na+]
• WGK Alemania: 2
• PubChem CID: 517414
• Número ONU: 3263
• Peso molecular: 281.69
• Beilstein: 3924168

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: 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: Benzenesulfonamide - Tosyl compound - Benzenesulfonyl group - Toluene - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Organic metal halide - Organic alkali metal salt - Organic sodium salt - Organic salt - Organic oxygen compound - Organosulfur compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound
• Descripción: 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

Objetivos asociados (humanos)

EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

Discover Target: EHMT2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Objetivos asociados (no humanos)

GCN5 Histone acetyltransferase GCN5 (89 Activities)

Discover Target: GCN5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)

Discover Target: ffp

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in water and ethyl alcohol. Insoluble in benzene and ethers.
• Sensibilidad: light & Moisture & air sensitive
• Punto de inflamación (°F): 377.6 °F
• Punto de inflamación (°C): 192 °C
• Punto de fusión (°C): 167-170°C
• Peso molecular: 281.690 g/mol
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1
• Exact Mass: 281.01 Da
• Monoisotopic Mass: 281.01 Da
• Topological Polar Surface Area: 46.500 Ų
• Heavy Atom Count: 16
• 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: 5

XLogP3

Referencias

1. Yuedan Xu, Yi Sun, Wei Liu, Zhiwei Shi, Xinyang Jin, Jiawei Xu, Xinni Pan, Zhixin Zhang, Baiping Fu, Ling Zhang.  (2022)  Effects of an orthodontic primer containing amorphous fluorinated calcium phosphate nanoparticles on enamel white spot lesions.  Journal of the Mechanical Behavior of Biomedical Materials,      [PMID:36379092] [10.1016/j.jmbbm.2022.105567]

2. Fangmiao Yu, Chuhong Zong, Shujie Jin, Jiawen Zheng, Nan Chen, Ju Huang, Yan Chen, Fangfang Huang, Zuisu Yang, Yunping Tang, Guofang Ding.  (2018)  Optimization of Extraction Conditions and Characterization of Pepsin-Solubilised Collagen from Skin of Giant Croaker (Nibea japonica).  Marine Drugs,  16  (1): (29).  [PMID:29342895] [10.3390/md16010029]

3. An Jie, Zhou Qin, Chu Kaile, Chen Siyuan, Niu Chenliang, Zhang Weiming, Gao Jie, Li Min, Cao Jianbo, Lv Junping, Zhang Di, Wu Zhifang, Li Sijin, Wei Hua.  (2025)  Tumor microenvironment-responsive precise delivery nanocarrier potentiating synchronous radionuclide therapy and chemotherapy against cancer.  JOURNAL OF NANOBIOTECHNOLOGY,  23  (1): (1-16).  [PMID:40229814] [10.1186/s12951-025-03364-4]