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32810

Sigma-Aldrich

1,4-Diaminobutane dihydrochloride

purum, ≥99.0% (AT)

Sinonimo/i:

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

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About This Item

Formula condensata:
NH2(CH2)4NH2 · 2HCl
Numero CAS:
333-93-7
Peso molecolare:
161.07
Beilstein:
3906680
Numero CE:
206-375-9
Numero MDL:
MFCD00012526
Codice UNSPSC:
12352116
ID PubChem:
329754336
NACRES:
NA.22

Grado

purum

Livello qualitativo

400

Saggio

≥99.0% (AT)

Forma fisica

powder

Punto di fusione

280 °C (dec.) (lit.)

Solubilità

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

Stringa SMILE

Cl[H].Cl[H].NCCCCN

InChI

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

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Applicazioni

  • 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).

Azioni biochim/fisiol

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

Pittogrammi

Skull and crossbonesCorrosion
GHS06,GHS05

Avvertenze

Danger

Indicazioni di pericolo

H302,H311,H314,H330

Classi di pericolo

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

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 1

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCCH5616
BCCF9152
BCCF9154
BCCF9151
BCCF2125

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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)
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
Valeria M Nurchi et al.
Journal of inorganic biochemistry, 194, 26-33 (2019-02-27)
A comprehensive study of the protonation equilibria of a series of polyamine ligands along with their complex formation equilibria with Cu2+ and Zn2+ is reported in this work. The primary aim of this study has been the achievement of homogeneous
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
Anna Czajkowska-Mysłek et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 105, 82-92 (2017-04-04)
Potential adverse reactions among infants and young children could appear after consumption of food containing small amounts of bioactive amines. This study presents the first assessment of biogenic amines occurrence in ready-to-eat vegetable without/with fish, meat and fruit baby products
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