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Merck
CN

208043

Sodium sulfide nonahydrate

ACS reagent, ≥98.0%

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About This Item

Linear Formula:
Na2S·9H2O
CAS Number:
Molecular Weight:
240.18
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
215-211-5
MDL number:
Assay:
≥98.0%
Grade:
ACS reagent
Form:
crystals or chunks
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grade

ACS reagent

Quality Level

assay

≥98.0%

form

crystals or chunks

reaction suitability

reagent type: catalyst
core: sodium

color

colorless to slightly yellow

anion traces

SO32- and S2O32-: ≤0.1%

cation traces

Fe:, passes test, NH4+: ≤0.005%

storage temp.

2-8°C

SMILES string

O.O.O.O.O.O.O.O.O.[Na]S[Na]

InChI

1S/2Na.9H2O.S/h;;9*1H2;

InChI key

UIINQVYGFKNSPA-UHFFFAOYSA-N

General description

Sodium sulfide nonahydrate participates in the conversion of nitroxides to amines, via reduction.

Application

Sodium sulfide nonahydrate has been used as a source of H2S, to study the effect of H2S on amyloid fibrils associated with neurodegenerative diseases. It has been used in the preparation of sulfide standards for the quantitative analysis of sulfides in raw wastewater (sewage) samples.
It serves as a catalyst during synthesis of thioamides.
Sodium sulfide nonahydrate has been used as a standard for the quantification of volatile sulfur compounds in cheese samples by gas chromatography. It reacts with 4-(2′-hydroxyaryl)-2-(N,N-dialkylamino)-1,3-dithiolium perchlorates in ethanol at room temperature and boiling ethanol to form 1,3-dithiole-2-thiones and 2′-hydroxyacetophenones, respectively. Sodium sulfide nonahydrate may be used as a reducing agent for the conversion of vic-dibromides to the corresponding olefins via reductive debromination.


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Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B

Storage Class

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

监管及禁止进口产品

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Reaction of 4-(2'-Hydroxyaryl)-1, 3-dithiolium Salts with Sodium Sulfide. A Selective Synthesis of 2'-Hydroxyacetophenones.
Birsa ML.
Synthetic Communications, 33(17), 3071-3076 (2003)
A new reduction system: combination of sodium sulfide (sodium hydrosulfide) with phase transfer agent in a two-phase mixture. Reductive debromination ofvic-dibromides to olefins.
Nakayama J, et al.
Tetrahedron Letters, 24(29), 3001-3004 (1983)
Reduction of nitroxides to amines by sodium sulfide.
Kornblum N and Pinnick HW.
The Journal of Organic Chemistry, 37(12), 2050-2051 (1972)



Global Trade Item Number

SKUGTIN
208043-500G04061837768392
208043-100G04061837768385
208043-5G04061835346578