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251682

Sigma-Aldrich

Sodium 3-mercapto-1-propanesulfonate

technical grade, 90%

Synonym(s):

3-Mercapto-1-propanesulfonic acid sodium salt, MPS

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About This Item

Linear Formula:
HSCH2CH2CH2SO3Na
CAS Number:
Molecular Weight:
178.21
Beilstein:
5362242
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

technical grade

Assay

90%

form

powder

mp

~220 °C (dec.) (lit.)

solubility

water: soluble 50 mg/mL, colorless

functional group

sulfonic acid

SMILES string

[Na+].[O-]S(=O)(=O)CCCS

InChI

1S/C3H8O3S2.Na/c4-8(5,6)3-1-2-7;/h7H,1-3H2,(H,4,5,6);/q;+1/p-1

InChI key

FRTIVUOKBXDGPD-UHFFFAOYSA-M

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General description

Sodium 3-mercapto-1-propanesulfonate forms self assembled monolayer via chemisorption on a gold-coated substrate.

Application

Sodium 3-mercapto-1-propanesulfonate (MPS) can be used to prepare tetrasubstituted organosilicon thioether by photochemical reaction with tetravinylsilane via thiol-ene reaction. It can also be used as a capping agent to functionalize gold nanoparticles for potential applications in the field of radiotherapy and drug delivery.
MPS can be also used in the preparation of Rh nanoparticles by liquid-phase reduction of rhodium (III) chloride.

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

Flash Point(F)

159.8 °F - closed cup

Flash Point(C)

71 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Sakamoto N, et al.
Nanoscale, 1(1), 106-109 (2009)
Synthesis of functionalized gold nanoparticles capped with 3-mercapto-1-propansulfonate and 1-thioglucose mixed thiols and ?in vitro? bioresponse
Porcaro F, et al.
Colloids and Surfaces. B, Biointerfaces, 142(20), 408-416 (2016)
Thiol- Ene Reaction for the Synthesis of Multifunctional Branched Organosilanes
Rissing C and Son DY
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