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156125-36-9

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156125-36-9 Usage

General Description

Phosphonic acid, (11-mercaptoundecyl)- is a chemical compound with the molecular formula C11H25O3PS. It is a phosphonic acid with an 11-mercaptoundecyl group attached. Phosphonic acid, (11-mercaptoundecyl)- is used in various applications, including as a coupling agent for surface modifications and as an adhesion promoter in adhesive formulations. It is also utilized as a corrosion inhibitor in various industries, such as the automotive and metalworking sectors. Additionally, it has potential use in biomedical applications due to its ability to modify the surfaces of biomaterials and enhance their biocompatibility. Overall, phosphonic acid, (11-mercaptoundecyl)- has diverse uses in industries and research, making it a valuable and versatile chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 156125-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,1,2 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 156125-36:
(8*1)+(7*5)+(6*6)+(5*1)+(4*2)+(3*5)+(2*3)+(1*6)=119
119 % 10 = 9
So 156125-36-9 is a valid CAS Registry Number.

156125-36-9 Well-known Company Product Price

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  • Aldrich

  • (754269)  11-Mercaptoundecylphosphonic acid  97%

  • 156125-36-9

  • 754269-500MG

  • 2,895.75CNY

  • Detail

156125-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-sulfanylundecylphosphonic acid

1.2 Other means of identification

Product number -
Other names 11-Mercaptoundecylphosphonic acid

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:156125-36-9 SDS

156125-36-9Downstream Products

156125-36-9Relevant articles and documents

Detection of discrete interactions upon rupture of au microcontacts to self-assembled monolayers terminated with -S(CO)CH3 or -SH

Skulason, Hjalti,Frisbie, C. Daniel

, p. 9750 - 9760 (2000)

Pulloff forces were measured under solvent for Au-coated atomic force microscopy (AFM) tips in contact with -S-acetate-, -O-acetate-, -SH-, or -OH-terminated self-assembled monolayers (SAMs). The SAMs were formed by adsorption of ω-functionalized undecylphosphonic acids on metal oxide substrates. In ethanol and hexadecane, the mean force required to rupture Au/S-acetate microcontacts was 7 times greater than the mean force required to break Au/O-acetate contacts, consistent with the known affinity of S-containing functional groups for Au. Further, rupture force histograms for Au/S-acetate microcontacts under ethanol or hexadecane showed 0.1 nN periodicity. Rupture forces for Au/-SH microcontacts were 4 times greater than for Au/-OH microcontacts under ethanol, and the rupture force histograms showed the same 0.1 nN periodicity. We have assigned this 0.1 nN force quantum to rupture of individual chemical bonds and have estimated the bond energy to be on the order of 10 kJ/mol. The specific interaction corresponding to this energy appears to be abstraction of Au atoms from the tip surface upon pulloff. Our ability to detect these discrete interactions was a function of the solvent in which the measurements were made. For example, in water there was no difference in the mean pulloff force for Au/S-acetate and Au/O-acetate contacts and the histograms did not exhibit periodicity. In general, mean rupture forces for tip-SAM microcontacts are strongly solvent-dependent. To observe single bond rupture forces directly, we argue that the tip-substrate interfacial energy must be negative and larger in absolute value than the substrate-solvent and tip-solvent interfacial energies [i.e., |γsubstrate-tip| > (γtip-solvent + γsubstrate-solvent)]. Otherwise, nonspecific solvent exclusion effects dominate the microcontact adhesion. These measurements show that, whereas rupture forces for tip-SAM microcontacts are solvent-dependent, these forces can be sensitive, under the right conditions, to fluctuations in the number of discrete chemical interactions.

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