InChI
1S/C7H8O2/c1-5-3-2-4-6(8)7(5)9/h2-4,8-9H,1H3
InChI key
PGSWEKYNAOWQDF-UHFFFAOYSA-N
SMILES string
Cc1cccc(O)c1O
assay
98%
bp
241 °C (lit.)
mp
65-68 °C (lit.)
shipped in
wet ice
storage temp.
2-8°C
Quality Level
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Arved E Reising et al.
Journal of chromatography. A, 1436, 118-132 (2016-02-10)
Lateral transcolumn heterogeneities and the presence of larger voids in a packing (comparable to the particle size) can limit the preparation of efficient chromatographic columns. Optimizing and understanding the packing process provides keys to better packing structures and column performance.
George P Prpich et al.
Biotechnology and bioengineering, 98(5), 1008-1016 (2007-04-28)
The bioproduction of 3-methylcatechol from toluene via Pseudomonas putida MC2 was performed in a solid-liquid two-phase partitioning bioreactor with the intent of increasing yield and productivity over a single-phase system. The solid phase consisted of HYTREL, a thermoplastic polymer that
L E Hüsken et al.
Applied microbiology and biotechnology, 55(5), 571-577 (2001-06-21)
The bioconversion of toluene into 3-methylcatechol was studied as a model system for the production of valuable 3-substituted catechols in general. For this purpose, an improved microbial system for the production of 3-methylcatechol was obtained. Pseudomonas putida strains containing the
Raúl Muñoz et al.
Biodegradation, 19(6), 897-908 (2008-04-15)
The response of Pseudomonas putida F1 to process fluctuations and operational failures during toluene biodegradation was evaluated in a chemostat suspended growth bioreactor. The ability of P. putida F1 to rapidly increase its specific toluene degradation capacity resulted in no
M G Wallis et al.
The Biochemical journal, 266(2), 605-609 (1990-03-01)
A purification procedure has been developed for an extradiol dioxygenase expressed in Escherichia coli, which was originally derived from a Pseudomonas putida strain able to grow on toluidine. Physical and kinetic properties of the enzyme have been investigated. The enzyme
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