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Merck
CN

317837

Sigma-Aldrich

Dicyclohexylamine nitrite

97%

Synonym(s):

Dicyclohexylammonium nitrite

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About This Item

Linear Formula:
(C6H11)2NH · HNO2
CAS Number:
Molecular Weight:
228.33
Beilstein:
3711911
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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vapor pressure

3.3 mmHg ( 25 °C)

Quality Level

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

Signal Word

Warning

Hazard Statements

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

Regulatory Information

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R Witek et al.
Mycoses, 32(7), 362-363 (1989-07-01)
In studies in vitro it has been found that 2,4,5-trichlorophenol in the form of a complex with dicyclohexylamine is two times more active an antifungal agent than free chlorophenol.
L Paulin et al.
Antonie van Leeuwenhoek, 52(6), 483-490 (1986-01-01)
Dicyclohexylamine, which is an inhibitor of bacterial and mammalian spermidine synthase, greatly inhibited the synthesis of spermidine in Pseudomonas aeruginosa. The depletion of spermidine caused by dicyclohexylamine was accompanied by an inhibition of growth of bacteria. This inhibition was reversed
Luigi Cervo et al.
Psychopharmacology, 164(4), 423-428 (2002-11-29)
Hyperforin has been identified as an active constituent of Hypericum perforatum but its importance in the antidepressant effect of this plant's extracts is not really known. To evaluate the antidepressant-like activity of two extracts in relation to the content of
Erol Erçağ et al.
Talanta, 78(3), 772-780 (2009-03-10)
Because of the extremely heterogeneous distribution of explosives in contaminated soils, on-site colorimetric methods are efficient tools to assess the nature and extent of contamination. To meet the need for rapid and low-cost chemical sensing of explosive traces or residues
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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