HEPES(HEPES) - UltraBio™, Ultra pure, ≥99.5%(T), pH 5.0-6.5 (1 M in H2O) , CAS No.7365-45-9

CAS: 7365-45-9 Cat. No.: H433403 Formule: C₈H₁₈N₂O₄S Poids moléculaire: 238.30 Numéro CE: 230-907-9

QUALITÉ & PURETÉ UltraBio™, Ultra pure, ≥99.5%(T), pH 5.0-6.5 (1 M in H2O)

Synonyms

HEPES, BioXtra, pH 5.0-6.5 (1 M in H2O), >=99.5% (titration) | 1d1p | STK033062 | 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid | HEPES, biochemical grade | 4-(2-Hydroxyethyl)piperazine-1-(2-ethanesulfonic acid) | AMY23345 | DTXSID5040382 | Epit

Storage

Room temperature

Vue d’ensemble

HEPES has been described as one of the best all-purpose buffers available for biological research. At biological pH, the molecule is zwitterionic, and is effective as a buffer at pH 6.8 to 8.2. HEPES has been used in a wide variety of applications, including tissue culture. It is commonly used to buffer cell culture media in air. HEPES finds its usage in in vitro experiments on Mg.

Application

HEPES has been used: As a component of homogenisation buffer used in protein sample preparation To neutralise PRP (platelet-rich plasma) solution as part of PRP preparation As a component in 2X PBS buffer, which is used in phosphate calcium transfection in cell line preparation As a supplement in RPMI 1640 medium used to culture human umbilical vein endothelial cells (HUVEC) and in M199 complete medium for ex-vivo treatment of testicular tissue.

Other Notes

Easily compare specifications for HEPES products with the HEPES specification table .

Spécifications

Synonymes

HEPES, BioXtra, pH 5.0-6.5 (1 M in H2O), >=99.5% (titration) | 1d1p | STK033062 | 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid | HEPES, biochemical grade | 4-(2-Hydroxyethyl)piperazine-1-(2-ethanesulfonic acid) | AMY23345 | DTXSID5040382 | Epit

Spécifications et pureté

UltraBio™, Ultra pure, ≥99.5%(T), pH 5.0-6.5 (1 M in H2O)

Conditions de stockage de stockage

Room temperature

Grade

Ultra pure, UltraBio™

Pureté

≥99.5%(T)

Noms et identifiants

Sourires canoniques

C1CN(CCN1CCO)CCS(=O)(=O)O

IUPAC Name

2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid

InChIKey

JKMHFZQWWAIEOD-UHFFFAOYSA-N

INCHI

1S/C8H18N2O4S/c11-7-5-9-1-3-10(4-2-9)6-8-15(12,13)14/h11H,1-8H2,(H,12,13,14)

Isomères SMILES

C1CN(CCN1CCO)CCS(=O)(=O)O

RTECS

TL6809000

Poids moléculaire

238.30

Reaxy-Rn

883043

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=883043&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Diazinanes
      • Subclass Piperazines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Diazinanes
• Subclass: Piperazines
• Intermediate Tree Nodes: Not available
• Direct Parent: N-alkylpiperazines
• Alternative Parents: Sulfonyls Organosulfonic acids Alkanesulfonic acids Trialkylamines 1,2-aminoalcohols Azacyclic compounds Primary alcohols Organopnictogen compounds Organic zwitterions Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: N-alkylpiperazine - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Alkanesulfonic acid - 1,2-aminoalcohol - Tertiary amine - Tertiary aliphatic amine - Alkanolamine - Azacycle - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Primary alcohol - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Amine - Organic nitrogen compound - Alcohol - Organic zwitterion - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as n-alkylpiperazines. These are organic compounds containing a piperazine ring where the nitrogen ring atom carries an alkyl group.
• External Descriptors: organosulfonic acid - HEPES

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

Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: H2O: 1M, clear, colorless
• Point de fusion (°C): 210 °C
• Poids moléculaire: 238.310 g/mol
• XLogP3: -4.000
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 5
• Exact Mass: 238.099 Da
• Monoisotopic Mass: 238.099 Da
• Topological Polar Surface Area: 89.500 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 267.000
• 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