A8784
N-Acetylputrescine hydrochloride
≥98% (TLC)
Synonym(s):
Monoacetyl-1,4-diaminobutane hydrochloride, N-(4-Aminobutyl)acetamide hydrochloride
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About This Item
Empirical Formula (Hill Notation):
C6H14N2O · HCl
CAS Number:
Molecular Weight:
166.65
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
≥98% (TLC)
Form:
solid
InChI key
XBECFEJUQZXMFE-UHFFFAOYSA-N
SMILES string
Cl.CC(=O)NCCCCN
InChI
1S/C6H14N2O.ClH/c1-6(9)8-5-3-2-4-7;/h2-5,7H2,1H3,(H,8,9);1H
assay
≥98% (TLC)
form
solid
storage temp.
2-8°C
Quality Level
Related Categories
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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W J Hrushesky et al.
Cancer research, 43(8), 3944-3947 (1983-08-01)
Polyamines are small, highly charged, organic cations of possible regulatory importance in RNA-dependent protein synthesis, the production of which reflects cellular growth and division. The cytokinetics of normal cell populations is circadian rhythmic. This is reflected by a circadian rhythmicity
J Lacy et al.
Journal of immunology (Baltimore, Md. : 1950), 135(6), 3772-3776 (1985-12-01)
N,N'-Diacetylputrescine (tetramethylenebisacetamide [TMBA]) and its six carbon analog, hexamethylenebisacetamide (HMBA), inhibited the proliferative response of human B lymphocytes to anti-mu and formalinized Cowan I strain Staphylococcal aureus (SAC) stimulation. In contrast, B cell growth factor-stimulated proliferation of human B cells
S B Rao et al.
Journal of biochemical toxicology, 5(1), 23-32 (1990-01-01)
The mechanism by which chlordecone (CD) amplifies the hepatotoxicity of halomethanes such as CCl4, CHCl3, and BrCCl3 has been a subject of intense study. Recent work has shown that suppression of hepatocellular regeneration leads to accelerated progression of liver injury
M M Abdel-Monem et al.
Journal of chromatography, 222(3), 363-370 (1981-03-13)
A procedure is described for the determination of monoacetylputrescine, N1-acetyl-spermidine and N8-acetylspermidine in human urine. The procedure is based on the high-performance liquid chromatographic separation of the 5-dimethylaminonaphthalene-1-sulfonyl (dansyl) derivatives of these amines using two different chromatographic modes. Monoacetyl-1,6-diaminohexane was
R M Wittich et al.
Molecular and biochemical parasitology, 38(1), 13-17 (1990-01-01)
A novel type of N-acetyltransferase, clearly different from the nuclear and cytosolic polyamine N-acetyltransferases of mammals, was recently found in the intestinal nematode Ascaris suum. The occurrence of this putrescine N-acetylating enzyme has also been noted in the filarial parasite
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