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Tris(2-hydroxyethyl)ammonium hydrogen maleate, also known as T2EAHM, is a complex organic compound with the chemical formula C10H21NO6. It is a derivative of tris(2-hydroxyethyl)amine (T2EA), where one of the hydroxyl groups is replaced by a maleate ion (C4H3O4-). tris(2-hydroxyethyl)ammonium hydrogen maleate is a zwitterionic surfactant, meaning it has both positive and negative charges, which can be useful in various applications such as emulsification, solubilization, and stabilization of colloidal systems. T2EAHM is also known for its potential use in drug delivery systems and as a building block for more complex molecules in chemical synthesis. Its amphoteric nature allows it to interact with a wide range of substances, making it a versatile component in various chemical and pharmaceutical processes.

41397-50-6

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41397-50-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41397-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,9 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 41397-50:
(7*4)+(6*1)+(5*3)+(4*9)+(3*7)+(2*5)+(1*0)=116
116 % 10 = 6
So 41397-50-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H15NO3.C4H4O4/c8-4-1-7(2-5-9)3-6-10;5-3(6)1-2-4(7)8/h8-10H,1-6H2;1-2H,(H,5,6)(H,7,8)/b;2-1-

41397-50-6SDS

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 Ethanaminium, 2-hydroxy-N,N-bis(2-hydroxyethyl)- (2Z)-2-butenedio ate (1:1)

1.2 Other means of identification

Product number -
Other names -

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:41397-50-6 SDS

41397-50-6Downstream Products

41397-50-6Relevant academic research and scientific papers

Reactions of 1-Germatranol Hydrate with Dicarboxylic Acids

Baryshok, V. P.,Le, G. N. T.

, p. 2430 - 2440 (2022/01/22)

Abstract: The reactions of 1-germatranol hydrate with malonic, succinic, maleic, cork, sebacic acids, and bistrimethylsilyl ester of succinic acid, and also of bis(germatran-1-yl)oxane with succinic acid in acetonitrile, water, methanol, and dimethylsulfoxide were studied. In organic solvents, mono- and dicarboxyl-substituted 1-germatranols are formed, which, like 1-germatranol, are reversibly hydrolyzed with water in an acidic medium. Removing water from reaction mixtures due to evaporation and a topochemical reaction increases the yield of esterified 1-germatranol.

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