3068-00-6 | 1,2,4-Butanetriol

Packsize	Purity	Availability	Price	Discounted Price
10g	98%	in stock	$13.00	$9.00
25g	98%	in stock	$33.00	$23.00
100g	98%	in stock	$43.00	$30.00

Description

• Catalog Number: AB40817
• Chemical Name: 1,2,4-Butanetriol
• CAS Number: 3068-00-6
• Molecular Formula: C4H10O3
• Molecular Weight: 106.1204
• MDL Number: MFCD00002929
• SMILES: OCCC(CO)O
• NSC Number: 60197

Computed Properties

• Complexity: 37.9
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 3
• Undefined Atom Stereocenter Count: 1
• XLogP3: -1.4

Literature

• Microbial D-xylonate production.

  Applied microbiology and biotechnology 20121001

• Cleavage of pyrene-stabilized RNA bulge loops by trans-(±)-cyclohexane-1,2-diamine.

  Chemistry Central journal 20120101

• Toward a semisynthetic stress response system to engineer microbial solvent tolerance.

  mBio 20120101

• Beneficial effects of pseudoceramide-containing physiologic lipid mixture as a vehicle for topical steroids.

  European journal of dermatology : EJD 20110101

• Impact of nature and length of linker incorporated in agonists on toll-like receptor 9-mediated immune responses.

  Journal of medicinal chemistry 20100513

• Plasma metabolomic profiles reflective of glucose homeostasis in non-diabetic and type 2 diabetic obese African-American women.

  PloS one 20100101

• Production of optically active 1,2,4-butanetriol from corresponding racemate by Microbial stereoinversion.

  Journal of bioscience and bioengineering 20070501

• Thermal stability of beta-lactoglobulin in the presence of aqueous solution of alcohols and polyols.

  International journal of biological macromolecules 20070410

• Measurement of serum total glycerides and free glycerol by high-performance liquid chromatography.

  Journal of lipid research 20060901

• Synthesis and NMDA-receptor affinity of ring and side chain homologous dexoxadrol derivatives.

  Archiv der Pharmazie 20040201

• Microbial synthesis of the energetic material precursor 1,2,4-butanetriol.

  Journal of the American Chemical Society 20031029

• Enantioselective total synthesis of (+)-azimine and (+)-carpaine.

  Organic letters 20031016

• Solubility enhancement of Cox-2 inhibitors using various solvent systems.

  AAPS PharmSciTech 20030901

• Simple synthesis of mite pheromone beta-acaridial and its analogs in the secretion of Caloglyphus polyphyllae (Acari: Acaridae).

  Bioscience, biotechnology, and biochemistry 20030801

• Six-membered cyclic sulfites derived from glucofuranose and 1,2,4-butanetriol.

  Chirality 20010101