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233722

Sigma-Aldrich

Sodium hexanitrocobaltate(III)

ACS reagent

Synonym(s):

Sodium cobaltnitrite, Sodium hexanitritocobaltate(III)

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About This Item

Linear Formula:
Na3Co(NO2)6
CAS Number:
Molecular Weight:
403.94
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NB.24

grade

ACS reagent

form

powder

reaction suitability

reagent type: catalyst
core: cobalt

impurities

≤0.02% insolubles

mp

220 °C (dec.) (lit.)

SMILES string

[Na+].[Na+].[Na+].[O-][N+](=O)[Co-3]([N+]([O-])=O)([N+]([O-])=O)([N+]([O-])=O)([N+]([O-])=O)[N+]([O-])=O

InChI

1S/Co.6NO2.3Na/c;6*2-1-3;;;/q-3;;;;;;;3*+1

InChI key

IMBXIBFCGMYSME-UHFFFAOYSA-N

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Application

Nitrosation reagent for the conversion of aromatic amines to 1,3-diaryltriazenes with excellent yield. Stefane,

signalword

Danger

Hazard Classifications

Carc. 2 - Eye Irrit. 2 - Ox. Sol. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

5.1B - Oxidizing hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

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The thermal dissociation of sodium hexanitrocobaltate (III).
Wendlandt W and Southern T.
Journal of Thermal Analysis and Calorimetry, 2(1), 87-89 (1970)
Bogdan Stefane et al.
The Journal of organic chemistry, 62(21), 7165-7169 (2001-10-24)
Na(3)Co(NO(2))(6) has been investigated as a new reagent for the nitrosation of various substrates containing an amino functionality. Reactions took place in an aqueous solution of the reagent. The pH of the reaction mixture remained in the range 4.3-5. Thus
[Hygienic standard basis for potassium hexanitrocobaltate in the water of reservoirs].
A A Korolev
Gigiena i sanitariia, (10)(10), 72-73 (1980-10-01)
D B Green et al.
Stain technology, 65(1), 15-24 (1990-01-01)
The effect was examined of the chemical decomposition of the potassium stain sodium hexanitrocobaltate (III) (SHC), on its ability to produce stain granules of consistent size that could be used to estimate the K+ contents of stomatal guard cells. Stomata
G Krishnamoorthy et al.
Biochemistry, 41(51), 15277-15287 (2002-12-18)
Information on the structure and dynamics of condensed forms of DNA is important in understanding both natural situations such as DNA packaging and artificial systems such as gene delivery complexes. We have established the fluorescence of bisintercalator 1,1'-(4,4,8,8-tetramethyl-4,8-diazaundecamethylene)bis[4-[[3-methylbenz-1,3-oxazol-2-yl]methylidine]-1,4-dihydroquinolinium] tetraiodide (YOYO-1)

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