MOPS - ≥99.5%(T) , CAS No.1132-61-2

CAS: 1132-61-2 Cat. No.: M105135 Summenformel: C₇H₁₅NO₄S Molekulargewicht: 209.26 Beilstein Registry Number: 1106776 EG-Nummer: 214-478-5

GRADE & PURITY ≥99.5%(T)

Synonyms

4-Morpholinepropanesulfonic acid | BBL010801 | MOPS | NCGC00255922-01 | Q4030654 | 3-Morpholinopropane-1-sulfonic acid | 3-(morpholin-4-yl)propane-1-sulfonic acid (MOPS) | MFCD11100867 | MOPS, BioUltra, for molecular biology, >=99.5% (T) | MOPS, BioXtra,

Storage

Room temperature

Shipped In

Normal

Übersicht

useful pH range 6.5 - 7.9 pKa (25 °C) 7.2 3-(N-Morpholino)propane sulfonic acid (MOPS) is an N-substituted amino sulfonic acid with a morpholinic ring. MOPS is capable of buffering within a pH range of 6.5-7.9. MOPS is widely used in biological and biochemical studies due to its inert properties.It does not interact with any metal ions in solutions and has significant metal-buffer stability especially with copper (Cu), nickel (Ni), manganese (Mn), zinc (Zn), cobalt (Co) ions. MOPS buffer maintains the pH of the mammalian cell culture medium. MOPS functions to maintain pH in denaturing gel electrophoresis of RNA. MOPS can modify lipid interactions and influence the thickness and barrier properties of membranes. MOPS interacts with bovine serum albumin and stabilizes the protein. Hydrogen peroxide oxidizes MOPS slowly to N-oxide form
Good's buffer component for biological research Satisfactory for electron transport studies and phosphorylation in chloroplast lamella preparations; non-toxic buffering system for the extensive growth of Streptomyces clavuligerus and cephalosporin production, in a chemically defined medium; electrolyte system component for the IEF of 2-D gel electrophoresis

Specifications

Synonyme

4-Morpholinepropanesulfonic acid | BBL010801 | MOPS | NCGC00255922-01 | Q4030654 | 3-Morpholinopropane-1-sulfonic acid | 3-(morpholin-4-yl)propane-1-sulfonic acid (MOPS) | MFCD11100867 | MOPS, BioUltra, for molecular biology, >=99.5% (T) | MOPS, BioXtra,

Spezifikationen & Reinheit

≥99.5%(T)

Storage

Room temperature

Verschickt in

Normal

Reinheit

≥99.5%(T)

Namen und Kennungen

Pubchem Sid

504754576

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504754576

Kanonisches Lächeln

C1COCCN1CCCS(=O)(=O)O

IUPAC Name

3-morpholin-4-ylpropane-1-sulfonic acid

InChIKey

DVLFYONBTKHTER-UHFFFAOYSA-N

INCHI

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

Isomere SMILES

C1COCCN1CCCS(=O)(=O)O

WGK Deutschland

1

RTECS

QE9104530

Molekulargewicht

209.26

Beilstein

1106776

Reaxy-Rn

1106776

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1106776&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Klasse Oxazinanes
      • Subclass Morpholines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Klasse: Oxazinanes
• Subclass: Morpholines
• Intermediate Tree Nodes: Not available
• Direct Parent: Morpholines
• Alternative Parents: Sulfonyls Organosulfonic acids Alkanesulfonic acids Trialkylamines Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Morpholine - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Alkanesulfonic acid - Tertiary amine - Tertiary aliphatic amine - Dialkyl ether - Ether - Oxacycle - Azacycle - Organopnictogen compound - Organic oxygen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Amine - Aliphatic heteromonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as morpholines. These are organic compounds containing a morpholine moiety, which consists of a six-member aliphatic saturated ring with the formula C4H9NO, where the oxygen and nitrogen atoms lie at positions 1 and 4, respectively.
• External Descriptors: an aliphatic sulfonate

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemische und physikalische Eigenschaften

• Löslichkeit: Soluble in water.
• Flammpunkt (°F): 116°C
• Flammpunkt (°C): 116°C
• Schmelzpunkt (°C): 277-282°C
• Molekulargewicht: 209.270 g/mol
• XLogP3: -3.100
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 209.072 Da
• Monoisotopic Mass: 209.072 Da
• Topological Polar Surface Area: 75.200 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 227.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1