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RDD003

Sigma-Aldrich

MOPS

≥99.5%, crystalline powder, anhydrous, Redi-Dri™

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C7H15NO4S
CAS Number:
1132-61-2
Molecular Weight:
209.26
Beilstein:
1106776
EC Number:
214-478-5
MDL number:
MFCD00006183
UNSPSC Code:
12161700
PubChem Substance ID:
329824216
NACRES:
NA.25

product name

MOPS, anhydrous, free-flowing, Redi-Dri™, ≥99.5%

grade

anhydrous

product line

Redi-Dri™

Assay

≥99.5%

form

crystalline powder

quality

free-flowing

pH

2.5-4 (25 °C, 209 g/L)

useful pH range

6.5-7.9

pKa (25 °C)

7.2

solubility

water: 0.5 g/mL, clear, colorless

λ

33 % in H2O

SMILES string

OS(=O)(=O)CCCN1CCOCC1

InChI

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

InChI key

DVLFYONBTKHTER-UHFFFAOYSA-N

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Application


  • MOPS buffer for enhancing photoacoustic imaging: A study explored the utility of MOPS buffer in the synthesis of gold nanostars, enhancing their application in photoacoustic imaging due to the buffer′s pH stability, which is crucial for maintaining the optimal reaction conditions necessary for controlled nanostar growth (Zhang et al., 2024).

  • MOPS for intracytoplasmic sperm injection (ICSI): MOPS buffer′s role was investigated in a study where its influx following membrane piercing during ICSI was found to alter the transcriptome of human oocytes, suggesting a significant impact on oocyte viability and fertilization outcomes (Mendola et al., 2024).

  • Stability studies with MOPS in zinc complex formation: Utilizing MOPS buffer, a study examined the structures, solution equilibria, and speciation of zinc complexes with chloroquine and hydroxychloroquine, underlining the buffer′s role in maintaining the integrity and stability of these complexes (Squarcina et al., 2024).

  • MOPS in radiolabeling and in vivo evaluation: MOPS buffer was integral in the radiolabeling processes of lanmodulin with biomedically relevant lanthanide isotopes, enhancing the precision and effectiveness of in vivo evaluations in biomedical research (Martin et al., 2023).

Legal Information

Redi-Dri is a trademark of Sigma-Aldrich Co. LLC

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Certificates of Analysis (COA)

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Junji Suzuki et al.
Nature communications, 5, 4153-4153 (2014-06-14)
The endoplasmic reticulum (ER) and mitochondria accumulate Ca(2+) within their lumens to regulate numerous cell functions. However, determining the dynamics of intraorganellar Ca(2+) has proven to be difficult. Here we describe a family of genetically encoded Ca(2+) indicators, named calcium-measuring
Sanna Byström et al.
Journal of proteome research, 13(11), 4607-4619 (2014-09-19)
The brain is a vital organ and because it is well shielded from the outside environment, possibilities for noninvasive analysis are often limited. Instead, fluids taken from the spinal cord or circulatory system are preferred sources for the discovery of
Alexandre Albanese et al.
ACS nano, 8(6), 5515-5526 (2014-05-07)
A nanoparticle's physical and chemical properties at the time of cell contact will determine the ensuing cellular response. Aggregation and the formation of a protein corona in the extracellular environment will alter nanoparticle size, shape, and surface properties, giving it
Sewa Rijal et al.
Blood, 125(18), 2815-2824 (2015-03-05)
Phosphoinositide signaling regulates diverse cellular functions. Phosphoinositide-3 kinase (PI3K) generates PtdIns(3,4,5)P3 and PtdIns(3,4)P2, leading to the activation of proliferative and anti-apoptotic signaling pathways. Termination of phosphoinositide signaling requires hydrolysis of inositol ring phosphate groups through the actions of PtdIns(3,4,5)P3 3-phosphatase
Y S L Lee et al.
Human reproduction (Oxford, England), 30(3), 543-552 (2015-01-09)
What is the relationship between cleavage stage embryo kinetics, blastocyst metabolism and subsequent embryo viability? Embryos cleaving faster at the first cleavage division resulted in blastocysts with a larger inner cell mass (ICM), higher glucose consumption, lower glycolytic rate, higher
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