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CAS

  • or
Etamsylate, also known as diethylaminoethoxyhexestrol, is a synthetic estrogen derivative with a white solid appearance. It possesses both hemostatic and anti-coagulant properties, making it a versatile pharmaceutical agent for various medical applications.

2624-44-4

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2624-44-4 Usage

Uses

Used in Hemorrhage Control:
Etamsylate is used as a hemostatic agent for controlling excessive bleeding, particularly in cases of trauma or surgical procedures. Its ability to promote blood clotting helps prevent blood loss and stabilize patients.
Used in Anti-Coagulation Therapy:
In addition to its hemostatic properties, Etamsylate also functions as an anti-coagulant, making it useful in preventing blood clot formation and reducing the risk of thrombotic events, such as deep vein thrombosis and pulmonary embolism.
Used in Prostaglandin Synthesis Inhibition:
Etamsylate is used as a prostaglandin synthesis inhibitor, which helps regulate the production of prostaglandins that play a role in inflammation, pain, and blood clotting. By inhibiting prostaglandin synthesis, Etamsylate can help manage inflammation and pain associated with various conditions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Etamsylate is used as an active ingredient in various formulations, such as tablets and injections, for the treatment of hemorrhage, blood clotting disorders, and inflammatory conditions. Its dual action as a hemostatic and anti-coagulant makes it a valuable compound in the development of medications for diverse medical needs.

Clinical Use

Short-term treatment of blood loss in menorrhagiaProphylaxis of surgical bleeding (unlicensed)

Drug interactions

Potentially hazardous interactions with other drugs None known

Metabolism

Etamsylate is excreted unchanged, mainly in the urine.

Check Digit Verification of cas no

The CAS Registry Mumber 2624-44-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,2 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2624-44:
(6*2)+(5*6)+(4*2)+(3*4)+(2*4)+(1*4)=74
74 % 10 = 4
So 2624-44-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H6O5S.C4H11N/c7-4-1-2-5(8)6(3-4)12(9,10)11;1-3-5-4-2/h1-3,7-8H,(H,9,10,11);5H,3-4H2,1-2H3

2624-44-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (E1145)  Etamsylate  >98.0%(HPLC)(T)

  • 2624-44-4

  • 1g

  • 590.00CNY

  • Detail
  • TCI America

  • (E1145)  Etamsylate  >98.0%(HPLC)(T)

  • 2624-44-4

  • 5g

  • 1,750.00CNY

  • Detail
  • Sigma-Aldrich

  • (E1830000)  Etamsylate  European Pharmacopoeia (EP) Reference Standard

  • 2624-44-4

  • E1830000

  • 1,880.19CNY

  • Detail

2624-44-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-Dihydroxybenzenesulfonic acid N-ethylethanamine (1:1)

1.2 Other means of identification

Product number -
Other names Benzenesulfonic acid,2,5-dihydroxy-,compd. with N-ethylethanamine

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:2624-44-4 SDS

2624-44-4Synthetic route

dobesilate
88-46-0

dobesilate

diethylamine
109-89-7

diethylamine

ethamsylate
2624-44-4

ethamsylate

Conditions
ConditionsYield
In cyclohexane at 65 - 70℃; Solvent; Temperature;85%
In ethanol at 25℃; for 1.5h; Temperature;
benzene-1,4-diyl diacetate
1205-91-0

benzene-1,4-diyl diacetate

ethamsylate
2624-44-4

ethamsylate

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: chlorosulfonic acid / 1,2-dichloro-ethane / 2.5 h / 5 - 90 °C
2: sodium hydroxide; water / 2 h / 40 °C
3: ethanol / 1.5 h / 25 °C
View Scheme
ethamsylate
2624-44-4

ethamsylate

p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

ammonium salt of 2,5-dihydroxybenzenesulphonic acid monotosylate

ammonium salt of 2,5-dihydroxybenzenesulphonic acid monotosylate

Conditions
ConditionsYield
With ammonium hydroxide In N-methyl-acetamide; water
With ammonium hydroxide In N-methyl-acetamide; water
ethamsylate
2624-44-4

ethamsylate

C4H11N*C6H4O5S

C4H11N*C6H4O5S

Conditions
ConditionsYield
With nitric acid; potassium thioacyanate; copper; potassium nitrate; 4-(pyridyl-2-azo)resorcinol In ethanol; water at 30℃; for 0.333333h; pH=5; aq. buffer;100 %Spectr.
With dihydrogen peroxide; horseradish peroxidase; phenol In aq. phosphate buffer; dimethyl sulfoxide at 20℃; pH=7; Kinetics; Enzymatic reaction;

2624-44-4Downstream Products

2624-44-4Relevant articles and documents

C10H17NO5S.1/20H2O compound

-

Paragraph 0035; 0038; 0040; 0043; 0045; 0048, (2020/01/25)

The invention discloses a C10H17NO5S.1/20H2O compound and a preparation method thereof. The compound is measured by using a powder X-ray diffraction measurement method, and shows characteristic diffraction peaks represented by a diffraction angle of 2theta +/- 0.2 degrees at the places of 13.4 degrees, 17.2 degrees, 20.5 degrees, 21.4 degrees, 23.7 degrees, 24.5 degrees, 26.9 degrees, 28.0 degreesand 34.0 degrees. The C10H17NO5S.1/20H2O compound prepared by the preparation method has the advantages of good thermal stability, high purity, and weak hygroscopicity, has a simple process, a high yield and strong repeatability, and is suitable for industrial production.

Method for producing high-purity etamsylate

-

Paragraph 0025; 0029-0036, (2019/03/29)

The invention discloses a method for producing high-purity etamsylate. The method comprises the following steps: carrying out a sulfonation reaction on hydroquinone serving as an initial material, a sulfonating agent, a dispersing agent and an organic solvent to obtain 2,5-dihydroxybenzenesulfonic acid; cooling the reaction solution to 45-70 DEG C, adding a mixed solution of diethylamine and waterto form a salt, cooling and crystallizing, so as to obtain the etamsylate. According to the reaction system used in the method, the fluidity of the system is improved, and the three-transfer-one-reaction efficiency is improved, so that the conversion rate of the materials is improved by 5-10%; when the system is cooled to 45-70 DEG C after the reaction is ended, the mixed solution of diethylamineand water is directly added into the system, the operation is simplified, and the after-treatment time is shortened; concentrated water is avoided, the energy consumption is reduced, and the yield ofthe product after salt formation reaches 80-85%; the product does not need to be re-crystallized or subjected to activated carbon discoloration, the purity directly reaches 99.5% or higher, and the content of all single impurities is lower than 0.05%; in addition, the use of a type of solvents and reagents containing genotoxicity warning structures is avoided, and totally safe and low-toxicity class-2 and class-3 solvents friendly to the humans and environment are used.

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