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Naphthalene is an abundant polycyclic aromatic hydrocarbon that is persistent, bioaccumulative, toxic and found in tobacco smoke and urban air. Group: Biochemicals. Grades: Highly Purified. CAS No. 91-20-3. Pack Sizes: 50g, 100g. Molecular Formula: C10H8. US Biological Life Sciences.
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Naphthalene-1
NAPHTHALENE-1,5-DISULFONIC ACID DISODIUM SALT, 95% Assay, powder, Formula: C10H8(SO3Na)2. CAS No. 1655-29-4. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today!
This enzyme is a member of the ring-hydroxylating dioxygenase (RHD) family of bacterial enzymes that play a critical role in the degradation of aromatic compounds, such as polycyclic aromatic hydrocarbons. This enzyme comprises a multicomponent system, containing a reductase that is an iron-sulfur flavoprotein (FAD; EC 1.18.1.3, ferredoxin-NAD+ reductase), an iron-sulfur oxygenase, and ferredoxin. Requires Fe2+. Group: Enzymes. Synonyms: naphthalene dioxygenase; naphthalene oxygenase; NDO. Enzyme Commission Number: EC 1.14.12.12. CAS No. 9074-4-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0681; naphthalene 1,2-dioxygenase; EC 1.14.12.12; 9074-04-8; naphthalene dioxygenase; naphthalene oxygenase; NDO. Cat No: EXWM-0681.
A useful reagent for the derivatization of primary amines, amino acids and small peptides. Group: Biochemicals. Grades: Highly Purified. CAS No. 7149-49-7. Pack Sizes: 100mg. US Biological Life Sciences.
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Naphthalene-2,3-Dicarboxaldehyde
Naphthalene-2,3-Dicarboxaldehyde (2,3-Naphthalenedicarboxaldehyde), a phthaldehyde derivative, is a fungal ASADH inhibitor (K i : 45 ?M). Naphthalene-2,3-Dicarboxaldehyde inhibits the growth of C. albicans CAF2-1 with IC 50 of 58.2 ?M and MIC of 12 ?g/mL [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 2,3-Naphthalenedicarboxaldehyde; Naphthalene-2,3-dialdehyde. CAS No. 7149-49-7. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-W016288.
Naphthalene,2,6-dimethoxy-,radical ion(1+)(9ci)
Heterocyclic Organic Compound. Alternative Names: Naphthalene, 2,6-dimethoxy-, radical ion(1+) (9CI). CAS No. 117119-43-4. Molecular formula: C12H12O2. Catalog: ACM117119434.
Naphthalene-2,6-disulfonic acid
Naphthalene-2,6-disulfonic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 581-75-9. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C10H8O6S2. US Biological Life Sciences.
Naphthalene balls. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2kg, 5kg, 10kg, 25kg, 50kg. US Biological Life Sciences.
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Naphthalene-d8
Heterocyclic Organic Compound. CAS No. 1146-65-2. Molecular formula: C10D8. Mole weight: 136.22. Purity: 99 atom % D. Catalog: ACM1146652.
Naphthalene-d8
Naphthalene-d8, is the labeled analogue of Naphthalene, a polycyclic aromatic hydrocarbons as micropollutants. Group: Biochemicals. Alternative Names: Naphthalene-1,2,3,4,5,6,7,8-d8; Naphthalene (C10D8); Octadeuterionaphthalen e ; Octadeuteronaphthalene ; Perdeuterated Naphthalene; Perdeuterionaphthalene ; Perdeuteronaphthalene. Grades: Highly Purified. CAS No. 1146-65-2. Pack Sizes: 1g, 5g. Molecular Formula: C??D?, Molecular Weight: 136.22. US Biological Life Sciences.
1,1'-Binaphthalene, 2,2'-diiodo-' (BNI) is an organic compound composed of two fused naphthalene rings with two iodine atoms attached to the 2-position of each naphthalene ring. It is an important building block for organic synthesis and has been used in a variety of scientific research applications. This paper will discuss the synthesis method, scientific research application, mechanism of action, biochemical and physiological effects, advantages and limitations for lab experiments, and future directions of BNI. Uses: 1,1'-binaphthalene, 2,2'-diiodo- has been used in a variety of scientific research applications. it has been used in the synthesis of organic compounds, such as 1,2,3-triiodobenzene, 1,2,4-triiodobenzene, and 1,2,3,4-tetraiodobenzene. it has also been used in the synthesis of heterocyclic compounds, such as 1,2,3-triazole and 1,2,3-triazine. additionally, 1,1'-binaphthalene, 2,2'-diiodo- has been used in the synthesis of polymers, such as poly(vinyl chloride) and poly(ethylene terephthalate). Group: Other ligands. CAS No. 76905-80-1. Molecular formula: C20H12I2. Mole weight: 506.1 g/mol. IUPACName: 2-iodo-1-(2-iodonaphthalen-1-yl)naphthalene. Canonical SMILES: C1=CC=C2C (=C1)C=CC (=C2C3=C (C=CC4=CC=CC=C43)I)I. Catalog: ACM76905801.
