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1,4-Diaminobutane dihydrochloride

SIAL/32810 - purum, ≥99.0% (AT)

Synonym: Putrescine dihydrochloride; 1,4-Butanediamine dihydrochloride; 1,4-Diaminobutane dihydrochloride; Tetramethylenediamine dihydrochloride

CAS Number: 333-93-7
Empirical Formula (Hill Notation): C4H12N2 · 2HCl
Molecular Weight: 161.07
EC Number: 206-375-9
MDL Number: MFCD00012526
Linear Formula: NH2(CH2)4NH2 · 2HCl
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-32810-25G 25 g
$113.00
1/EA
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45-32810-100G 100 g
$255.00
1/EA
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assay ≥99.0% (AT)
form powder
grade purum
InChI 1S/C4H12N2.2ClH/c5-3-1-2-4-6;;/h1-6H2;2*1H
InChI key XXWCODXIQWIHQN-UHFFFAOYSA-N
mp 280 °C (dec.) (lit.)
Quality Level 400 
SMILES string Cl[H].Cl[H].NCCCCN
solubility water: soluble 1 g/10 mL, clear, colorless
Application: • Nanocomposite PLA/C20A nanoclay by ultrasound-assisted melt extrusion for adsorption of uremic toxins and methylene blue dye: This study explored the modification of nanoclay with 1,4-diaminobutane dihydrochloride for adsorptive applications, showing enhanced performance in toxin removal (Andrade-Guel et al., 2021 ).
• The Total Synthesis of Spermine Alkaloid Kukoamine Bimesylate: This paper details the synthetic route of spermine alkaloid derivatives using 1,4-diaminobutane dihydrochloride, highlighting methods applicable in medicinal chemistry (Dong, 2018 ).
Biochem/physiol Actions: Binds to the polyamine modulatory site of the NMDA receptor and potentiates NMDA-induced currents; precursor of spermidine.
Biochem/physiol Actions: Binds to the polyamine modulatory site of the NMDA receptor; potentiates NMDA-induced currents.
Purity ≥99.0% (AT)
mp 280 °C (dec.) (lit.)
UNSPSC 12352116

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