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Contents

   



(Top)
 


1 Applications  





2 See also  





3 References  





4 External links  














MOPS






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From Wikipedia, the free encyclopedia
 


MOPS
Names
Preferred IUPAC name

3-(Morpholin-4-yl)propane-1-sulfonic acid

Other names

3-(N-Morpholino)propanesulfonic acid,
3-Morpholinopropanesulfonic acid,
3-N-Morpholino propansulfonic acid,
4-Morpholinepropanesulfonic acid

Identifiers

CAS Number

3D model (JSmol)

ChemSpider
ECHA InfoCard 100.013.162 Edit this at Wikidata

PubChem CID

  • 2723950
  • UNII

    CompTox Dashboard (EPA)

    • InChI=1S/C7H15NO4S/c9-13(10,11)7-1-2-8-3-5-12-6-4-8/h1-7H2,(H,9,10,11) ☒N

      Key: DVLFYONBTKHTER-UHFFFAOYSA-N ☒N

    • InChI=1/C7H15NO4S/c9-13(10,11)7-1-2-8-3-5-12-6-4-8/h1-7H2,(H,9,10,11)

      Key: DVLFYONBTKHTER-UHFFFAOYAN

    • C1COCCN1CCCS(=O)(=O)O

    Properties

    Chemical formula

    C7H15NO4S
    Molar mass 209.26 g·mol−1
    Hazards
    GHS labelling:

    Pictograms

    GHS07: Exclamation mark

    Signal word

    Warning

    Hazard statements

    H315, H319, H335

    Precautionary statements

    P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
    Safety data sheet (SDS) MSDS

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    MOPS (3-(N-morpholino)propanesulfonic acid) is a buffer introduced in the 1960s, one of the twenty Good's buffers. It is a structural analog to MES,[1] and like MES, its structure contains a morpholine ring. HEPES is a similar pH buffering compound that contains a piperazine ring. With a pKa of 7.20, MOPS is an excellent buffer for many biological systems at near-neutral pH.

    Applications[edit]

    MOPS is frequently used as a buffering agentinbiology and biochemistry. It has been tested and recommended for polyacrylamide gel electrophoresis.[2] Usage above 20 mM in mammalian cell culture work is not recommended.[3] MOPS buffer solutions become discolored (yellow) over time, but reportedly slight discoloration does not significantly affect the buffering characteristics.[4]

    See also[edit]

    References[edit]

    1. ^ Good, Norman E.; Winget, G. Douglas; Winter, Wilhelmina; Connolly, Thomas N.; Izawa, Seikichi; Singh, Raizada M. M. (1966). "Hydrogen Ion Buffers for Biological Research". Biochemistry. 5 (2): 467–77. doi:10.1021/bi00866a011. PMID 5942950.
  • ^ Thomas, J; Hodes, ME (1981). "A new discontinuous buffer system for the electrophoresis of cationic proteins at near-neutral pH". Analytical Biochemistry. 118 (1): 194–6. doi:10.1016/0003-2697(81)90178-0. PMID 6278979.
  • ^ Eagle, H. (1971). "Buffer Combinations for Mammalian Cell Culture". Science. 174 (4008): 500–3. Bibcode:1971Sci...174..500E. doi:10.1126/science.174.4008.500. PMID 5110427. S2CID 29876583.
  • ^ https://bostonbioproducts.com/products/mops-buffer-1-m-ph-74-bbm-74. {{cite web}}: Missing or empty |title= (help)
  • External links[edit]


    Retrieved from "https://en.wikipedia.org/w/index.php?title=MOPS&oldid=1164683225"

    Categories: 
    Buffer solutions
    Sulfonic acids
    4-Morpholinyl compounds
    Hidden categories: 
    CS1 errors: missing title
    CS1 errors: bare URL
    Chemical articles with multiple compound IDs
    Multiple chemicals in an infobox that need indexing
    Chemical articles with multiple PubChem CIDs
    Articles without EBI source
    Articles without KEGG source
    Articles with changed ChemSpider identifier
    ECHA InfoCard ID from Wikidata
    Articles with changed InChI identifier
    Chembox having GHS data
    Articles containing unverified chemical infoboxes
    Articles with short description
    Short description matches Wikidata
     



    This page was last edited on 10 July 2023, at 13:19 (UTC).

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