232505
1,2-Dihydroxynaphthalene
technical grade
Synonym(s):
1,2-Naphthalenediol
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About This Item
Linear Formula:
C10H6(OH)2
CAS Number:
Molecular Weight:
160.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
grade
technical grade
mp
101-103 °C (lit.)
SMILES string
Oc1ccc2ccccc2c1O
InChI
1S/C10H8O2/c11-9-6-5-7-3-1-2-4-8(7)10(9)12/h1-6,11-12H
InChI key
NXPPAOGUKPJVDI-UHFFFAOYSA-N
General description
1,2-Dihydroxynaphthalene is the most sensitive biomarker for an internal exposure to naphthalene in humans.
Application
1,2-Dihydroxynaphthalene was used as substrate to investigate the rate of oxygen consumption by washed cell suspensions of Corynebacterium sp. strain C125 grown on o-xylene, tetralin or succinate.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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R W Eaton et al.
Journal of bacteriology, 174(23), 7542-7554 (1992-12-01)
The reactions involved in the bacterial metabolism of naphthalene to salicylate have been reinvestigated by using recombinant bacteria carrying genes cloned from plasmid NAH7. When intact cells of Pseudomonas aeruginosa PAO1 carrying DNA fragments encoding the first three enzymes of
Khalid A Ibrahim et al.
Pakistan journal of pharmaceutical sciences, 30(2(Suppl.)), 579-583 (2017-06-27)
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S Sato
Investigative ophthalmology & visual science, 34(11), 3172-3178 (1993-10-01)
Recent studies have indicated that certain aldose reductase inhibitors prevent the formation of cataracts in naphthalene-fed rats. The study was designed to investigate whether aldose reductase itself is involved in the metabolism of naphthalene in the lens and the mechanism
Huilan Fu et al.
Molecular plant pathology, 21(10), 1337-1352 (2020-08-11)
The basal transcription factor II H (TFIIH) is a multicomponent complex. In the present study, we characterized a TFIIH subunit Tfb5 by analysing loss- and gain-of-function mutants to gain a better understanding of the molecular mechanisms underlying stress resistance and
E Andújar et al.
Journal of bacteriology, 182(3), 789-795 (2000-01-14)
A genomic region involved in tetralin biodegradation was recently identified in Sphingomonas strain TFA. We have cloned and sequenced from this region a gene designated thnC, which codes for an extradiol dioxygenase required for tetralin utilization. Comparison to similar sequences
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