InChI key
GPSDUZXPYCFOSQ-UHFFFAOYSA-N
InChI
1S/C8H8O2/c1-6-3-2-4-7(5-6)8(9)10/h2-5H,1H3,(H,9,10)
SMILES string
Cc1cccc(c1)C(O)=O
grade
reagent grade
product line
Vetec™
assay
98%
bp
263 °C (lit.)
density
1.054 g/mL at 25 °C (lit.)
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
302.0 °F - closed cup
flash_point_c
150 °C - closed cup
A Cebolla et al.
Applied and environmental microbiology, 62(1), 214-220 (1996-01-01)
A simple procedure to detect the switching on and off of catabolic promoters of Pseudomonas putida, at the level of single cells based on the immunodetection of a reporter epitope expressed on the surface of bacterial cells, has been developed.
K Miura et al.
Biochemistry and molecular biology international, 46(5), 933-941 (1998-12-23)
The transcription of OP2 encoding enzymes for m-toluate catabolism on the Pseudomonas putida TOL plasmid is activated by basal-level XylS protein in the presence of m-toluate or by overproduced XylS protein in the absence of m-toluate. In this study, in
M A Kivisaar et al.
Journal of bacteriology, 171(9), 5111-5116 (1989-09-01)
The utilization of phenol, m-toluate, and salicylate (Phe+, mTol+, and Sal+ characters, respectively) in Pseudomonas sp. strain EST1001 is determined by the coordinated expression of genes placed in different plasmids, i.e., by a multiplasmid system. The natural multiplasmid strain EST1001
L B Jensen et al.
Applied and environmental microbiology, 59(11), 3713-3717 (1993-11-01)
A model substrate-dependent suicide system to biologically contain Pseudomonas putida KT2440 is reported. The system consists of two elements. One element carries a fusion between a synthetic lac promoter (PA1-04/03) and the gef gene, which encodes a killing function. This
Minna M Jussila et al.
Environmental pollution (Barking, Essex : 1987), 139(2), 244-257 (2005-08-02)
A collection of 50 indigenous meta-toluate tolerating bacteria isolated from oil-contaminated rhizosphere of Galega orientalis on selective medium was characterized and identified by classical and molecular methods. 16S rDNA partial sequencing showed the presence of five major lineages of the
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