1-(1-Ethoxyethoxy)-4-fluoronaphthalene is a derivative of 1-Fluoronaphthalene, a fluorinated naphthalene derivative that is metabolized by fungal monooxygenase-epoxide hydrolase. Duloxetine impurity. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 100mg, 1g. Molecular Formula: C14H15FO2, Molecular Weight: 234.27. US Biological Life Sciences.
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1-(1-Methylene-heptyl)-naphthalene
Heterocyclic Organic Compound. Alternative Names: 1-(1-METHYLENE-HEPTYL)-NAPHTHALENE. CAS No. 101720-90-5. Molecular formula: C18H22. Mole weight: 238.36728. Catalog: ACM101720905.
1-(1-Methylene-pentyl)-naphthalene
Heterocyclic Organic Compound. Alternative Names: 1-(1-METHYLENE-PENTYL)-NAPHTHALENE. CAS No. 118319-43-0. Molecular formula: C16H18. Mole weight: 210.31412. Catalog: ACM118319430.
1-(1-p-Tolyl-vinyl)-naphthalene
Heterocyclic Organic Compound. Alternative Names: 1-(1-P-TOLYL-VINYL)-NAPHTHALENE. CAS No. 127236-58-2. Molecular formula: C19H16. Mole weight: 244.33034. Catalog: ACM127236582.
Use as perfume. Group: Non-ionic surfactants. Alternative Names: 2-Naphthalenecarboxaldehyde, 1,2,3,4,5,6,7,8-octahydro-5,5-dimethyl-. CAS No. 68991-96-8. Molecular formula: C13H20O. Mole weight: 192.3. Catalog: ACM68991968.
1,2,3,4-Tetrahydro-1,2,5-naphthalenetriol
1,2,3,4-Tetrahydro-1,2,5-naphthalenetriol is a a reagent used in pharmaceutical synthesis. Group: Biochemicals. Grades: Highly Purified. CAS No. 1478732-43-2. Pack Sizes: 10mg, 25mg. Molecular Formula: C10H12O3, Molecular Weight: 180.2. US Biological Life Sciences.
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1,2,3,4-Tetrahydro-1,2,8-naphthalenetriol
1,2,3,4-Tetrahydro-1,2,8-naphthalenetriol is a reagent is used in the preparation of pharmaceuticals and in organic synthesis. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg, 25mg. Molecular Formula: C10H12O3, Molecular Weight: 180.2. US Biological Life Sciences.
1,2,3,4-Tetrahydro-5-(2-oxiranylmethoxy)-(2R,3S)-rel-2,3-naphthalenediol is used as a reactant in the synthetic preparation of Nadolol (cis-5-{3-[(1,1-dimethylethyl)amino]-2-hydroxypropoxy}-1,2,3,4-tetrahydro-2,3-naphthalenediol) which is a β-adrenergic blocking agent. Group: Biochemicals. Grades: Highly Purified. CAS No. 627081-12-3. Pack Sizes: 500mg, 5g. Molecular Formula: C13H16O4, Molecular Weight: 236.26. US Biological Life Sciences.
1,2,3,4-Tetrahydro-5-(2-oxiranylmethoxy)-(2R,3S)-rel-2,3-naphthalenediol-D5 is an isotopic labelled analog of 1,2,3,4-tetrahydro-5-(2-oxiranylmethoxy)-(2R,3S)-rel-2,3-naphthalenediol. 1,2,3,4-Tetrahydro-5-(2-oxiranylmethoxy)-(2R,3S)-rel-2,3-naphthalenediol is used as a reactant in the synthetic preparation of Nadolol (cis-5-{3-[(1,1-dimethylethyl)amino]-2-hydroxypropoxy}-1,2,3,4-tetrahydro-2,3-naphthalenediol) which is a β-adrenergic blocking agent. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 25mg. Molecular Formula: C13H11D5O4, Molecular Weight: 241.29. US Biological Life Sciences.
