Skip to Content
Merck
CN

M8389

Sigma-Aldrich

MOPSO

≥99% (titration)

Synonym(s):

β-Hydroxy-4-morpholinepropanesulfonic acid, 3-Morpholino-2-hydroxypropanesulfonic acid

Sign Into View Organizational & Contract Pricing

Select a Size

25 MG
CN¥731.62
100 MG
CN¥915.91
500 MG
CN¥2,452.61
1 G
CN¥4,272.88

CN¥731.62


In StockDetails


Request a Bulk Order

Select a Size

Change View
25 MG
CN¥731.62
100 MG
CN¥915.91
500 MG
CN¥2,452.61
1 G
CN¥4,272.88

About This Item

Empirical Formula (Hill Notation):
C7H15NO5S
CAS Number:
Molecular Weight:
225.26
Beilstein:
1109697
EC Number:
MDL number:
UNSPSC Code:
12161700
PubChem Substance ID:
NACRES:
NA.25

CN¥731.62


In StockDetails


Request a Bulk Order

Quality Level

Assay

≥99% (titration)

form

crystalline powder

pH

6.2-7.6

useful pH range

6.2-7.6

pKa 

6.9

solubility

water: 0.333 mg/mL, clear, colorless

application(s)

diagnostic assay manufacturing

SMILES string

OC(CN1CCOCC1)CS(O)(=O)=O

InChI

1S/C7H15NO5S/c9-7(6-14(10,11)12)5-8-1-3-13-4-2-8/h7,9H,1-6H2,(H,10,11,12)

Looking for similar products? Visit Product Comparison Guide

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
P4279P3782P2772
assay

≥99% (TLC)

assay

≥99% (TLC)

assay

≥98%

assay

≥99%

functional group

phospholipid

functional group

phospholipid

functional group

-

functional group

phospholipid

biological source

egg yolk

biological source

egg yolk

biological source

soybean

biological source

egg yolk

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

form

lyophilized powder

form

solution

form

solution

form

solution

shipped in

ambient

shipped in

-

shipped in

-

shipped in

-

Caution

According to Ferreira, et al., MOPSO can have a strong interaction with iron in solution.[1] Based on this citation, it is recommended to use plastic-coated or PTFE-coated utensils when working with this chemical.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Lea M Hürlimann et al.
Antimicrobial agents and chemotherapy, 60(9), 5400-5411 (2016-07-07)
Nosocomial infections with Enterococcus faecalis are an emerging health problem. However, drug efflux pumps contributing to intrinsic drug resistance are poorly studied in this Gram-positive pathogen. In this study, we functionally investigated seven heterodimeric ABC transporters of E. faecalis that
FTIR-spectroscopic characterization of phosphocholine-headgroup model compounds
Pohle W, et al.
Journal of Molecular Structure, 563, 463-467 (2001)
Coactosin-like protein supports 5-lipoxygenase enzyme activity and up-regulates leukotriene A4 production
Rakonjac M, et al.
Proceedings of the National Academy of Sciences of the USA, 103(35), 13150-13155 (2006)
Molecular distinction of phosphatidylcholine synthesis between the CDP-choline pathway and phosphatidylethanolamine methylation pathway
DeLong CJ, et al.
The Journal of Biological Chemistry, 274(42), 29683-29688 (1999)
Chemical cross-linking provides a model of the gamma-secretase complex subunit architecture and evidence for close proximity of the C-terminal fragment of presenilin with APH-1
Steiner H, et al.
The Journal of Biological Chemistry, 283(50), 34677-34686 (2008)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service