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68399-77-9

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68399-77-9 Usage

Chemical Properties

white crystalline powder

Uses

Different sources of media describe the Uses of 68399-77-9 differently. You can refer to the following data:
1. MOPSO is a buffer that works in the 6-7 pH range. Used in pharmaceutical synthesis.
2. MOPSO is a biological buffer also referred to as a second generation “Good′s” buffer which displays improved solubility compared to traditional “Good′s” buffers. The pKa of MOPSO is 6.9 which make it an ideal candidate for buffer formulations which require a pH slightly below physiological to maintain a stable environment in solution. MOPSO is considered to be non-toxic to culture cell lines and provides high-solution clarity.MOPSO can be used in cell culture media, biopharmaceutical buffer formulations (both upstream and downstream) and diagnostic reagents.

Check Digit Verification of cas no

The CAS Registry Mumber 68399-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,9 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68399-77:
(7*6)+(6*8)+(5*3)+(4*9)+(3*9)+(2*7)+(1*7)=189
189 % 10 = 9
So 68399-77-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NO5S/c9-7(6-14(10,11)12)5-8-1-3-13-4-2-8/h7,9H,1-6H2,(H,10,11,12)/t7-/m1/s1

68399-77-9 Well-known Company Product Price

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  • (Code)Product description
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  • TCI America

  • (H0671)  2-Hydroxy-3-morpholinopropanesulfonic Acid  >98.0%(T)

  • 68399-77-9

  • 25g

  • 160.00CNY

  • Detail
  • Alfa Aesar

  • (44135)  MOPSO, 98%   

  • 68399-77-9

  • 10g

  • 71.0CNY

  • Detail
  • Alfa Aesar

  • (44135)  MOPSO, 98%   

  • 68399-77-9

  • 50g

  • 272.0CNY

  • Detail
  • Alfa Aesar

  • (44135)  MOPSO, 98%   

  • 68399-77-9

  • 250g

  • 1360.0CNY

  • Detail
  • Alfa Aesar

  • (44135)  MOPSO, 98%   

  • 68399-77-9

  • 1kg

  • 5441.0CNY

  • Detail

68399-77-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-3-morpholin-4-ylpropane-1-sulfonic acid

1.2 Other means of identification

Product number -
Other names 2-Hydroxy-3-morpholinopropanesulfonic acid,Free 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:68399-77-9 SDS

68399-77-9Downstream Products

68399-77-9Relevant articles and documents

Method for synthesizing 3 - (N - morpholinyl) -2 - hydroxyl propanesulfonic acid without solvent

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Paragraph 0025-0055, (2021/11/10)

The invention relates to a method for synthesizing 3 - (N - morpholinyl) -2 - hydroxyl propanesulfonic acid without a solvent, and belongs to the technical field of organic synthesis. To the method, morpholine and 3 -chloro -2 -hydroxypropanesulfonate are adopted, the reaction is conducted under the condition of no solvent, and 3 - (N - morpholinyl) -2 - hydroxypropanesulfonic acid is obtained after the reaction is finished. Compared with the original 3 - (N - morpholinyl) -2 - hydroxypropanesulfonic acid production process, the raw materials are easily available, the operation is simple, the process yield is high and stable, and the product quality is excellent. The problems that the yield is low and the process is complex in the prior art are solved.

3-(N-morpholine)-2-hydroxyl propanesulfonic acid synthesizing technology

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Paragraph 0011; 0012; 0013; 0014, (2017/04/28)

The invention relates to a 3-(N-morpholine)-2-hydroxyl propanesulfonic acid synthesizing technology, and discloses a preparation method of a N-substituted morpholine organic compound. The preparation method comprises the following steps that cyclodehydration is conducted to obtain morpholine, neutralizing, filtering, rectifying and synthesizing are conducted to obtain 3-(N-morpholine)-2-hydroxyl propanesulfonic acid, and chromatography and purification are conducted to obtain the final product. According to the method, reaction conditions are mild, operation is easy and convenient, the safety is high, industrialization is easy to achieve, and the yield is stably 95% or above; in addition, reagents are low in cost and easy to obtain, and therefore obvious cost and technique advantages are achieved.

Amino-hydroxy-alkyl sulfonic acid zwitterions

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, (2008/06/13)

Novel amino-hydroxy-alkylene sulfonic acid zwitterions are described which have the general formulas STR1 wherein A and B are each independently a hydrogen atom, an aliphatic, cycloaliphatic or hydroxyaliphatic group, N is one or two, and R=n is a cyclic radical comprising one or two ring nitrogen atoms, zero or one ring oxygen atoms and the remainder of the ring being carbon atoms, and water soluble salts of said acids. These organo-sulfonic acid compounds are useful as hydrogen ion buffers in biological research and particularly for tissue culture.

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