MES monohydrate - ≥99%(T) , CAS No.145224-94-8

CAS: 145224-94-8 Cat. No.: M105074 Fórmula: C₆H₁₃NO₄S·H₂O Peso molecular: 213.25 Beilstein Registry Number: 6350956 Número EC: 630-505-7

CALIDAD & PUREZA ≥99%(T)

Synonyms

MES monohydrate|2-(N-Morpholino)ethanesulfonic acid hydrate|2-morpholin-4-ylethanesulfonic acid;hydrate|3,3-difluoro-cyclobutane-1-carboxylic acid|2-(n-morpholino)ethanesulfonic acid monohydrate|2-Morpholinoethanesulfonic acid hydrate|2-(morpholin-4-yl)ethane-1-sulfonic acid hydrate|4-Morpholineethanesulfonic acid, monohydrate|MES hydrate|2-morpholinoethanesulfonic acid monohydrate|4-Morpholineethanesulfonic acid, hydrate (1:1)|4-morpholineethanesulphonic acid-monohydrate|4-Morpholineethanesulfonic acid monohydrate|4-Morpholinoethanesulfonic acid hydrate|2-Morpholinoethane-1-sulfonic acid hydrate|2,5-METHANO-2H-INDENO(1,2-B)OXIRENE, 2,3,4,5,6,6A,7,7-OCTACHLORO-1A,1B,5,5A,6,6A-HEXAHYDRO-, (1A.ALPHA.,1B.BETA.,2.ALPHA.,5.ALPHA.,5A.BETA.,6.BETA.,6A.ALPHA.)-|2-(4-Morpholino)ethanesulfonic acid hydrate|2-Morpholin-4-yl-ethanesulfonic acid hydrate|2-(Morpholin-4-yl)ethane-1-sulfonic acid--water (1/1)|4-morpholineethanesulphonic acid monohydrate|2-Morpholinoethanesulfonic acid xhydrate

Storage

Room temperature

Shipped In

Normal

Descripción general

A zwitterionic N-substituted aminosulfonic acid Good’s buffer. Used as a running buffer for resolving very small proteins (ex: 13 kDa) on bis-tris gels; also used as a biological buffer in plant cell cultures.
Often used as a running buffer for resolving very small proteins.

MES monohydrate is a biological buffer often referred to as GoodÂ’s buffer. It is useful for cell culture media and protein based buffer formulations to maintain a stable environment in solution. It is also used in the purification bioprocesses of antibodies, peptides, proteins, blood components and growth factors. It is a useful resolving agent for very small proteins on bis-tris gels. Buffer solutions are used as a means of keeping pH at a nearly constant value in a wide variety of chemical applications.

Especificaciones

Sinónimos

MES monohydrate | 2-(N-Morpholino)ethanesulfonic acid hydrate | 2-morpholin-4-ylethanesulfonic acid;hydrate | 3,3-difluoro-cyclobutane-1-carboxylic acid | 2-(n-morpholino)ethanesulfonic acid monohydrate | 2-Morpholinoethanesulfonic acid hydrate | 2-(morpholin-4-yl)ethane-1-sulfonic acid hydrate | 4-Morpholineethanesulfonic acid, monohydra Show more

Especificaciones y pureza

≥99%(T)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥99%(T)

Nombres e identificadores

Pubchem Sid

504768341

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504768341

Sonrisas canónicas

C1COCCN1CCS(=O)(=O)O.O

IUPAC Name

2-morpholin-4-ylethanesulfonic acid;hydrate

InChIKey

MIIIXQJBDGSIKL-UHFFFAOYSA-N

INCHI

1S/C6H13NO4S.H2O/c8-12(9,10)6-3-7-1-4-11-5-2-7;/h1-6H2,(H,8,9,10);1H2

Isómeros SMILES

C1COCCN1CCS(=O)(=O)O.O

WGK Alemania

3

CAS alternativo

1266615-59-1

Peso molecular

213.25

Beilstein

6350956

Reaxy-Rn

6350956

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6350956&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: 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
• Descripción: 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: Not available

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

Propiedades químicas y físicas

• Solubilidad: Soluble in water (0.5 M at 20 °C).
• Punto de fusión (°C): ca 308° dec.
• Peso molecular: 213.250 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• Exact Mass: 213.067 Da
• Monoisotopic Mass: 213.067 Da
• Topological Polar Surface Area: 76.200 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 214.000
• 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: 2

XLogP3