C108057
N-Cyclohexyl-1,3-propanediamine
99%
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About This Item
Linear Formula:
C6H11NH(CH2)3NH2
CAS Number:
Molecular Weight:
156.27
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
222-001-7
MDL number:
Product Name
N-Cyclohexyl-1,3-propanediamine, 99%
InChI key
ITZPOSYADVYECJ-UHFFFAOYSA-N
InChI
1S/C9H20N2/c10-7-4-8-11-9-5-2-1-3-6-9/h9,11H,1-8,10H2
SMILES string
NCCCNC1CCCCC1
assay
99%
form
liquid
refractive index
n20/D 1.482 (lit.)
bp
120-123 °C/20 mmHg (lit.)
mp
−17-−15 °C (lit.)
density
0.917 g/mL at 25 °C (lit.)
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
213.8 °F - closed cup
flash_point_c
101 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
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M Huber et al.
Cancer research, 55(4), 934-943 (1995-02-15)
Spermine is often the most abundant polyamine in human tumors such as breast carcinomas. However, its specific role in tumor biology is still uncertain, since inhibitors of ornithine decarboxylase such as alpha-difluoromethylornithine depress cell growth while leaving spermine content mostly
P J Chu et al.
European journal of pharmacology, 256(2), 155-160 (1994-04-21)
The facilitating or antagonizing effects of polyamine analogues on N-methyl-DL-aspartate (NMDLA)-induced seizures were investigated using mice. Intracerebroventricular injection of spermidine and spermine, but not putrescine, shortened the latency to appearance of clonic convulsion induced by subcutaneous administration of NMDLA. Injection
Weiping Liu et al.
Chemical & pharmaceutical bulletin, 56(5), 659-662 (2008-05-03)
New JM118 (active form of satraplatin) analogues with N-cyclohexyl-1,3-propanediamine (N-chpda) as the carrier, cis-[Pt(N-chpda)X2] (X2=2Cl(-) (1), oxalate (2), malonate (3), 1,1-cyclobutanedicarboxylate (CBDCA) (3), and 3-hydroxy-1,1-cyclobutanedicarboxylate(HO-CBDCA) (4)), have been synthesized and characterized by elemental analysis and spectroscopic data along with X-ray
Masahiro Ohtani et al.
Cell structure and function, 34(2), 105-113 (2009-10-31)
In order to assess the functional role of the polyamines spermidine and spermine in pancreatic beta-cells, we examined the effect of spermidine and spermine synthase inhibitors, trans-4-methylcyclohexylamine (MCHA) and N-(3-aminopropyl)cyclohexylamine (APCHA), on cellular polyamine and insulin contents, insulin secretion, and
T Beppu et al.
Journal of biochemistry, 117(2), 339-345 (1995-02-01)
The effects of a potent spermidine synthase inhibitor, trans-4-methylcyclohexylamine (4MCHA), and a spermine synthase inhibitor, N-(3-aminopropyl)cyclohexylamine (APCHA), on polyamine biosynthesis and cell growth have been studied in rat hepatoma cells (HTC cells) in culture. Treatment of HTC cells with 4MCHA
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