6898-84-6

Basic information

• Product Name: SODIUM 1-PROPANETHIOLATE
• Synonyms: SODIUM 1-PROPANETHIOLATE;1-PROPANETHIOL SODIUM SALT;sodium propanethiolate;Sodium1-propanethiolate95+%;Sodium propane-1-thiolate;Sodium propyl sulfide;Sodium 1-propanethiolate technical, >=95% (RT)
• CAS NO: 6898-84-6
• Molecular Formula: C₃H₇S*Na
• Molecular Weight: 98.14
• EINECS: 230-005-5
• Product Categories: Building Blocks;Chemical Synthesis;Organic Building Blocks;Sulfur Compounds;Thiol/Mercaptan Salts
• Mol File: 6898-84-6.mol
• Article Data: 4

Chemical Properties

• Appearance: White to pale gray/Solid
• Sensitive: Air & Moisture Sensitive
• CAS DataBase Reference: SODIUM 1-PROPANETHIOLATE(CAS DataBase Reference)
• NIST Chemistry Reference: SODIUM 1-PROPANETHIOLATE(6898-84-6)
• EPA Substance Registry System: SODIUM 1-PROPANETHIOLATE(6898-84-6)

Safety Data

• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-36/37/39-45
• RIDADR: UN 3263 8/PG 3
• WGK Germany: 3
• F: 1-10-13
• TSCA: Yes
• HazardClass: 4.3
• PackingGroup: III
• Hazardous Substances Data: 6898-84-6(Hazardous Substances Data)

Usage

General Description

Sodium 1-propanethiolate is a chemical compound that consists of sodium and 1-propanethiolate anion. It is a white to off-white solid that is soluble in water. It is commonly used as an intermediate in the synthesis of various organic compounds, as well as a reagent in organic chemistry reactions. SODIUM 1-PROPANETHIOLATE is also known for its use as a polymerization inhibitor in the production of certain polymers. Additionally, it has applications in the manufacturing of pharmaceuticals, agrochemicals, and fragrances. Overall, sodium 1-propanethiolate is a versatile chemical with various uses in the industry.

InChI:InChI=1/C3H8S.Na/c1-2-3-4;/h4H,2-3H2,1H3;/q;+1/p-1

Upstream product

• 111-47-7 propyl sulfide 
• 7664-41-7 ammonia 
• 629-19-6 Dipropyl disulfide 
• 1071-75-6 2-propyl-isothiourea; hydrobromide 
• 107-03-9 1-thiopropane 
• 60-29-7 diethyl ether 

Downstream Products

• 59969-91-4 tris-propylsulfanyl-methane 
• 629-19-6 Dipropyl disulfide 
• 69078-86-0 propyl-(1-propylsulfanyl-ethyl)-disulfane 
• 67170-02-9 N-(2-Amino-5-propylsulfanyl-phenyl)-butyramide 
• 113121-36-1 6-propylsulfanylpyridazin-3-amine 
• 103653-39-0 N,N'-bis-(toluene-4-sulfonyl)-propane-1-sulfinamidine 
• 263276-29-5 4-chloro-6-propylthio-pyrimidine 
• 131716-92-2 triethyl{p-(propylthio)phenyl}germane 
• 113827-87-5 1,2,4,5-tetrafluoro-3-(propylthio)benzene 
• 1365239-04-8 N-cyclopropyl-2-methyl-4-{8-[(2-methylpropyl)amino]-6-(propylsulfanyl)imidazo[1,2-b]pyridazin-3-yl}benzamide 
• 854696-81-4 2-propylsulfanylbenzonitrile 
• 855196-51-9 4-(propylthio)benzonitrile 
• 274693-26-4 [3aR-[3aα,4α,6α,(1R,2S),6aα]]-2-[6-[[[7-(2-(3,4-difluorophenyl)cyclopropyl)]amino-5-(propylthio)-3H-1,2,3-triazolo[4,5-d]pyrimidin-3-yl]tetrahydro-2,2-dimethyl-4H-cyclopenteno-1,3-dioxolan-4-yl]oxy]ethanol 
• 76697-38-6 1-propylsulfanyl-2-nitrobenzene 

Relevant articles and documents

Rhenium Tris(pyrazolyl)Borate Oxothiolate Complexes: Syntheses and Structures

Abstract: The rhenium complexes TpReOCl(StBu) (I), TpReO(StBu)2 (II), and TpReO(SnC3H7)2 (III) are synthesized using two methods by analogy to the known thiophenyl complexes. Complexes I–III having more electron-donating alkylthiolate ligands are characterized by IR and NMR spectroscopy. The structures of complexes I–III are determined by X-ray diffraction analysis (СIF files CCDC nos. 1892096 (I), 1892097 (II), and 1892098 (III)). The temperature dependence of the spectra of the bis(thiolate) complexes allows one to determine the activation energy for the hindered rotation about the Re–thiolate ligand bond. The by-product of the reaction of TpReOCl2 with NaS-tert-Bu, binuclear oxygen-bridged complex TpReIVCl(S-tert-Bu)O(S-tert-Bu)2ReIVTp, is isolated and structurally characterized (СIF file CCDC no. 1892099).

SELF-ASSEMBLED POLYHEDRAL MULTIMERIC CHEMICAL STRUCTURES

Self-assembled, closed and hollow chemical multimer structures having a dodecahedral morphology, composed of chemical monomers having a structurally symmetric core which posses a 5-fold rotational symmetry, are provided. Also provided are methods of creating such chemical monomers, methods of creating such chemical multimer structures and compositions comprising these chemical multimer structures. Also provided are uses of these chemical multimer structures in applications such as drug delivery, imaging, immunization, formation of plastic crystals and nanopaticle matrices and other medical and material science applications.