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P31000

Sigma-Aldrich

Phenylpropargyl aldehyde

96%

Synonym(s):

Phenylpropiolaldehyde, 3-Phenyl-2-propynal

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About This Item

Linear Formula:
C6H5C≡CCHO
CAS Number:
Molecular Weight:
130.14
Beilstein:
1099281
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

96%

refractive index

n20/D 1.604 (lit.)

bp

118 °C/13 mmHg (lit.)

density

1.064 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

[H]C(=O)C#Cc1ccccc1

InChI

1S/C9H6O/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6,8H

InChI key

IDASOVSVRKONFS-UHFFFAOYSA-N

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

201.2 °F - closed cup

Flash Point(C)

94 °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’.

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Customers Also Viewed

M E Grace et al.
The Journal of biological chemistry, 262(35), 16778-16785 (1987-12-15)
beta-Lactamases of all three classes, A, B, and C, are inactivated by phenylpropynal and p-nitrophenylpropynal. The inactivation of RTEM-2 beta-lactamase and of Bacillus cereus beta-lactamase I is accelerated in the presence of A type substrates such as dicloxacillin, quinacillin, and

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