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4,4-Bis(diethylphosphonomethyl)biphenyl, also known as Bisphosphonate, is a phosphonate compound characterized by its high stability, low water solubility, and a colorless to pale yellow liquid appearance with a high boiling point. It is widely recognized for its applications as a flame retardant and a chelating agent, offering durable and effective solutions in various industrial settings.

17919-34-5

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17919-34-5 Usage

Uses

Used in Flame Retardant Industry:
4,4-Bis(diethylphosphonomethyl)biphenyl is used as a flame retardant for enhancing the fire resistance of plastics, textiles, and other materials. Its high stability and low water solubility contribute to its effectiveness in preventing the spread of flames and reducing the risk of fire-related incidents.
Used in Chelating Agent Applications:
In the realm of industrial processes and water treatment, 4,4-Bis(diethylphosphonomethyl)biphenyl serves as a chelating agent. It is utilized for binding and removing metal ions, thereby improving the efficiency of these processes and ensuring the quality of treated water.
However, it is crucial to acknowledge the potential toxicity and environmental concerns associated with 4,4-Bis(diethylphosphonomethyl)biphenyl. As such, its use and disposal must be meticulously managed to ensure safety and minimize any adverse impacts on human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 17919-34-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,1 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17919-34:
(7*1)+(6*7)+(5*9)+(4*1)+(3*9)+(2*3)+(1*4)=135
135 % 10 = 5
So 17919-34-5 is a valid CAS Registry Number.
InChI:InChI=1/C22H32O6P2/c1-5-25-29(23,26-6-2)17-19-9-13-21(14-10-19)22-15-11-20(12-16-22)18-30(24,27-7-3)28-8-4/h9-16H,5-8,17-18H2,1-4H3

17919-34-5 Well-known Company Product Price

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  • TCI America

  • (B1923)  4,4'-Bis(diethylphosphonomethyl)biphenyl  >95.0%(HPLC)

  • 17919-34-5

  • 1g

  • 580.00CNY

  • Detail
  • TCI America

  • (B1923)  4,4'-Bis(diethylphosphonomethyl)biphenyl  >95.0%(HPLC)

  • 17919-34-5

  • 5g

  • 1,850.00CNY

  • Detail

17919-34-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(diethoxyphosphorylmethyl)-4-[4-(diethoxyphosphorylmethyl)phenyl]benzene

1.2 Other means of identification

Product number -
Other names 4,4-Bis(diethylphosphonomethyl)biphenyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17919-34-5 SDS

17919-34-5Relevant academic research and scientific papers

Synthesis of conjugated polymers containing biphenyl group and their electro-optical properties

Park, Lee Soon,Han, Yoon Soo,Kim, Sang Dae

, p. 431 - 434 (2000)

Two types of conjugated polymer, poly(MEHPV-co-BPV)s and poly(MEHPV-alt-BPV), were synthesized by dehydrohalogenation and Honer-Emmons condensation, respectively. Single layer type light-emitting diodes were fabricated utilizing synthesized polymers and t

Hybrid cyclic dimers of divacant heteropolyanions: Synthesis, mass spectrometry (MALDI-TOF and ESI-MS) and NMR multinuclear characterisation

Mayer, Cedric R.,Herve, Maryline,Lavanant, Helene,Blais, Jean-Claude,Secheresse, Francis

, p. 973 - 977 (2004)

In the field of organic-inorganic hybrid composites, functionalized polyoxometalates constitute a special class of inorganic nanobuilding blocks (NBBs). This study represents a first approach related to the formation of new oligomeric hybrid species based on the reaction of bis(electrophilic) groups with a divacant heteropolyanion as the NBB. Bis(phosphonates) such as para-H2O3PCH2(C6H4) nCH2PO3H2 (n = 1 or 2) have been treated with the divacant heteropolyanion [γ-SiW10O 36]8- to form the hybrid cyclic dimer [H 2((SiW10O36) (O=PCH2(C 6H4)nCH2P=O)]2] 6-. MALDI-TOF and ESI mass spectrometry have been used as essential analytical techniques for the characterization of such composite systems. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

OPTICAL DATA COMMUNICATION SYSTEM COMPRISING PARA-PHENYLENEVINYLENES AND SPECIFIC PARA-PHENYLENEVINYLENES

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Page/Page column 49; 51, (2020/01/08)

An optical data communication system comprising para-phenylenevinylenes, a receiver for an optical data communication system comprising para-phenylenevinylenes, a transmitter for an optical data communication system comprising para-phenylenevinylenes, the use of para- phenylenevinylenes in an optical data communication system, specific para-phenylenevinylenes and their preparation.

