Diphenyl-1-pyrenylphosphine - ≥95% , CAS No.110231-30-6

CAS: 110231-30-6 Cat. No.: D154318 Molecular Weight: 386.43 EC Number: 679-807-0

GRADE & PURITY ≥95%

Synonyms

DPPP | DTXSID60149186 | MFCD00278755 | ZB1733 | DSYGKYCYNVHCNQ-UHFFFAOYSA-N | DIPHENYL-PYREN-1-YL-PHOSPHANE | HY-118159 | DPP-P | AS-59133 | diphenyl(pyren-1-yl)phosphane | Diphenyl-1-pyrenylphosphine | Diphenyl(pyren-1-yl)phosphine | diphenylpyrenylphosp

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Synonyms

DPPP | DTXSID60149186 | MFCD00278755 | ZB1733 | DSYGKYCYNVHCNQ-UHFFFAOYSA-N | DIPHENYL-PYREN-1-YL-PHOSPHANE | HY-118159 | DPP-P | AS-59133 | diphenyl(pyren-1-yl)phosphane | Diphenyl-1-pyrenylphosphine | Diphenyl(pyren-1-yl)phosphine | diphenylpyrenylphosp

Specifications & Purity

≥95%

Storage

Store at 2-8°C, Argon charged

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥95%

Names and Identifiers

• Pubchem Sid: 504757005
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504757005
• Canonical Smiles: C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=C4C=CC5=CC=CC6=C5C4=C(C=C6)C=C3
• IUPAC Name: diphenyl(pyren-1-yl)phosphane
• InChIKey: DSYGKYCYNVHCNQ-UHFFFAOYSA-N
• INCHI: 1S/C28H19P/c1-3-10-23(11-4-1)29(24-12-5-2-6-13-24)26-19-17-22-15-14-20-8-7-9-21-16-18-25(26)28(22)27(20)21/h1-19H
• Isomeric SMILES: C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=C4C=CC5=CC=CC6=C5C4=C(C=C6)C=C3
• Molecular Weight: 386.43
• Reaxy-Rn: 9798358
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9798358&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Phenylphosphines and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenylphosphines and derivatives
• Alternative Parents: Pyrenes Phenanthrenes and derivatives Naphthalenes Organic phosphines and derivatives Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Triphenylphosphine - Pyrene - Phenanthrene - Naphthalene - Phenylphosphine - Phosphine - Organopnictogen compound - Hydrocarbon derivative - Organophosphorus compound - Aromatic homopolycyclic compound
• Description: 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

Chemical and Physical Properties

• Sensitivity: heat sensitive；Air sensitive
• Melt Point(°C): 174-178℃
• Molecular Weight: 386.400 g/mol
• XLogP3: 7.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 3
• Exact Mass: 386.122 Da
• Monoisotopic Mass: 386.122 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 29
• Formal Charge: 0
• Complexity: 527.000
• 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: 1

References

1. Yu Zhang, Dekun Cheng, Zhangtie Wang, Yiwen Guo, Ming Chang, Ruijie Liu.  (2022)  Protective Effect of Orbitides from Linseed (Linum usitatissimum L.) against Ultraviolet B-induced Photoaging in Zebrafish.  PHOTOCHEMISTRY AND PHOTOBIOLOGY,      [PMID:36484266] [10.1111/php.13758]

2. Chae-Yeon Woo, Gi-Hyeok Lee, Kyung-Jik Lim, Jun-Won Kang.  (2025)  Utilizing onion peel extract as photosensitizer combined with 405 nm blue light to control Salmonella Typhimurium on eggshells.  JOURNAL OF FOOD SCIENCE,  90  (3): (e70167).  [PMID:40145615] [10.1111/1750-3841.70167]

3. Ruoxin Chen, Jiahao Ren, Zhenlong Zhou, Wenjun Zhang, Jianyu Su.  (2025)  Integrating zebrafish model and network pharmacology for screening and identification of edible herbs with therapeutic potential of anti-photoaging: A promising drug Gentiana rigescens Franch..  Food Bioscience,      [PMID:] [10.1016/j.fbio.2025.107278]