Heterocyclic Organic Compound. CAS No. 107110-07-6. Catalog: ACM107110076.
1,2,5,6-Tetrachloronaphthalene
1,2,5,6-Tetrachloronaphthalene is a polychlorinated naphthalene (PCN) with dioxin-like toxic properties. It can induce different biochemical changes by activating cellular aryl hydrocarbon receptor (AhR). Group: Biochemicals. Grades: Highly Purified. CAS No. 67922-22-9. Pack Sizes: 500ug, 2.5mg. Molecular Formula: C10H4Cl4, Molecular Weight: 265.95. US Biological Life Sciences.
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(1,2,5,6-Tetramethyl-d6)naphthalene
(1,2,5,6-Tetramethyl-d6)naphthalene is the labeled analogue of 1,2,5,6-Tetramethylnaphthalene (T303675), a polycyclic aromatic hydrocarbon that has been found in petroleum. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C14H10D6, Molecular Weight: 190.31. US Biological Life Sciences.
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1,2-Diaminonaphthalene
1,2-Diaminonaphthalene. Group: Biochemicals. Alternative Names: 1,2-Naphthalenediamine. Grades: Highly Purified. CAS No. 938-25-0. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C10H10N2. US Biological Life Sciences.
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1,2-Diaminonaphthalene.
Reacts with aldehydes to produce highly fluorescent imidazole derivatives. A fluorometric labeling reagent. It is used for fluorophotometric determination of selenium in some kinds of mushroom. Group: Biochemicals. Alternative Names: 1,2-Naphthalenediamine. Grades: Highly Purified. CAS No. 938-25-0. Pack Sizes: 100mg. US Biological Life Sciences.
1,2-Diamino-naphthalene-5-sulfonamide, Hydrochloride. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 50mg. US Biological Life Sciences.
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1,2-Dihydro-1,1,6-trimethylnaphthalene (>80%)
1,2-Dihydro-1,1,6-trimethyl-naphthalene is responsible for a "kerosene note" or "petrol" aromas in aged Riesling wines. Group: Biochemicals. Grades: Highly Purified. CAS No. 30364-38-6. Pack Sizes: 10mg, 25mg. Molecular Formula: C13H16. US Biological Life Sciences.
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1,2-Dihydroxynaphthalene
1,2-Dihydroxynaphthalene. Group: Ligands for functional metal complexes. Alternative Names: 1,2-Dihydroxynaphthalene; 1,2-DIHYDROXYNAPHTHALENE. CAS No. 574-00-5. Product ID: naphthalene-1,2-diol. Molecular formula: 160.17. Mole weight: C10< / sub>H8< / sub>O2< / sub>. C1=CC=C2C(=C1)C=CC(=C2O)O. NXPPAOGUKPJVDI-UHFFFAOYSA-N. 96%.
1,2-dihydroxynaphthalene dioxygenase
This enzyme is involved in naphthalene degradation. Requires Fe2+. Group: Enzymes. Synonyms: 1,2-DHN dioxygenase; DHNDO; 1,2-dihydroxynaphthalene oxygenase; 1,2-dihydroxynaphthalene:oxygen oxidoreductase. Enzyme Commission Number: EC 1.13.11.56. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0575; 1,2-dihydroxynaphthalene dioxygenase; EC 1.13.11.56; 1,2-DHN dioxygenase; DHNDO; 1,2-dihydroxynaphthalene oxygenase; 1,2-dihydroxynaphthalene:oxygen oxidoreductase. Cat No: EXWM-0575.
1-[[(2E)-3-Phenyl-2-propen-1-yl]oxy]naphthalene
1-[[(2E)-3-Phenyl-2-propen-1-yl]oxy]naphthalene is an impurity of the selective serotonin reuptake inhibitor Dapoxetine (D185700). Group: Biochemicals. Grades: Highly Purified. CAS No. 1091626-77-5. Pack Sizes: 2.5mg. US Biological Life Sciences.
1-(2-Methoxyphenyl)-2-methyl-naphthalene (Mixture) is an intermediate in the synthesis of 1-Methylfluoranthene which is an environmental pollutant that has been found to be a mutagen. Group: Biochemicals. Grades: Highly Purified. CAS No. 910784-96-2. Pack Sizes: 25mg, 50mg. Molecular Formula: C18H16O. US Biological Life Sciences.