DIPPMPO - ≥95% , CAS No.527704-58-1

CAS: 527704-58-1 Cat. No.: D377986 Peso molecular: 263.27 Número EC: 817-444-3

GRADE & PURITY ≥95%

Synonyms

SCHEMBL829886 | EN300-1587728 | DIPPMPO | 5-(Diisopropoxyphosphoryl)-5-methyl-1-pyrroline N-oxide | 2-[BIS(PROPAN-2-YLOXY)PHOSPHORYL]-2-METHYL-3,4-DIHYDRO-2H-PYRROL-1-IUM-1-OLATE | 5-(diisopropoxyphosphoryl)-5-methyl-1-pyrroline-n-oxide | 5-(Diisopropoxyp

Storage

Protected from light,Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Descripción general

DIPPMPO is, beside DEPMPO , the most efficient spin trap for the|in vitro|detection of O-, N-, S-, and C-centered free radicals. DIPPMPO is more lipophilic (K|p|=2.1) than DEPMPO with a longer life-time than DMPO .

Application：

DIPPMPO is an efficient spin trap to detect free radicals

Specifications

Sinónimos

SCHEMBL829886 | EN300-1587728 | DIPPMPO | 5-(Diisopropoxyphosphoryl)-5-methyl-1-pyrroline N-oxide | 2-[BIS(PROPAN-2-YLOXY)PHOSPHORYL]-2-METHYL-3, 4-DIHYDRO-2H-PYRROL-1-IUM-1-OLATE | 5-(diisopropoxyphosphoryl)-5-methyl-1-pyrroline-n-oxide | 5-(Diisopropoxyp

Especificaciones y pureza

≥95%

Condiciones de almacenamiento de almacenamiento

Protected from light, Store at -20°C, Argon charged

Enviado en

Ice chest + Ice pads

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

Pureza

≥95%

Nombres e identificadores

• Pubchem Sid: 504763281
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504763281
• Sonrisas canónicas: CC(C)OP(=O)(C1(CCC=[N+]1[O-])C)OC(C)C
• IUPAC Name: 2-di(propan-2-yloxy)phosphoryl-2-methyl-1-oxido-3,4-dihydropyrrol-1-ium
• InChIKey: JQERKXDWSAKBRU-UHFFFAOYSA-N
• INCHI: 1S/C11H22NO4P/c1-9(2)15-17(14,16-10(3)4)11(5)7-6-8-12(11)13/h8-10H,6-7H2,1-5H3
• Isómeros SMILES: CC(C)OP(=O)(C1(CCC=[N+]1[O-])C)OC(C)C
• Peso molecular: 263.27
• Reaxy-Rn: 9326036
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9326036&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Organic phosphonic acids and derivatives
      • Subclass Phosphonic acid diesters

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Organic phosphonic acids and derivatives
• Subclass: Phosphonic acid diesters
• Intermediate Tree Nodes: Not available
• Direct Parent: Dialkyl alkylphosphonates
• Alternative Parents: Phosphonic acid esters Pyrrolines Nitrones Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organophosphorus compounds Organooxygen compounds Organonitrogen compounds Organic salts Organic oxides Hydrocarbon derivatives Organic cations
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Dialkyl alkylphosphonate - Phosphonic acid ester - Pyrroline - Nitrone - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Azacycle - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organic salt - Organooxygen compound - Organophosphorus compound - Hydrocarbon derivative - Organic cation - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as dialkyl alkylphosphonates. These are compounds containing a phosphonic acid that is diesterified with alkyl groups, and the phosphorus atom is also directly attached to an alkyl 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: Soluble in water, 100% ethanol or methylene chloride.
• Sensibilidad: Air sensitive；Moisture sensitive；Light sensitive
• Peso molecular: 263.270 g/mol
• XLogP3: 0.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 263.129 Da
• Monoisotopic Mass: 263.129 Da
• Topological Polar Surface Area: 64.300 Ų
• Heavy Atom Count: 17
• Formal Charge: 0
• Complexity: 339.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Zhimin Gong, Gaobo Wang, Shuai Shao, Mengjie Wang, Kun Lu, Shixiang Gao.  (2021)  Co-degradation of coexisting pollutants methylparaben (mediators) and amlodipine in enzyme-mediator systems: Insight into the mediating mechanism.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:34523479] [10.1016/j.jhazmat.2021.127112]

2. Yunzhe Zheng, Xinhao Wang, Yudan Dong, Xiaoyu Wu, Donghua Xie, Yang Liu, Peng Zhou, Zhaokun Xiong, Chuan-Shu He, Bo Lai.  (2024)  Overlooked role of boron precursors in tuning engineered zero-valent iron to activate peracetic acid for sustainable micropollutant oxidation.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2024.124580]

3. Sichu Xing, Chundi Zhou, Minghao Sui.  (2025)  Activated carbon-supported nano zero-valent iron (nZVI@AC) for enhanced peracetic acid activation in Fenton-like degradation of sulfamethoxazole.  MATERIALS RESEARCH BULLETIN,      [PMID:] [10.1016/j.materresbull.2025.113780]

4. Nabi Bux, Danruo Luo, Shan Qian, He Guo, Sadam Hussain Tumrani, Razium Ali Soomro, Guodong Zhang, Qiuling Ma, Jian Zhou, Tiecheng Wang.  (2026)  Dual heteroatom engineering-modulated cobalt catalysts for peracetic acid activation realized superior sulfadiazine degradation in water.  JOURNAL OF ENVIRONMENTAL MANAGEMENT,      [PMID:41763053] [10.1016/j.jenvman.2026.129149]