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3-[(2-AMINOETHYL)AMINO]PROPANESULFONIC ACID, commonly known as taurine, is an organic sulfur-containing amino acid that is extensively present in animal tissues. It is involved in a multitude of physiological functions such as bile salt synthesis, neurological function, and cardiovascular health. Taurine is recognized for its potential benefits in enhancing exercise performance, reducing muscle fatigue, and possesses antioxidant properties that may support eye health and insulin sensitivity. Although it is a non-essential amino acid that can be synthesized in the body, supplementation may be advantageous for individuals with specific health conditions or dietary limitations.

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  • 14235-54-2 Structure
  • Basic information

    1. Product Name: 3-[(2-AMINOETHYL)AMINO]PROPANESULFONIC ACID
    2. Synonyms: EPS;3-[(2-AMINOETHYL)AMINO]PROPANESULFONIC ACID;3-((2-AMinoethyl)aMino)propane-1-sulfonic acid;Flame Retardant Grade Expandable Polystyrene
    3. CAS NO:14235-54-2
    4. Molecular Formula: C5H14N2O3S
    5. Molecular Weight: 182.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 14235-54-2.mol
  • Chemical Properties

    1. Melting Point: 215 °C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.282 g/cm3
    6. Refractive Index: 1.514
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 1.45±0.50(Predicted)
    10. CAS DataBase Reference: 3-[(2-AMINOETHYL)AMINO]PROPANESULFONIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-[(2-AMINOETHYL)AMINO]PROPANESULFONIC ACID(14235-54-2)
    12. EPA Substance Registry System: 3-[(2-AMINOETHYL)AMINO]PROPANESULFONIC ACID(14235-54-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 14235-54-2(Hazardous Substances Data)

14235-54-2 Usage

Uses

Used in Sports Nutrition:
3-[(2-AMINOETHYL)AMINO]PROPANESULFONIC ACID is used as a performance enhancer in sports nutrition for its potential to improve exercise performance and reduce muscle fatigue, making it a popular ingredient in energy drinks and supplements.
Used in Antioxidant Formulations:
In the health and wellness industry, 3-[(2-AMINOETHYL)AMINO]PROPANESULFONIC ACID is used as an antioxidant for its ability to combat oxidative stress, which may contribute to the maintenance of overall health and potentially support eye health.
Used in Pharmaceutical Applications:
3-[(2-AMINOETHYL)AMINO]PROPANESULFONIC ACID is utilized as a therapeutic agent in pharmaceuticals for its potential role in supporting cardiovascular health and managing certain health conditions that may benefit from its unique properties.
Used in Dietary Supplements:
In the dietary supplement industry, 3-[(2-AMINOETHYL)AMINO]PROPANESULFONIC ACID is used as a supplement for individuals who may have increased needs due to their health conditions or dietary restrictions, helping to ensure adequate intake of this amino acid.

Check Digit Verification of cas no

The CAS Registry Mumber 14235-54-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,3 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14235-54:
(7*1)+(6*4)+(5*2)+(4*3)+(3*5)+(2*5)+(1*4)=82
82 % 10 = 2
So 14235-54-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H14N2O3S/c6-2-4-7-3-1-5-11(8,9)10/h7H,1-6H2,(H,8,9,10)

14235-54-2SDS

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 3-(2-aminoethylamino)propane-1-sulfonic acid

1.2 Other means of identification

Product number -
Other names I05-0488

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:14235-54-2 SDS

14235-54-2Downstream Products

14235-54-2Relevant articles and documents

Preparation method of double-terminal amino type hydrophilic chain extender

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Paragraph 0013; 0028-0031; 0033-0036; 0039-0042; 0045-0048, (2021/07/21)

The invention discloses a preparation method of a double-terminal amino type hydrophilic chain extender. The method comprises the following steps: dissolving ethylenediamine in a solvent, dispersing, controlling the temperature of a system, dropwise adding 1, 3-propane sultone into the system, controlling the dropwise adding speed, keeping the temperature of the system, controlling the dropwise adding time to be 2-4 hours, and controlling the later aging time to be 2-5 hours; after a secondary amine value and a total amine value of a sample are monitored through central control sampling, adding alkali to carry out an acid-base reaction on a sulfonic acid part of the sample, regulating the pH to a proper range, removing a solvent existing in a system under reduced pressure, and finally adding water to adjust the solid content to a proper range, so that a double-terminal amino type hydrophilic chain extender aqueous solution can be obtained. The invention provides a preparation method of a double-terminal amino type hydrophilic chain extender similar to ethylenediamine esilate in structure and property; wherein the ring-opening reaction and selectivity of 1,3-propane sultone are utilized, and selective synthesis is carried out in an aqueous solution; the synthesis process is simple, a large number of organic solvents are not needed, a complicated post-treatment process is not needed, the preparation method is green and environment-friendly, and the industrialization degree is high.

Amino-phosphonic-sulfonic acids

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, (2008/06/13)

This invention relates to compounds characterized by the presence of N-methyl, or substituted methyl, phosphonic acid and N-propylenesulfonic acid groups. These compounds contain at least one or more of each group and are bonded to the same or different amino groups. They are derived by reacting an amine with both propane sultone and with a carbonyl compound, such as formaldehyde, and phosphorous acid or its equivalent. They have a wide variety of uses, for example as scale and corrosion inhibitors, chelating agents, etc.

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