Skip to Content
Merck
All Photos(1)

Documents

E45309

Sigma-Aldrich

Ethyl phenylpropiolate

98%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C6H5C≡CCOOC2H5
CAS Number:
Molecular Weight:
174.20
Beilstein:
639637
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.552 (lit.)

bp

260-270 °C (lit.)

density

1.055 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CCOC(=O)C#Cc1ccccc1

InChI

1S/C11H10O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-7H,2H2,1H3

InChI key

ACJOYTKWHPEIHW-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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

E Patrick et al.
The Journal of investigative dermatology, 88(3 Suppl), 24s-31s (1987-03-01)
The time course, dose response, components of inflammation, and involvement of putative mediators of inflammation in irritation induced by different chemicals was compared using a mouse ear swelling technique. Differences in time courses of inflammation produced by the irritants were
C E Weeks et al.
Proceedings of the National Academy of Sciences of the United States of America, 79(19), 6028-6032 (1982-10-01)
The role of ornithine decarboxylase (OrnDCase, EC 4.1.1.17) and of the polyamines [putrescine (Put), spermidine (Spd), and spermine (Spm)] in mouse skin tumor promotion was investigated by the use of alpha-difluoromethylornithine (CHF2-Orn), an enzyme-activated irreversible inhibitor of OrnDCase. 12-O-Tetradecanoylphorbol 13-acetate
E K Parkinson et al.
Carcinogenesis, 5(5), 687-690 (1984-05-01)
We have studied the effects of the potent tumour promoter phorbol, 12-myristate, 13-acetate (PMA) and two non-promoting hyperplasiogenic compounds ethyl phenylpropriolate (EPP) and the divalent cation ionophore A23187 on the terminal differentiation of normal and transformed human keratinocytes using the
T E Donnelly et al.
Carcinogenesis, 8(12), 1871-1874 (1987-12-01)
We have investigated the effects of various tumor promoting agents on protein kinase C activity in adult female SENCAR mice. Topical application of benzoyl peroxide increased the calcium-independent activity of protein kinase C in the particulate fraction of basal epidermal
J E Paulsen et al.
Cancer research, 43(9), 4126-4131 (1983-09-01)
Quantitative and qualitative changes in epidermal polyamine levels and DNA synthesis (specific activity and labeling index) after a single topical application of 12-O-tetradecanoylphorbol-13-acetate (TPA), mezerein (MEZ), or ethylphenylpropiolate (EPP) in acetone were studied concomitantly in the same epidermal cell population

Articles

MOST offers controlled solar energy harvesting and storage, addressing global energy demands with improved storage techniques.

MOST offers controlled solar energy harvesting and storage, addressing global energy demands with improved storage techniques.

MOST offers controlled solar energy harvesting and storage, addressing global energy demands with improved storage techniques.

MOST offers controlled solar energy harvesting and storage, addressing global energy demands with improved storage techniques.

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