Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
NC(CH2)3CN
CAS Number:
Molecular Weight:
94.11
EC Number:
208-861-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1738385
MDL number:
grade
purum
assay
≥98.0% (GC)
refractive index
n20/D 1.434 (lit.), n20/D 1.436
bp
285-287 °C (lit.)
mp
−29 °C (lit.)
density
0.995 g/mL at 25 °C (lit.)
SMILES string
N#CCCCC#N
InChI
1S/C5H6N2/c6-4-2-1-3-5-7/h1-3H2
InChI key
ZTOMUSMDRMJOTH-UHFFFAOYSA-N
Other Notes
Precursor of the corresponding imidate, a cross-linking agent for modifying proteins via amidation according to Davies and Stark
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
233.6 °F - closed cup
flash_point_c
112 °C - closed cup
ppe
Eyeshields, Faceshields, 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.
G E Davies et al.
Proceedings of the National Academy of Sciences of the United States of America, 66(3), 651-656 (1970-07-01)
Amidination of aldolase, glyceraldehyde-3-phosphate dehydrogenase, tryptophan synthetase B protein, L-arabinose isomerase, and the catalytic subunit of E. coli aspartate transcarbamylase with the bifunctional reagent dimethyl suberimidate produces cross-linked proteins, with reaction predominating within oligomers. Disc electrophoresis of a modified protein
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 431850-1G | 04061826663424 |
| 431850-5G | 04061832108469 |
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