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Sodium demethylcantharidate is a synthetic chemical derivative of cantharidin, a potent blistering agent originally found in the blister beetle. It is characterized by its high toxicity and its ability to cause severe irritation and blistering when applied to the skin. SodiuM DeMethylcantharidate is also toxic if ingested, leading to symptoms such as vomiting, diarrhea, and kidney damage. Its use in veterinary medicine is primarily for the treatment of warts and tumors in horses and other livestock, but it must be handled and administered with extreme caution under the guidance of a qualified veterinarian.

13114-29-9

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13114-29-9 Usage

Uses

Used in Veterinary Medicine:
Sodium demethylcantharidate is used as a therapeutic agent for the treatment of warts and tumors in horses and other livestock. It is applied topically to induce a blistering effect that helps in the removal of the affected tissue.
Used in Research:
Due to its potent biological activity, sodium demethylcantharidate may also be used in research settings to study the mechanisms of action of cantharidin and its derivatives, as well as to develop new therapeutic agents with reduced toxicity and improved efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 13114-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,1 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13114-29:
(7*1)+(6*3)+(5*1)+(4*1)+(3*4)+(2*2)+(1*9)=59
59 % 10 = 9
So 13114-29-9 is a valid CAS Registry Number.

13114-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Endothall disodium salt

1.2 Other means of identification

Product number -
Other names sodium 7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylate

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:13114-29-9 SDS

13114-29-9Upstream product

13114-29-9Downstream Products

13114-29-9Relevant academic research and scientific papers

Crystal structures, DNA interaction and antiproliferative activities of the cobalt(II) and zinc(II) complexes of 2-amino-1,3,4-thiadiazole with demethylcantharate

Wang, Na,Lin, Qiu-Yue,Feng, Jie,Zhao, Yu-Ling,Wang, Yan-Jun,Li, Shi-Kun

experimental part, p. 3399 - 3406 (2011/01/11)

Two new mixed-ligand complexes [M(atdz)(DCA)(H2O) 2]·2H2O, (M = Co(II), Zn(II); atdz = 2-amino-1,3,4-thiadiazole, C2H3N3S; DCA = demethylcantharate, 7-oxabicyclo[2,2,1]heptane-2,3-dicarboxylate, C 8H8O5) were prepared and characterized by elemental analysis. The structures of the complexes were determined by X-ray diffraction. The crystals have empirical formulas CoC10H 19N3O9S (1) and ZnC10H 19N3O9S (2), respectively. Complex 1 and 2 are monoclinic systems with space group P21/m. The structures of the complexes assume severely distorted octahedral geometries. The DNA binding properties of the complexes were investigated by electronic absorption spectra, thermal denaturation studies, fluorescence quenching studies and viscosity measurements. All the results showed the interaction modes between the complexes and DNA were partial intercalation. The results of agarose gel electrophoresis indicated the complexes could cleave supercoiled DNA. The antiproliferative activities testing revealed that all the complexes showed weak to moderate activities against human hepatoma cells (SMMC7721) and human breast cells (MCF-7) in vitro.

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