(3-Azidopropyl)triphenylphosphonium Bromide - ≥97% , CAS No.127611-39-6

CAS: 127611-39-6 Cat. No.: A352392 Peso molecular: 426.29

GRADE & PURITY ≥97%

Synonyms

3-azidopropyl(triphenyl)phosphanium;bromide | (3-Azidopropyl)(triphenyl)phosphanium bromide | (3-Azidopropyl)triphenylphosphonium Bromide | (3-Azido-propyl)-triphenylphosphonium bromide | (3-azido-propyl)-triphenyl-phosphonium bromide | XOSIAOCZDOUXLK-UHF

Storage

Store at 2-8°C,Protected from light,Argon charged

Shipped In

Wet ice

Specifications

Sinónimos

3-azidopropyl(triphenyl)phosphanium;bromide | (3-Azidopropyl)(triphenyl)phosphanium bromide | (3-Azidopropyl)triphenylphosphonium Bromide | (3-Azido-propyl)-triphenylphosphonium bromide | (3-azido-propyl)-triphenyl-phosphonium bromide | XOSIAOCZDOUXLK-UHF

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Protected from light, Argon charged

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥97%

Nombres e identificadores

• Pubchem Sid: 504771166
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504771166
• Sonrisas canónicas: C1=CC=C(C=C1)[P+](CCCN=[N+]=[N-])(C2=CC=CC=C2)C3=CC=CC=C3.[Br-]
• IUPAC Name: 3-azidopropyl(triphenyl)phosphanium;bromide
• InChIKey: XOSIAOCZDOUXLK-UHFFFAOYSA-M
• INCHI: 1S/C21H21N3P.BrH/c22-24-23-17-10-18-25(19-11-4-1-5-12-19,20-13-6-2-7-14-20)21-15-8-3-9-16-21;/h1-9,11-16H,10,17-18H2;1H/q+1;/p-1
• Isómeros SMILES: C1=CC=C(C=C1)[P+](CCCN=[N+]=[N-])(C2=CC=CC=C2)C3=CC=CC=C3.[Br-]
• Peso molecular: 426.29
• Reaxy-Rn: 5211471
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5211471&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Phenylphosphines and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenylphosphines and derivatives
• Alternative Parents: Azo imides Azo compounds Organopnictogen compounds Organophosphorus compounds Organic bromide salts Hydrocarbon derivatives Organic cations
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Triphenylphosphine - Phenylphosphine - Azo imide - Azo compound - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organic bromide salt - Organic salt - Organophosphorus compound - Organonitrogen compound - Organic cation - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenylphosphines and derivatives. These are compounds containing a phenylphosphine, which consists of phosphine substituent bound to a phenyl group.
• 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

Propiedades químicas y físicas

• Solubilidad: Ethanol (Slightly, Heated), Methanol (Slightly), Water (Slightly)
• Sensibilidad: Light sensitive
• Punto de fusión (°C): 167-169°C
• Peso molecular: 426.300 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 7
• Exact Mass: 425.066 Da
• Monoisotopic Mass: 425.066 Da
• Topological Polar Surface Area: 14.400 Ų
• Heavy Atom Count: 26
• Formal Charge: 0
• Complexity: 383.000
• 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: 2

XLogP3

Referencias

1. Jichun Yang, Chenyu Sun, Yufang Zhang, Jianing Ji, Yuhan Wang, Qianqian Wu, Yan Zhao, Zhixin Cha, Yican Li, Xin Cui, Yao Luo, Sitong Wang, Zhizeng Wang, Sergio Benardini, Xiaohui Chen, Yang Luo.  (2025)  Endogenous stimuli-derived self-assembled DNA tetrahedron (MESH) for precise imaging and activatable mitochondrial interference therapy.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.169613]

2. Jinguo Xu, Yujun Li, Jiafeng Xu, Ruobing He, Fengchi Jiang, Jiaxue Lu, Tao Xu, Jie Wang, Chengxin Zhang.  (2026)  Renal-targeted tFNA-TPP nanoagonist treats acute kidney injury by amplifying mitophagy.  Materials Today Bio,      [PMID:41756531] [10.1016/j.mtbio.2026.102926]