Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
C6H5C≡CCHO
CAS Number:
Molecular Weight:
130.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-942-0
Beilstein/REAXYS Number:
1099281
MDL number:
Assay:
96%
Quality Level
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
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
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| P31000-25G | 04061836690564 |
| P31000-5G | 04061836690571 |
