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10054-29-2

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10054-29-2 Usage

General Description

Tetradecyl dihydrogen phosphate, also known as TDP or tetradecylphosphonic acid, is an organic compound with the chemical formula C14H33O4P. It is a member of the class of phosphonic acids and is commonly used as a surfactant and corrosion inhibitor in metalworking fluids, as well as in other industrial applications. TDP has excellent wetting, dispersing, and anti-foaming properties, making it useful in a wide range of formulations. It is also used as a dispersant and antiscalant in water treatment processes, where it helps to control scale formation and improve overall water quality. Tetradecyl dihydrogen phosphate is generally considered to be low in toxicity and environmentally friendly, making it a popular choice for many industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 10054-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,5 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10054-29:
(7*1)+(6*0)+(5*0)+(4*5)+(3*4)+(2*2)+(1*9)=52
52 % 10 = 2
So 10054-29-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H31O4P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-18-19(15,16)17/h2-14H2,1H3,(H2,15,16,17)

10054-29-2SDS

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 FAP-14

1.2 Other means of identification

Product number -
Other names Phosphorsaeure-monotetradecylester

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:10054-29-2 SDS

10054-29-2Downstream Products

10054-29-2Relevant articles and documents

Synthesis of Alkyl Dihydrogenphosphate by the Reaction of Alcohols and Silyl Polyphosphate

Okamoto, Yoshiki

, p. 3393 - 3394 (1985)

Alkyl dihydrogenphosphates were readily prepared by phosphorylation of alcohols with trimethylsilyl polyphosphate of polyphosphorylated silica-gel.

Alkyl and alkoxyethyl antineoplastic phospholipids

Koufaki, Maria,Polychroniou, Vanessa,Calogeropoulou, Theodora,Tsotinis, Andrew,Drees, Markus,Fiebig, Heiner H.,LeClerc, Sophie,Hendriks, Hans R.,Makriyannis, Alexandros

, p. 2609 - 2614 (1996)

Two series of phosphodiester ether lipid analogs with (N- methylmorpholino)ethyl or (N-methylpiperidino)ethyl polar head groups and long aliphatic or alkoxyethyl chains in the nonpolar portion of the molecule were synthesized as potential antineoplastic agents. The cytotoxic activity of these compounds (9-19) was evaluated in vitro against a panel of six human tumor xenografts and in two biochemical, mechanism-based screens (cdc2 kinase and cdc25 phosphatase). Analogs 13, 14, 17, and 19 showed activity in the in vitro tests. Specifically, 14 and 17 were more active than the reference compound hexadecylphosphocholine (Miltefosine, He-PC) while 13 and 19 possessed activity similar to that of the control. Of the analogs tested the one with the highest potency and least toxicity (17) has an N- methylpiperidino head group and a C16 alkyl chain. In the mechanism-based tests 11 showed weak inhibitory activity in the cdc25 phosphatase screen.

Phospholipid-induced aggregation and anthracene excimer formation

Chen, Kuan-Hung,Yang, Jye-Shane,Hwang, Chung-Yu,Fang, Jim-Min

supporting information; experimental part, p. 4401 - 4404 (2009/05/27)

(Chemical Equation) The zinc complex of anthryl bis(dipicolylamine) (1) aggregates upon binding with long-chain aliphatic phosphates and displays anthracene excimer fluorescence, which provides a new strategy toward detection of the biologically important lysophosphatidic acid in aqueous solution.

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