317837
Dicyclohexylamine nitrite
97%
Synonym(s):
Dicyclohexylammonium nitrite
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All Photos(2)
About This Item
Linear Formula:
(C6H11)2NH · HNO2
CAS Number:
Molecular Weight:
228.33
Beilstein/REAXYS Number:
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
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Flam. Sol. 2
Storage Class
4.1B - Flammable solid hazardous materials
wgk_germany
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, 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
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
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
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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