13325-10-5 | 4-Amino-1-butanol

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$6.00	$4.00
5g	95%	in stock	$7.00	$5.00
10g	95%	in stock	$13.00	$10.00
25g	98%	in stock	$28.00	$19.00
100g	97%	in stock	$97.00	$68.00

Description

• Catalog Number: AA52255
• Chemical Name: 4-Amino-1-butanol
• CAS Number: 13325-10-5
• Molecular Formula: C4H11NO
• Molecular Weight: 89.1362
• MDL Number: MFCD00008230
• SMILES: NCCCCO

Computed Properties

• Complexity: 23.5
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 6
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• XLogP3: -1.1

Literature

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• Physicochemical and biological evaluation of siRNA polyplexes based on PEGylated Poly(amido amine)s.

  Pharmaceutical research 20120201

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  Biomaterials 20120101

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  Journal of controlled release : official journal of the Controlled Release Society 20110310

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  Rapid communications in mass spectrometry : RCM 20080101

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  Acta poloniae pharmaceutica 20080101

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• Evaluation of alkaline phosphatase activity assay for the Reflotron system after substitution of the comparison method.

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• Sequence determination in aliphatic poly(ester amide)s by matrix-assisted laser desorption/ionization time-of-flight and time-of-flight/time-of-flight tandem mass spectrometry.

  Rapid communications in mass spectrometry : RCM 20050101

• Novel fluorescent cationic phospholipid, O-4-napthylimido-1-butyl-DOPC, exhibits unusual foam morphology, forms hexagonal and cubic phases in mixtures, and transfects DNA.

  Chemistry and physics of lipids 20040501

• X-ray and NMR characterization of covalent complexes of trypsin, borate, and alcohols.

  Biochemistry 20040316

• Monolithic scavenger resins by amine functionalizations of poly(4-vinylbenzyl chloride-co-divinylbenzene) PolyHIPE materials.

  Organic letters 20020725

• Formation of a trypsin-borate-4-aminobutanol ternary complex.

  Biochemistry 20020514

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  Alternatives to laboratory animals : ATLA 20020101

• Structure of a human S-adenosylmethionine decarboxylase self-processing ester intermediate and mechanism of putrescine stimulation of processing as revealed by the H243A mutant.

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• Synthesis of new acyclic pyrimidine nucleoside analogs as potential antiviral drugs.

  Journal of medicinal chemistry 19940916