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32810

1,4-Diaminobutane dihydrochloride

≥99.0% (AT), powder, purum

Synonym(s):

Putrescine dihydrochloride, 1,4-Butanediamine dihydrochloride, 1,4-Diaminobutane dihydrochloride, Tetramethylenediamine dihydrochloride

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About This Item

Linear Formula:
NH2(CH2)4NH2 · 2HCl
CAS Number:
333-93-7
Molecular Weight:
161.07
NACRES:
NA.22
PubChem Substance ID:
329754336
UNSPSC Code:
12352116
EC Number:
206-375-9
MDL number:
MFCD00012526
Beilstein/REAXYS Number:
3906680
Assay:
≥99.0% (AT)
Form:
powder
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Product Name

1,4-Diaminobutane dihydrochloride, purum, ≥99.0% (AT)

grade

purum

Quality Level

400

assay

≥99.0% (AT)

form

powder

mp

280 °C (dec.) (lit.)

solubility

water: soluble 1 g/10 mL, clear, colorless

SMILES string

Cl[H].Cl[H].NCCCCN

InChI

1S/C4H12N2.2ClH/c5-3-1-2-4-6;;/h1-6H2;2*1H

InChI key

XXWCODXIQWIHQN-UHFFFAOYSA-N

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.
Binds to the polyamine modulatory site of the NMDA receptor; potentiates NMDA-induced currents.

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pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 1

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCP3367
BCCP2668
BCCP1100
BCCP0496
BCCN4543

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Henning Jørgensen et al.
Analytical biochemistry, 317(1), 85-93 (2003-05-06)
Cellulases and hemicellulases are two classes of enzymes produced by filamentous fungi and secreted into the cultivation medium. Both classes of enzymes consist of a subset of classes of which the fungi produce several enzymes with varying molecular mass and
Alkylammonium Hexachlorometallates, IV. Synthesis and Crystal Structure of Bis (1, 4-diammoniobutane) Diaquahydrogen Hexachlororhodate (III) Dichloride,[H3N-(CH2) 4-NH3] 2 [H5O2][RhCl6] Cl2.
Frank W and Rei? GJ.
Chemische Berichte, 129(11), 1355-1359 (1996)
J Kirschbaum et al.
Journal of chromatography. A, 881(1-2), 517-530 (2000-07-25)
The reagent 3,5-dinitrobenzoyl chloride (DNBZ-Cl) was tested for pre-column derivatization of biogenic amines (BAs). Samples were derivatized within 3 min in 1 M NaOH at ambient temperature by adding 2-propanole and 50 mM DNBZ-Cl in acetonitrile. The reaction was terminated
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