Skip to Content
Merck
CN
All Photos(2)

Documents

B86206

Sigma-Aldrich

cis-2-Butene-1,4-diol

97%

Synonym(s):

(2Z)-2-Butene-1,4-diol, (Z)-1,4-Dihydroxy-2-butene, (Z)-2-Buten-1,4-diol, (Z)-2-Butene-1,4-diol, cis-1,4-Dihydroxy-2-butene, cis-But-2-en-1,4-diol

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C4H8O2
CAS Number:
Molecular Weight:
88.11
Beilstein:
1679241
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

liquid

refractive index

n20/D 1.478 (lit.)

bp

235 °C (lit.)

mp

4-10 °C (lit.)

density

1.072 g/mL at 20 °C (lit.)

SMILES string

[H]\C(CO)=C(/[H])CO

InChI

1S/C4H8O2/c5-3-1-2-4-6/h1-2,5-6H,3-4H2/b2-1-

InChI key

ORTVZLZNOYNASJ-UPHRSURJSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Pictograms

Health hazardExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - STOT RE 2

Target Organs

Liver,Kidney,Blood

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Yanke Liang et al.
The Journal of organic chemistry, 76(24), 9962-9974 (2011-10-28)
The first psico-oxetanocin analogue of the powerful antiviral natural product, oxetanocin A, has been readily synthesized from cis-2-butene-1,4-diol. Key 2-methyleneoxetane precursors were derived from β-lactones prepared by the carbonylation of epoxides. F(+)-mediated nucleobase incorporation provided the corresponding nucleosides in good
T Okuda et al.
The Journal of antibiotics, 37(7), 718-722 (1984-07-01)
A novel antibiotic, penitricin, Ro 09-0804, has been produced in the culture filtrate of Penicillium aculeatum NR 5165. This antibiotic was purified by repeated extraction of culture filtrate with 1-butanol, and passage of the crude extracts through Sephadex G-10, followed
T Okuda et al.
The Journal of antibiotics, 37(7), 723-727 (1984-07-01)
A novel antibiotic, penitricin showing anti-Gram-negative activity, has been isolated from the culture filtrate of Penicillium aculeatum. Chemical and physico-chemical studies determined the structure of penitricin as hydroxymethylcyclopropenone (1), which was confirmed by chemical synthesis from propargyl alcohol. Biological activity
Dong-Myeong Shin et al.
Advanced materials (Deerfield Beach, Fla.), 32(10), e1905771-e1905771 (2020-01-28)
Lithium-ion batteries have remained a state-of-the-art electrochemical energy storage technology for decades now, but their energy densities are limited by electrode materials and conventional liquid electrolytes can pose significant safety concerns. Lithium metal batteries featuring Li metal anodes, solid polymer
Chun-xiu Pan et al.
Journal of Zhejiang University. Science. B, 6(1), 74-78 (2004-12-14)
The cis and trans isomers separation of 2-butene-1,4-diol and lafutidine were studied by HPLC on two kinds of chiral columns: (S,S)-Whelk-O 1 and ChiraSpher. The isomers of 2-butene-1,4-diol can be separated on both chiral columns while the isomers of lafutidine

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