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Merck
모든 사진(1)

주요 문서

251682

Sigma-Aldrich

Sodium 3-mercapto-1-propanesulfonate

technical grade, 90%

동의어(들):

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 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Grade

technical grade

Quality Level

분석

90%

양식

powder

mp

~220 °C (dec.) (lit.)

solubility

water: soluble 50 mg/mL, colorless

작용기

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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일반 설명

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

애플리케이션

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.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

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

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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시험 성적서(COA)

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Highly dispersed rhodium nanoparticles (1.7 +/- 0.3 nm) prepared by a liquid-phase reduction method were loaded on a solid solution of GaN and ZnO without forming aggregates, achieving improved activity for visible-light-driven overall water splitting when the nanoparticles are coated
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
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