Naphthols
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- Naphthols and their
derivatives are used in the manufacture of dyes; β-naphthol methyl
ether and β-naphthol ethyl ether (neroli oil) are used in cosmetics
manufacture for the preparation of soap perfumes
- Naphthol dyes are true
cold water dyes since many of the components used in naphthol dyeing
are known or suspected carcinogens, they should not be used in your
kitchen.
- 1-Naphthol, or α-naphthol, is a
colorless crystalline solid with the formula c10h7oh.
- It is an isomer of 2-naphthol
differing by the location of the hydroxyl group on naphthalene.
- The naphthols are naphthalene
homologues of phenol, with the hydroxyl group being more reactive
than in the phenols.
- Both isomers are soluble in simple
alcohols, ethers, and chloroform.
- They can be used in the
production of dyes and in organic synthesis.
- Cotton, rayon, and other celluosic
fibers, as well as silk, can also be dyed with azoic or naphthol
dyes.
- Naphthol is sometimes also
spelled as 'napthol' or 'naphtol' the latter is the German spelling.
- They should be used only in a lab, or
in a dye studio in which good laboratory practices are invariably
followed
- Naphthol is an alcohol derived from
naphthalene (C10H8), which is obtained from coal-tar in the form of
white shining crystals of a
strong, disagreeable odor, soluble in alcohol, but insoluble in
water, and employed locally in indolent ulcers and as a disinfectant
in pus-pockets and wounds and skin diseases.
- 1-naphthol has recently been shown to
be selectively toxic to short-term organ cultures of human
colorectal tumor tissue.
- The mechanism underlying 1-naphthol's
selective toxicity is as yet unknown, but may be due to the
formation naphthoquinone
metabolites, which are known to be highly toxic to tumor cells.
- By using high-performance liquid
chromatography with reductive electrochemical detection, it has been
possible to show that 1-naphthol is converted to naphthoquinone
metabolites by rat liver
microsomes.
- At least two metabolic pathways,
independent of cytochrome P-450, appear to be involved.
- Iron-dependent lipid
peroxidation appears to be responsible for at least part of the
conversion of 1-naphthol topredominantly 1,4-naphthoquinone, and it
superoxide anion radical generation by
nadph-cytochrome P-450 reductase could also catalyze this
conversion.
- Workers in tar distillation and
naphthalene distillation are exposed to rather low concentrations of
naphthalene and methylated
naphthalenes and naphthols.
- Naphthols and 1,4-naphthoquinone
identified in the urine appear to be the products of the
hydroxylation of naphthalene present in the breathing-zone air.
- These findings suggest that the
summary concentration of naphthols
in urine can be used as a biomarker for naphthalene exposures
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General
Toxity
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Bayer crop science lp
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Bio catalysis for oxidation of naphthalene
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Mechanisms of toxic injury to isolated
hepatocytes
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Huma health effect
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Preliminary studies on the toxicity and mutageni
city
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Selective toxicity of naphthol to human
colorectal tumour tissue
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Toxicity of carbaryl and 1-naphthol to four species of
freshwater fish
MSDS
- Naphthol-1
- Naphthol spirits 66/3
- 1-Naphthol >98%
- 2-Naphthol, 98%
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1-Amino-2-naphthol-4-sulfonic acid solution
- Alpha-naphthol
- Ultra view universal
alkaline phosphatase red naphthol
- 1-Naphthol (alpha-)
- Naphthol yellow
- Hydroxy naphthol blue
Products
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Three-component synthesis of amidoalkyl naphthols
and carbamato-alkyl
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Daikaffil chemicals india limited
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Naphthols fast salt
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Himanshu dye chem
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Alpha naphthols
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Introduction to naphthols dye
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The synthesis of 1 and 2-naphthols from
napththalene
Patent
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Heterocyclic alkyl naphthols
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Modified naphthalene formaldehyde resin,
tricyclodecane skeleton-containing naphthol
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Process for producing 2-methyl-1-naphthol
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Methylation of α-naphthol to 2-methyl-1-naphthol
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Synthesis of 2-methyl-1-naphthol
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Crystalline nickel chelate of
1-nitroso-2-naphthol and process for producing same
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Process for producing
8-amino-1-naphthol-3,6-disulfonic acid
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Process for the preparation of 1,1'-bi-2-naphthol
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Sulfate and sulfonate beta-naphthol polyglycol
ethers
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Method of preparing naphthol-modified phenolic
resin and epoxy resin
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Process for preparing alpha-naphthol esters of
aliphatic carboxylic acids
Suppliers
- Suppliers of China
- Suppliers of China 1
- Suppliers of China 2
- Suppliers of India
- Suppliers of India 1
- Suppliers of India 2
- Suppliers of India 3
- Suppliers list of Naphthol
Order the CD ROM
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Raw
material
- Extraction and Separation of Benzoic
Acid, 2-Naphthol
- Organic compound
- Phenol
- Phenol and Naphthol Solubility
Manufacturing
- Company from China
- Company another from China
- Company from India
- Company from India1
- Company from India2
- Company from India 3
- Company from India 4
- Manufacture of Naphthol
- Company from Mumbai
- Company from Mumbai 1
- Company from Rajasthan
- List of companies in Naphthol
Market
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Trends and prospects in international trade in
naphthols and their salts
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The 2009 import and export market for
amino-naphthols and other amino-phenols
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Beta naphthol
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Naphthols ironoxide
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Naphthols powder & liquid, ahmedabad cantonment
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Catechols & naphthols
Study
- Catabolism of premercapturic acid
pathway metabolites of naphthalene to naphthols
- Conversion of 1-naphthol to
naphthoquinone metabolites by rat liver microsomes
- Electrochemical sensor for naphthols
based on gold nanoparticles
- An innovative new application for
waste phenolic compounds
- Mechanisms of toxic injury to isolated
hepatocytes by 1-naphthol
- Metabolism of 1-naphthol by tyrosinase
- Simultaneous determination of urinary
1- and 2-naphthols, 3- and 9-phenanthrols
- A study for the proper application of
urinary naphthols
- Urinary naphthols as an indicator of
exposure to naphthalene
Uses
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Acid red 88
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1-amino-2-naphthol-4-sulfonic acid
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an efficient solvent-free protocol for the
synthesis of 1-amidoalkyl-2-naphthols
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Ar-tetrahydro-α-naphthol
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Naphthol or beta naphthol. c10h7oh
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Pan pesticides database - chemicals
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Dyes applications, properties and equipment
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Naphthol green b
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Use of naphthol in pregnancy
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Substrates for western blotting
Process
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Development of commercial grade naphthols
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Highly enantio selective oxidative couplings of
2-naphthols
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Organic chemistry laboratory procedures
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Photogeneration of 1,5-naphthoquinone methides
via excited-state (formal) intra molecular proton
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Sids initial assessment
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Synchronous-derivative phosphorimetric
determination
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