Substituent effect on the photochemical and photophysical properties of 4,4′-distyrylbiphenyl derivatives

Sakurai, Hiroya,Arai, Tatsuo

, p. 1337 - 1339 (2017/12/26)

Photochemical properties of 4,4′-distyrylbiphenyl (DSBP) derivatives have been studied. While the introduction of methoxy groups at meta-positions does not influence the photoisomerization of DSBP, the introduction of methyl substituents at the biphenyl moiety (MDSBP) changed the photoisomerization from one-way cis-to-trans photoisomerization for DSBP to cistrans mutual photoisomerization for MDSBP.

Dendritic effect on the photoisomerization of 4,4′-distyrylbiphenyl in aqueous solution

Sakurai, Hiroya,Arai, Tatsuo

, p. 911 - 913 (2016/10/26)

Newly synthesized 4,4′-distyrylbiphenyl-cored water-soluble dendrimers underwent trans-to-cis photoisomerization, while the core 4,4′-distyrylbiphenyl underwent cis-to-trans one-way photoisomerization.

NOVEL LIQUID CRYSTALLINE COMPOUND, LIQUID CRYSTAL COMPOSITION, OPTICAL ELEMENT AND OPTICAL DISPLAY DEVICE

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Paragraph 0087, (2018/10/16)

PROBLEM TO BE SOLVED: To provide a novel liquid crystalline compound that is low in dielectric anisotropy, has responsiveness, and changes its birefringence by application of voltage. SOLUTION: The present invention provides a compound represented by formula (1) (In the formula (1), R1, R2 and R3 independently represent a hydrogen atom or C1-C10 alkyl, in the alkyl, at least one -CH2- may be substituted by -O-, -S-, -CO-, or -SiH2-, and at least one -(CH2)2- may be substituted by -CH=CH-or -C≡C-. n is an integer of 0-4. m is an integer of 1 or 2. Z1 and Z2 are -CH=CH-). SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

Novel hole transporting materials with a linear π-conjugated structure for highly efficient perovskite solar cells

Wang, Junjie,Wang, Shirong,Li, Xianggao,Zhu, Lifeng,Meng, Qingbo,Xiao, Yin,Li, Dongmei

supporting information, p. 5829 - 5832 (2014/05/20)

Novel small-molecule hole transporting materials (HTMs) with a linear π-conjugated structure have been synthesized. The perovskite solar cell based on 2TPA-2-DP as the HTM exhibits an encouraging power conversion efficiency of 9.1% under AM 1.5 G (100 mW cm-2) illumination, which is the first demonstration of an effective perovskite solar cell using a linear structured HTM. This journal is the Partner Organisations 2014.

Synthesis, characterization and properties of a novel triphenylamine substituted Oligo(phenylene vinylene)

Xu,Chen,Huang,Shi,Wang

experimental part, p. 3929 - 3935 (2010/11/16)

A novel hole transport material of triphenylamine-substituted oligo(phenylene vinylene) of 4,4'-bis-[2-[4-[N,N-bis-(4-bromophenylamino)]- phenyl-1-yl]-vinyl-1-yl]-1,1'-biphenyl was synthesized. Its molecular structure was characterized by FTIR and 1

Synthesis, fluorescence, and two-photon absorption of a series of elongated rodlike and banana-shaped quadrupolar fluorophores: A comprehensive study of structure-property relationships

Mongin, Olivier,Porres, Laurent,Charlot, Marina,Katan, Claudine,Blanchard-Desce, Mireille

, p. 1481 - 1498 (2008/02/04)

An extensive series of push-push and pull-pull derivatives was prepared from the symmetrical functionalization of an ambivalent core with conjugated rods made from arylene-vinylene or arylene-ethynylene building blocks, bearing different acceptor or donor

STILBENE DERIVATIVE, METHOD FOR PRODUCING THE SAME, AND ELECTROPHOTOGRAPHIC PHOTORECEPTOR

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Page/Page column 41, (2010/02/13)

PROBLEM TO BE SOLVED: To provide a stilbene derivative having predetermined substituents in the intramolecular triphenylamine structure, thus improved in compatibility with binder resin and yielding predetermined drum sensitivity properties, to provide a method for producing the stilbene derivative, and to provide an electrophotographic photoreceptor containing the stilbene derivative. SOLUTION: The stilbene derivative is represented by general formula(1) ( wherein, A is a bivalent organic group containing a substituted or nonsubstituted aromatic ring; and R1 to R18 are each H, a substituted or nonsubstituted 1-6C alkyl or the like, wherein at least two of R1 to R18 may be bound to or condensed with each other to form a carbocyclic group or heterocyclic group ). The method for producing the stilbene derivative comprises carrying out a reaction between a specific formylated triphenylamine derivative and a specific diphosphoric ester derivative in the presence of a base. The electrophotographic photoreceptor containing the stilbene derivative is also provided.

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