Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

19040

Sigma-Aldrich

(±)-1,2,4-Butanetriol

technical, ≥90% (GC)

Synonym(s):

1,2,4-Trihydroxybutane, 1,3,4-Butanetriol, 2-Deoxyerythritol, Butan-1,2,4-triol

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
HOCH2CH2CH(OH)CH2OH
CAS Number:
3068-00-6
Molecular Weight:
106.12
Beilstein:
1733456
EC Number:
221-323-5
MDL number:
MFCD00002929
UNSPSC Code:
12352100
PubChem Substance ID:
57647775
NACRES:
NA.22

grade

technical

Assay

≥90% (GC)

refractive index

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

bp

190-191 °C/18 mmHg (lit.)

density

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

functional group

hydroxyl

SMILES string

OCCC(O)CO

InChI

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

InChI key

ARXKVVRQIIOZGF-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

1,2,4-Butanetriol was used as starting reagent during the synthesis of a series of quaternary ammonium lipids. It was also used in the synthesis of (-)-γ-amino-8-hydroxy butyric acid (GABOB), antiepileptic and hypotensive drug.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

370.4 °F - closed cup

Flash Point(C)

188 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
WXBF4720V
WXBF3542V
WXBF0017V
WXBD7931V
WXBD5679V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

(4S)-(+)-4-(2-Hydroxyethyl)-2,2-dimethyl-1,3-dioxolane 96%

Sigma-Aldrich

571326

(4S)-(+)-4-(2-Hydroxyethyl)-2,2-dimethyl-1,3-dioxolane

L-(S)-Erythrulose: The synthesis of (R)-1, 2, 4-butanetriol and of some related C4 chirons.
Van der EE, et al.
Tetrahedron Letters, 28(40), 4759-4760 (1987)
Ramyar Azizi et al.
Journal of cellular physiology, 234(10), 19039-19047 (2019-03-30)
Recurrent pregnancy loss (RPL) is a one of the most common obstetrical complications. Since, the successful pregnancy occurs in T helper 2 (Th2)-dominant situation and since, Th1 type immunity is related to pregnancy failure, we investigated the effects of cyclosporine
Marcela B Oliveira et al.
Current drug delivery, 15(8), 1112-1122 (2018-05-08)
Bladder cancer is the second type of malignant carcinoma of the urinary tract. The treatment is time-consuming and requires maintenance doses of the drug for long period of time with important side effects. Curcumin has shown evident clinical advances in
Synthesis of cationic lipids from 1, 2, 4-butanetriol.
Ren T and Liu D.
Tetrahedron Letters, 40(2), 209-212 (1999)
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service