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

CAS: 145224-94-8 Cat. No.: M105074 Formula: C₆H₁₃NO₄S·H₂O Peso molecolare: 213.25 Beilstein Registry Number: 6350956 Numero EC: 630-505-7

QUALITÀ & PUREZZA ≥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

Panoramica

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.

Specifiche

Sinonimi

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 Mostra altro

Specifiche e purezza

≥99%(T)

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normal

Purezza

≥99%(T)

Nomi e identificatori

Pubchem Sid

504768341

Pubchem Sid Url

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

Sorrisi canonici

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

Isomeri SMILES

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

WGK Germania

3

CAS alternativo

1266615-59-1

Peso molecolare

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
    • Classe Oxazinanes
      • Subclass Morpholines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: 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
• Descrizione: 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

Proprietà chimiche e fisiche

• Solubilità: Soluble in water (0.5 M at 20 °C).
• Punto di fusione (°C): ca 308° dec.
• Peso molecolare: 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

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