13468

Sigma-Aldrich

Sodium sulfide hydrate

≥60%, scales

Empirical Formula (Hill Notation):
Na2S · xH2O
CAS Number:
Molecular Weight:
78.04 (anhydrous basis)
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥60%

form

scales

reaction suitability

core: sodium
reagent type: catalyst

anion traces

chloride (Cl-): ≤100 mg/kg

storage temp.

2-8°C

SMILES string

[Na]S[Na]

InChI

1S/2Na.S

InChI key

CXPWOVUZRAFMDA-UHFFFAOYSA-N

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General description

May contain up to 40% water.

Application

Nucleophile and reducing agent derived from H2S; reagent for the synthesis of thiols, thioethers, and acyclic sulfides, di-, and polysulfides; reduces aromatic nitro compounds to amines; reduces sulfoxides to sulfides.

Signal Word

Danger-Danger

hazcat

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

Supp Hazards

EUH031 - EUH071EUH031 - EUH071

storage_class_code

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK Germany

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

Certificate of Analysis

Certificate of Origin

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Total synthesis of xerulinic acid.
Achim Sorg et al.
Angewandte Chemie (International ed. in English), 43(34), 4523-4526 (2004-09-02)
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European journal of medicinal chemistry, 40(1), 15-23 (2005-01-12)
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The Journal of organic chemistry, 70(2), 664-669 (2005-01-18)
Optically pure enantiomers of the chiral tetrahydroxythiepane derivative 3,6-dihydroxy-4,5-O-isopropylidene-thiepane (3) are obtained using a novel protocol in which a library of all possible stereoisomers of 3 is synthesized, followed by two-step stereoselective chromatography, using, first, conventional achiral and, then, chiral...
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