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Dibutylphosphinic acid, also known as DBPA, is an organophosphorus compound with the chemical formula C8H17PO2. It is a colorless liquid with a mild, characteristic odor and is soluble in water. DBPA is primarily used as a corrosion inhibitor in various industrial applications, such as oil and gas pipelines, cooling systems, and water treatment processes. It is effective in preventing the formation of rust and other types of corrosion by forming a protective film on metal surfaces. Additionally, DBPA is employed as a flame retardant and a plasticizer in the production of certain plastics. Due to its potential health and environmental risks, proper handling and disposal procedures are essential when working with dibutylphosphinic acid.

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  • 866-32-0 Structure
  • Basic information

    1. Product Name: Dibutylphosphinic acid
    2. Synonyms: Dibutylphosphinic acid
    3. CAS NO:866-32-0
    4. Molecular Formula: C8H19O2P
    5. Molecular Weight: 178.209
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 866-32-0.mol
  • Chemical Properties

    1. Melting Point: 70.5-71 °C
    2. Boiling Point: 341.7°Cat760mmHg
    3. Flash Point: 160.4°C
    4. Appearance: /
    5. Density: 0.977g/cm3
    6. Vapor Pressure: 1.44E-05mmHg at 25°C
    7. Refractive Index: 1.434
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 3.42±0.50(Predicted)
    11. CAS DataBase Reference: Dibutylphosphinic acid(CAS DataBase Reference)
    12. NIST Chemistry Reference: Dibutylphosphinic acid(866-32-0)
    13. EPA Substance Registry System: Dibutylphosphinic acid(866-32-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 866-32-0(Hazardous Substances Data)

866-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 866-32-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,6 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 866-32:
(5*8)+(4*6)+(3*6)+(2*3)+(1*2)=90
90 % 10 = 0
So 866-32-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H19O2P/c1-3-5-7-11(9,10)8-6-4-2/h3-8H2,1-2H3,(H,9,10)

866-32-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name dibutylphosphinic acid

1.2 Other means of identification

Product number -
Other names Dibutyl-phosphinsaeure

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:866-32-0 SDS

866-32-0Relevant articles and documents

Synthesis and molecular structure of tetranuclear Cu4P4 complexes with R2P-O-PR2 ligands

Zhao, Yalei,Zhou, Yongbo,Chen, Tieqiao,Yin, Shuang-Feng,Han, Li-Biao

, p. 36 - 39 (2014)

The reaction of secondary phosphine oxides R2P(O)H 1 with Cu(OAc)2 under nitrogen atmosphere produced complexes [(R2P)2O(CuOAc)2]2 2. A rapid ligand exchange took place when treating complexes 2 with NH4Cl to generate [(R2P)2O(CuCl)2]2 3 in good yields. The structures of 3 were determined by X-ray crystallography, showing that the geometries of these tetranuclear copper complexes vary with the R group of the phosphorus units. Compared to complexes 2 which are air sensitive, complexes 3 are stable under air.

INVESTIGATION OF THE REACTION BETWEEN DIALKYLPHOSPHINE OXIDES AND CARBONTETRACHLORIDE

Aksnes, Gunnar,Majewski, Piotr

, p. 261 - 274 (2007/10/02)

The time dependent formation of intermediates and end products in the reaction between Et2P(O)H and CCl4 is analysed using (31)P-NMR technique.The various reaction steps are studied separately in order to elucidate the overall mechanism.A key step is the disproportionation of Et2P(O)H catalysed by Et2PCl and Et2P(O)Cl, in a cyclic process, the latter being produced initially by the reaction between Et2P(O)H and CCl4.The diethylphosphine formed during disproportionation reacts immediately with CCl4, driving the reaction through the intermediates, Et2PCl and Et2PCCl3which react with Et2P(O)OH producing Et2P(O)Cl, (Et2PO)2O, and Et2P(O)CHCl2, as end products.The influence of the substituents on rate and product yields was studied with n-propyl, n-butyl, n-octyl, and allyl as substituents in the dialkylphosphine oxide.

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