317837
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
Recommended Products
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
Signal Word
Warning
Hazard Statements
Precautionary 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
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A F Tiburcio et al.
Plant cell, tissue and organ culture, 9, 111-120 (1987-01-01)
We studied the effects of inhibitors of ornithine decarboxylase (ODC), arginine decarboxylase (ADC) and spermidine synthase (Spd synthase) on organogenesis and the titers of polyamines (PA) and alkaloids in tobacco calli. DL-alpha-diffluromethylarginine (DFMA) and D-arginine (D-Arg), both inhibitors of ADC
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
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
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
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
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