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43758

Supelco

(±)-1,2,4-Butanetriol

analytical standard

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About This Item

Linear Formula:
HOCH2CH2CH(OH)CH2OH
CAS Number:
Molecular Weight:
106.12
Beilstein/REAXYS Number:
1733456
EC Number:
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

agency

ASTM® D6584

assay

≥97.0% (GC)

shelf life

limited shelf life, expiry date on the label

refractive index

n20/D 1.473 (lit.)
n20/D 1.474

bp

190-191 °C/18 mmHg (lit.)

density

1.184 g/mL at 20 °C
1.19 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

SMILES string

OCCC(O)CO

InChI

1S/C4H10O3/c5-2-1-4(7)3-6/h4-7H,1-3H2

InChI key

ARXKVVRQIIOZGF-UHFFFAOYSA-N

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General description

1,2,4-Butanetriol (BT) is an important precursor utilized for the synthesis of the energetic material butanetriol trinitrate and several other chemicals. BT is also useful in the manufacture of plasticizers, polymers, cationic lipids, and pharmaceutical compounds.

Application

1,2,4-Butanetriol may be used as an internal standard for the determination of glycerol, and mono-, di-, and triglycerides in vegetable oil methyl esters by capillary gas chromatography and gas chromatography coupled with flame ionization detector (GC-FID).

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Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

ASTM is a registered trademark of American Society for Testing and Materials

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Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

370.4 °F - closed cup

flash_point_c

188 °C - closed cup


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Metabolic engineering of Arabidopsis for butanetriol production using bacterial genes
Abdel G, et al.
Metabolic engineering, 20(1), 109-120 (2013)
Simultaneous determination of glycerol, and mono-, di-and triglycerides in vegetable oil methyl esters by capillary gas chromatography
Plank C and Lorbeer E
Journal of Chromatography A, 697(1-2), 461-468 (1995)
Direct bioconversion of d-xylose to 1, 2, 4-butanetriol in an engineered Escherichia coli
Valdehuesa K, et al.
Process Biochemistry (Oxford, United Kingdom), 49(1), 25-32 (2014)
Validation of a method for determination of free glycerol in biodiesel
Senila L, et al.
Studia Universitatis Babes-Bolyai, Chemia, 345(1-2), 461-468 (2016)
Ming Yan et al.
Journal of molecular biology, 427(8), 1765-1778 (2014-12-21)
The SAGA (Spt-Ada-Gcn5 acetyltransferase) complex performs multiple functions in transcription activation including deubiquitinating histone H2B, which is mediated by a subcomplex called the deubiquitinating module (DUBm). The yeast DUBm comprises a catalytic subunit, Ubp8, and three additional subunits, Sgf11, Sus1

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