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Phenol, 4-(1,1,3,3-tetramethylbutyl)-, dihydrogen phosphate, also known as 4-(tetramethylbutyl)phenol dihydrogen phosphate or TMPP, is a chemical compound with the molecular formula C14H25O4P. It is a derivative of phenol, featuring a tetramethylbutyl group attached to the para position of the phenol ring. TMPP is a white crystalline solid that is soluble in water and organic solvents. Phenol, 4-(1,1,3,3-tetramethylbutyl)-, dihydrogen phosphate is primarily used as a scale inhibitor and corrosion inhibitor in various industrial applications, such as water treatment, oil and gas production, and cooling systems. Its ability to prevent the formation of calcium carbonate and other scale-forming minerals makes it an effective additive in these applications. Additionally, TMPP exhibits low toxicity and is considered environmentally friendly, making it a preferred choice in many industries.

1986-91-0

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1986-91-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1986-91-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,8 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1986-91:
(6*1)+(5*9)+(4*8)+(3*6)+(2*9)+(1*1)=120
120 % 10 = 0
So 1986-91-0 is a valid CAS Registry Number.

1986-91-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name mono[4-(1,1,3,3-tetramethylbutyl)phenyl]phosphate

1.2 Other means of identification

Product number -
Other names [p-(1,1,3,3-tetramethylbutyl) phenyl] phosphoric 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:1986-91-0 SDS

1986-91-0Upstream product

1986-91-0Downstream Products

1986-91-0Relevant academic research and scientific papers

Fragment-based substrate activity screening method for the identification of potent inhibitors of the Mycobacterium tuberculosis phosphatase PtpB

Soellner, Matthew B.,Rawls, Katherine A.,Grundner, Christoph,Alber, Tom,Ellman, Jonathan A.

, p. 9613 - 9615 (2008/02/13)

A new substrate-based fragment approach for the identification of novel PTP inhibitors is presented. This method was applied to Mycobacterium tuberculosis PtpB, a promising new target for the treatment of tuberculosis. This resulted in the development of the most potent PtpB inhibitor reported to date (0.22 μM) with low molecular weight and good selectivity against a panel of other protein tyrosine phosphatases. Copyright

Synthesis of mono-and dialkylphosphates by the reactions of hydroxycompounds with the phosphorus pentaoxide under microwave irradiation

Elias, Abdelhamid,Didi, M. Amine,Villemin, Didier,Semaoune,Ouattas

, p. 2599 - 2607 (2007/10/03)

The reactions of phosphorus pentoxide with two alcohols and one phenol were performed in different conditions under microwave irradiation. The products (alkylphosphates and dialkylphosphates) were identical to those formed by classic heating and were obtained with better yields. The speed of the reaction was increased by a factor from 100 to 4000.

NMR study of the action of phophorus pentoxide on p-(1,1,3,3-tetramethylbutyl) phenol

Didi, Mohamed-Amine,Azzouz, Abdelkrim,Rodehuser, Ludwig,Dumitriu, Emil

, p. 631 - 639 (2007/10/03)

The reaction between P2O5 and p-(1,1,3,3'-tetramethylbutyl)phenol was investigated through 31P-NMR. The considered kinetic model showed that only time and, to a lesser extent, the temperature of the reaction, seem to influence the yield. The reactant mole ratio exhibits no effect upon the MOPPA:DOPPA ratio. Attempts based on a 2 3 factorial experiment design allowed to confirm these results. The tripyroesters were identified as being the longest intermediates detected by NMR. In the reaction mixture no traces of phosphoric triester (TOPPA) were detected.

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