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317837

Sigma-Aldrich

Dicyclohexylamine nitrite

97%

Synonym(s):

Dicyclohexylammonium nitrite

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About This Item

Linear Formula:
(C6H11)2NH · HNO2
CAS Number:
3129-91-7
Molecular Weight:
228.33
Beilstein:
3711911
EC Number:
221-515-9
MDL number:
MFCD00013128
UNSPSC Code:
12352100
PubChem Substance ID:
24859102
NACRES:
NA.22

vapor pressure

3.3 mmHg ( 25 °C)

Assay

97%

form

powder

mp

182-183 °C (dec.) (lit.)

storage temp.

2-8°C

SMILES string

ON=O.C1CCC(CC1)NC2CCCCC2

InChI

1S/C12H23N.HNO2/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12;2-1-3/h11-13H,1-10H2;(H,2,3)

InChI key

ZFAKTZXUUNBLEB-UHFFFAOYSA-N

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H228,H302 + H332

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Flam. Sol. 2

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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J L Mitchell et al.
Biochimica et biophysica acta, 840(3), 309-316 (1985-07-05)
Dicyclohexylamine, a spermidine synthase inhibitor, was evaluated for its ability to alter specific polyamine levels in rat hepatoma HTC cells in culture. Media concentrations of 0.5 and 1.0 mM reduced the production of spermidine from putrescine and enhanced the conversion
B G Feuerstein et al.
Cancer research, 45(10), 4950-4954 (1985-10-01)
Growth characteristics, polyamine levels, and distribution of cells in the cell cycle were determined for 9L rat brain tumor cells treated for various periods with 1 mM dicyclohexylamine sulfate (DCHA). Continuous treatment of cells with DCHA caused growth inhibition at
S J Pietr et al.
Mycoses, 32(7), 359-361 (1989-07-01)
Inhibitory doses (ID50) of phenols complexed with dicyclohexylamine are lower (21.4-47.7%) than the inhibitory doses of free phenols. This is demonstrated in vitro by experiments with Aspergillus oryzae and Penicillium expansum on solid medium.
T Wang et al.
Journal of pharmaceutical and biomedical analysis, 15(5), 593-599 (1997-02-01)
A simple, selective, sensitive, accurate and relatively inexpensive method for the determination of palladium in bulk pharmaceutical chemicals (BPC) and their synthetic intermediates by graphite furnace atomic absorption spectroscopy has been developed and validated. Sample preparation by direct dissolution of
R Balint et al.
Virology, 144(1), 194-203 (1985-07-15)
We have reported (R. Balint and S. S. Cohen, 1985, Virology 144, 181-193) that protoplasts from plants infected with turnip yellow mosaic virus (TYMV) continue to produce virus in culture and that newly formed virus particles contained predominantly newly synthesized
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