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| Product | Description | |
|---|---|---|
| 1,4-Diaminobutane dihydrochloride | 1,4-Diaminobutane dihydrochloride. Group: Monomers. Alternative Names: Putrescin dihydrochloride. CAS No. 333-93-7. Product ID: Butane-1,4-diamine; dihydrochloride. Molecular formula: 161.07. Mole weight: C4H14Cl2N2. C(CCN)CN.Cl.Cl. InChI=1S/C4H12N2.2ClH/c5-3-1-2-4-6; ; /h1-6H2; 2*1H. XXWCODXIQWIHQN-UHFFFAOYSA-N. 98%. |  |
| 1,4-Diaminobutane dihydrochloride | It is an NMDA receptor agonist produced by the breakdown of amino acids after the death of an organism. It is a polyamine plant growth regulator affecting the synthesis of macromolecules and the development of root systems in plants. Uses: Used in biochemical research. Synonyms: 1,4-Butanediamine Dihydrochloride; Putrescine Dihydrochloride; Putrescine Hydrochloride; Tetramethylenediamine Dihydrochloride. Grades: ≥ 98 %. CAS No. 333-93-7. Molecular formula: C4H12N2.2HCl. Mole weight: 161.07. |  |
| Putrescine dihydrochloride (1,4-Diaminobutane dihydrochloride) | 25g Pack Size. Group: Bioactive Small Molecules, Building Blocks, Research Organics & Inorganics. Formula: NH2(CH2)4NH2 · 2HCl. CAS No. 333-93-7. Prepack ID 25523156-25g. Molecular Weight 161.07. See USA prepack pricing. |  |
| Putrescine Dihydrochloride 99+% | 1,4-Diaminobutane is known to affect the development of plant root systems, its inhibition resulting in a more dominant tap root system. 1,4-Diaminobutane is an amino acid degradation product. Used in the preparation of hexahydropyrimidines as novel hepatitis C virus inhibitors. Also a reagent in the synthesis of antibacterial castor oil-based polyurethane membranes. Group: Biochemicals. Alternative Names: 1,4-Butanediamine Dihydrochloride; 1,4-Diaminobutane Dihydrochloride; Putrescine Dihydrochloride; Putrescine Hydrochloride; Tetramethylenediamine Dihydrochloride. Grades: Highly Purified. CAS No. 333-93-7. Pack Sizes: 25g, 100g, 250g, 500g, 1Kg. Molecular Formula: C?H??Cl?N?. US Biological Life Sciences. |  Worldwide |
| 3,4-Diaminobutanoic acid dihydrochloride | 3,4-Diaminobutanoic acid dihydrochloride, a chemical entity employed in biomedicine, has been found to exhibit promise in the management of select neurological conditions. Furthermore, it has been identified to have potential utility in the therapeutic addressing of several inherited metabolic ailments characterized by augmented homocysteine concentrations in the bloodstream, including but not restricted to, homocystinuria. Moreover, its synthetic applications extend beyond the medical arena and encompass its involvement in the assembly of certain antibiotics and its role as a reagent in chemical synthesis. CAS No. 109754-82-7. Molecular formula: C4H12Cl2N2O2. Mole weight: 191.05. | |
| D-α,γ-Diaminobutyric acid dihydrochloride | Synonyms: H-D-Dab-OH 2HCl; (R)-2,4-Diaminobutanoic acid dihydrochloride. Grades: ≥ 98% (NMR). CAS No. 127531-11-7. Molecular formula: C4H12Cl2N2O2. Mole weight: 191.06. | |
| H-DL-Dab 2HCl | A racemic mixture of selective GABA uptake inhibitors L-DABA and D-DABA. Synonyms: DL-2,4-Diaminobutyric acid dihydrochloride; 2,4-diaminobutanoic acid dihydrochloride. Grades: ≥ 98% (Titration). CAS No. 65427-54-5. Molecular formula: C4H10N2O2·2HCl. Mole weight: 191.05. | |
| L-DABA | L-DABA, (L-2,4-Diaminobutyric acid) is a noncompetitive GABA transaminase inhibitor (IC50 > 500 μM) with antitumor activity in vivo and in vitro. Synonyms: (2S)-2,4-diaminobutanoic acid; 2,4-diaminobutyric acid; 2,4-diaminobutyric acid dihydrochloride, (+-)-isomer; 2,4-diaminobutyric acid dihydrochloride, (S)-isomer; 2,4-diaminobutyric acid monohydrochloride, (+-)-isomer; 2,4-diaminobutyric acid monohydrochloride, (S)-isomer; 2,4-diaminobutyric acid, (+)-isomer; 2,4-diaminobutyric acid, (+-)-isomer; 2,4-diaminobutyric acid, (R)-isomer; 2,4-diaminobutyric acid, (S)-isomer; L-2,4-diaminobutyric acid. CAS No. 1758-80-1. Molecular formula: C4H10N2O2. Mole weight: 118.13. | |
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