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About This Item
Empirical Formula (Hill Notation):
C7H9NO
CAS Number:
Molecular Weight:
123.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Form:
solid
form
solid
Quality Level
mp
123-128 °C
functional group
amine
SMILES string
NCc1ccc(O)cc1
InChI
1S/C7H9NO/c8-5-6-1-3-7(9)4-2-6/h1-4,9H,5,8H2
InChI key
RQJDUEKERVZLLU-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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P R Williamson et al.
The Journal of biological chemistry, 261(20), 9477-9482 (1986-07-15)
The catalysis of amine oxidation by lysyl oxidase has been probed to assess for the likely order of substrate binding and product release and to discriminate between mechanistic alternatives previously proposed for other copper-dependent amine oxidases using molecular oxygen as
C Hartmann et al.
Biochemistry, 32(9), 2234-2241 (1993-03-09)
Anaerobic, rapid-scanning stopped-flow spectroscopy has been used to investigate the UV-visible absorbance changes (300-540 nm) that occur in the spectrum of bovine serum amine oxidase during reduction by benzylamine, p-hydroxybenzylamine, and p-methoxybenzylamine. The reaction of enzyme with benzylamine generates detectable
Qichen Zhan et al.
Small (Weinheim an der Bergstrasse, Germany), 15(3), e1803926-e1803926 (2018-11-30)
Controlled drug release systems can enhance the safety and availability but avoid the side effect of drugs. Herein, the concept of DNA complementary base pairing rules in biology is used to design and prepare a photothermal-triggered drug release system. Adenine
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 776505-25G | 04061832940397 |
| 776505-5G | 04061832940403 |
