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Merck
CN

63765

3-巯基-1-丙磺酸钠

technical, ~80% (RT)

别名:

3-巯基-1-丙烷磺酸 钠盐, MPS

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关于此项目

线性分子式:
HSCH2CH2CH2SO3Na
化学文摘社编号:
分子量:
178.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
241-620-3
Beilstein/REAXYS Number:
5362242
MDL number:
Assay:
~80% (RT)
Form:
solid
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InChI key

FRTIVUOKBXDGPD-UHFFFAOYSA-M

InChI

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

SMILES string

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

grade

technical

assay

~80% (RT)

form

solid

mp

~220 °C (dec.) (lit.)

Quality Level

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Application

Sodium 3-mercapto-1-propanesulfonate can also be involved in the synthesis of rhodium nanoparticles via liquid phase reduction method.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

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

法规信息

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Elsa G Shapiro et al.
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"Highly dispersed noble-metal/chromia (core/shell) nanoparticles as efficient hydrogen evolution promoters for photocatalytic overall water splitting under visible light"
Sakamoto N, et al.
Nanoscale, 1(01), 106- 109 (2009)
Brener R C Vale et al.
Scientific reports, 9(1), 8332-8332 (2019-06-07)
CdTe/CdS core/shell quantum dots (QDs) are formed in aqueous synthesis via the partial decomposition of hydrophilic thiols, used as surface ligands. In this work, we investigate the influence of the chemical nature (functional group and chain length) of the used
Matilda Jackson et al.
Molecular genetics and metabolism, 114(4), 584-593 (2015-03-10)
Mucopolysaccharidoses (MPS) are inherited metabolic disorders that arise from a complete loss or a reduction in one of eleven specific lysosomal enzymes. MPS children display pathology in multiple cell types leading to tissue and organ failure and early death. Mesenchymal
S Q Wong et al.
British journal of cancer, 112(8), 1411-1420 (2015-03-06)
Recent discoveries in cancer research have revealed a plethora of clinically actionable mutations that provide therapeutic, prognostic and predictive benefit to patients. The feasibility of screening mutations as part of the routine clinical care of patients remains relatively unexplored as

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