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Merck

317837

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24859102
EC Number:
221-515-9
Beilstein/REAXYS Number:
3711911
MDL number:
MFCD00013128

Key Documents

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Product Name

Dicyclohexylamine nitrite, 97%

InChI key

ZFAKTZXUUNBLEB-UHFFFAOYSA-N

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)

SMILES string

ON=O.C1CCC(CC1)NC2CCCCC2

vapor pressure

3.3 mmHg ( 25 °C)

assay

97%

form

powder

mp

182-183 °C (dec.) (lit.)

storage temp.

2-8°C

Quality Level

100

Related Categories

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

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

Storage Class

4.1B - Flammable solid hazardous materials

wgk

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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Certificates of Analysis (COA)

Lot/Batch Number
MKBR3841V
MKBR3836V
MKBR3840V
MKBR3837V
MKBC7229V

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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
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
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
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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