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| Product | Description | |
|---|---|---|
| L-2-Aminobutanol | L-2-Aminobutanol has potential application as an inhibitor of L-Fucosidases. Group: Biochemicals. Alternative Names: (2S)-2-Amino-1-butanol; (+)-2-Amino-1-butanol; (2S)-2-Aminobutan-1-ol; (S)-2-Aminobutanol; L-(+)-2-Aminobutanol; d-2-Amino-1-butanol. Grades: Highly Purified. CAS No. 5856-62-2. Pack Sizes: 5g. US Biological Life Sciences. |  Worldwide |
| (R) -3-Aminobutanol | (R) -3-Aminobutanol. Uses: For analytical and research use. Group: Impurity standards. CAS No. 61477-40-5. Molecular Formula: C4H11NO. Mole Weight: 89.14. Catalog: APB61477405. |  |
| (S) -3-Aminobutanol | (S) -3-Aminobutanol. Uses: For analytical and research use. Group: Impurity standards. CAS No. 61477-39-2. Molecular Formula: C4H11NO. Mole Weight: 89.14. Catalog: APB61477392. | |
| 4-Amino-1-butanol | 4-Amino-1-butanol is used in the synthesis of NSAIDs with anti-inflammatory properties. Also used in the synthesis of polyamine transport ligands with specificity against human cancers allowing easy access to specific cancer cells. Group: Biochemicals. Alternative Names: 1-Amino-4-butanol; 4-Amino-1-butanol; 4-Aminobutanol; 4-Hydroxy-1-butanamine; 4-Hydroxybutylamine; Butanolamine. Grades: Highly Purified. CAS No. 13325-10-5. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| 4-Amino-1-butanol | A reagent used in the synthesis of NSAIDs and cyclic amines. It is also used in the synthesis of polyamine transport ligands with specificity against human cancers allowing easy access to specific cancer cells. Synonyms: H-Abu(4)-ol; NH2-(CH2)4-OH; δ-Amino-n-butyl alcohol; 4-aminobutan-1-ol; 4-Aminobutanol. Grades: 97 %. CAS No. 13325-10-5. Molecular formula: C4H11NO. Mole weight: 89.14. |  |
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