251682
Sodium 3-mercapto-1-propanesulfonate
technical grade, 90%
Synonyme(s) :
3-Mercapto-1-propanesulfonic acid sodium salt, MPS
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A propos de cet article
Formule linéaire :
HSCH2CH2CH2SO3Na
Numéro CAS:
Poids moléculaire :
178.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
241-620-3
Beilstein/REAXYS Number:
5362242
MDL number:
Assay:
90%
Form:
powder
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technical grade
Quality Level
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
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.
MPS can be also used in the preparation of Rh nanoparticles by liquid-phase reduction of rhodium (III) chloride.
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Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Classe de stockage
11 - Combustible Solids
wgk
WGK 1
flash_point_f
159.8 °F - closed cup
flash_point_c
71 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
Organometallics, 27(20), 5394-5397 (2008)
Geoffrey J Ashwell et al.
Faraday discussions, 131, 23-31 (2006-03-04)
The chevron-shaped dye, N-butyl-2,6-bis-[2-{4-(2-(4-dibutylaminophenyl)-vinyl)-phenyl}-vinyl]-pyridinium iodide, has a hydrophilic apex that is electron-accepting and hydrophobic it-bridged limbs that are electron-donating. It forms non-centrosymmetric monolayers at the air-water interface and when deposited, its LB films exhibit second-harmonic generation and asymmetric current-voltage (I-V)