B8153
n-Butylamine-1-14C hydrochloride
aqueous ethanol solution
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About This Item
Linear Formula:
CH3CH2CH214CH2 NH2 ·HCl
CAS Number:
Molecular Weight:
109.60
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
form
aqueous ethanol solution
extent of labeling
1-15 mCi per mmol
storage temp.
2-8°C
SMILES string
Cl.CCC[14CH2]N
Packaging
serum bottle
Physical form
Aqueous solution containing 2% ethanol
Regulatory Information
监管及禁止进口产品
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Michiya Matsusaki et al.
Langmuir : the ACS journal of surfaces and colloids, 22(4), 1396-1399 (2006-02-08)
Surface-grafted peptide nanospheres consisting of hydrophobic poly(L-phenylalanine) with hydrophilic poly(ethylene glycol) (PEG) grafts were successfully prepared by the one-step polymerization of L-phenylalanine N-carboxyanhydride with the dual initiators of hydrophobic n-butylamine and hydrophilic NH2-monoterminated PEG (NH2-PEG). The monodispersed peptide nanospheres were
David W Roberts et al.
Chemical research in toxicology, 20(1), 61-71 (2007-01-18)
Reactions of the strong skin sensitizer hexadec-1-ene-1,3-sultone with sodium hydroxide, sodium methoxide, sodium metabisulfite, sodium butanethiolate, n-butylamine, and aniline have been investigated, and the reaction products have been identified. Most of the nucleophiles studied react by nucleophilic addition (Michael type
Adam J Hopkins et al.
Applied spectroscopy, 67(3), 261-273 (2013-03-05)
Adsorption of small molecular solutes in an aqueous solution to a soft hydrophobic surface is a topic relevant to many fields. In biological and industrial systems, the interfacial environment is often complex, containing an array of salts and organic compounds
Elzbieta Sochacka et al.
Nucleosides, nucleotides & nucleic acids, 27(9), 1045-1060 (2008-08-20)
Reductive amination of 5-formyl-3',5'-di-O-acetyl-2'-deoxyuridine with primary amines and sodium triacetoxyborohydride (NaBH(OAc)(3)) afforded novel enamine derivatives of 5,6-dihydro-2'-deoxyuridine as a result of unexpected 1,4-conjugate reduction of intermediate Schiff bases in addition to the secondary amine derivatives of 2'-deoxyuridine, typical 1,2-reduction products.
Sigrid C Roberts et al.
Antimicrobial agents and chemotherapy, 51(2), 438-445 (2006-11-23)
A number of anticancer and antiparasitic drugs are postulated to target the polyamine biosynthetic pathway and polyamine function, but the exact mode of action of these compounds is still being elucidated. To establish whether polyamine analogs specifically target enzymes of
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