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2-(Dimethylamino)ethanesulfonic acid, also known as taurine, is a beta-amino sulfonic acid compound with the chemical formula C4H11NO3S. It is widely present in many animal tissues and some plants, playing a significant role in various physiological processes, particularly in the central nervous system, where it functions as a neurotransmitter and neuromodulator. Taurine also possesses antioxidant properties and is involved in the regulation of electrolyte balance and cardiovascular function.

637-95-6

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637-95-6 Usage

Uses

Used in Dietary Supplements and Energy Drinks:
2-(Dimethylamino)ethanesulfonic acid is used as a dietary supplement and energy drink ingredient for its potential health benefits. It helps improve physical performance, cognitive function, and overall well-being.
Used in Pharmaceutical Products:
In the pharmaceutical industry, 2-(Dimethylamino)ethanesulfonic acid is used as an active ingredient in some medications due to its various physiological effects, such as its role in the central nervous system and its antioxidant properties.
Used in Research and Development:
2-(Dimethylamino)ethanesulfonic acid is utilized in research and development for its potential applications in various fields, including neuroscience, cardiovascular health, and antioxidant therapies. Its unique properties make it a valuable compound for scientific exploration and innovation.

Check Digit Verification of cas no

The CAS Registry Mumber 637-95-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 637-95:
(5*6)+(4*3)+(3*7)+(2*9)+(1*5)=86
86 % 10 = 6
So 637-95-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H11NO3S/c1-5(2)3-4-9(6,7)8/h3-4H2,1-2H3,(H,6,7,8)

637-95-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(dimethylamino)ethanesulfonic acid

1.2 Other means of identification

Product number -
Other names 2-dimethylaminoethanesulfonic 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:637-95-6 SDS

637-95-6Downstream Products

637-95-6Relevant academic research and scientific papers

Potentiation of mitochondrial Ca2+ sequestration by taurine

Palmi, Mitri,Youmbi, Gisele Tchuisseu,Fusi, Fabio,Sgaragli, Gian P.,Dixon, Henry B.F.,Frosini, Maria,Tipton, Keith F.

, p. 1123 - 1131 (1999)

The effects of taurine (2-aminoethanesulphonic acid) and its analogues, 2-aminoethylarsonic acid, 2-hydroxyethanesulphonic (isethionic) acid, 3-aminopropanesulphonic acid, 2-aminoethylphosphonic acid, and N,N-dimethyltaurine, were studied on the transport of Ca2+ by mitochondria isolated from rat liver. Taurine enhanced Ca2+ uptake in an apparently saturable process, with a K(m) value of about 2.63 mM. Taurine behaved as an uncompetitive activator of Ca2+ uptake, increasing both the apparent K(m) and V(max) values of the process. This effect was not modified in the presence of cyclosporin A (CsA). N,N-Dimethyltaurine also stimulated Ca2+ uptake at higher concentrations, but there was no evidence that the process was saturable over the concentration range used (1-10 mM). Aminoethylarsonate was a weak inhibitor of basal Ca2+ uptake, but inhibited that stimulated by taurine in an apparently competitive fashion (K(i) = 0.05 mM). The other analogues had no significant effects on this process. Taurine either in the presence or the absence of CsA had no effect on Ca2+ release induced by 200 nM ruthenium red. Thus, the mechanism of taurine-enhanced Ca2+ accumulation appears to involve stimulation of Ca2+ uptake via the uniport system rather than inhibition of Ca2+ release via the ion (Na+/Ca2+ and/or H+/Ca2+) exchangers or by taurine modulating the permeability transition of the mitochondrial inner membrane. Overall, these findings indicate an interaction of taurine with an as yet unidentified mitochondrial site which might regulate the activity of the uniporter. The unique role of taurine in modulating mitochondrial Ca2+ homeostasis might be of particular importance under pathological conditions that are characterised by cell Ca2+ overload, such as ischaemia and oxidative stress. Copyright (C) 1999 Elsevier Science Inc.

Covalently Bonded Polymeric Zwitterionic Stationary Phase for Simultaneous Separation of Inorganic Cations and Anions

Jiang, Wen,Irgum, Knut

, p. 333 - 344 (1999)

A novel polymer-based zwitterionic separation material was synthesized by a two-step reaction, in which 2-hydroxyethyl methacrylate-ethylene dimethacrylate copolymer beads were first activated with epichlorohydrin, whereafter (2-dimethylamino)ethanesulfonic acid inner salt was coupled to the epoxide groups on the activated beads in a quaternizing reaction. The resulting material carried strong/strong charge zwitterionic pendant groups, whose charge properties did not change over a wide pH range. It was capable of separating inorganic anions and cations both independently and simultaneously using aqueous solutions of perchloric acid or perchlorate salts as eluent It was found that the retention of cations and anions depended on the individual ions in the analyte, not on type of salt injected, as reported for ODS columns dynamically coated with zwitterionic detergents using water only as eluent. This study also revealed that both the concentration and the water structure related properties of the eluent ions were important for the retention of ionic species. The mechanism appears to involve the interaction of the chaotropic anion component with the quaternary ammonium group, resulting in an increasing cation-exchange capacity of the zwitterion up to a perchloric add eluent concentration of c.a. 10 mM. Above this concentration the material appears to become saturated, and the retention times of both cations and anions become practically independent of the HClO4 concentration.

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