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Naftifine Hydrochloride is a synthetic allylamine antifungal agent with broad-spectrum activity against dermatophytes, yeasts, and molds. It exhibits both fungicidal and fungistatic properties and belongs to the allylamine class of antifungals, characterized by a naphthalene ring system connected through an allylamine linker. Applications: Indicated for the treatment of dermatophytosis, cutaneous candidiasis, and tinea versicolor. naftifine hydrochloride is an allylamine antifungal agent with fungicidal and fungistatic properties, particularly effective against dermatophytes. it provides rapid relief of symptoms including itching, burning, and scaling in superficial fungal infections. Category: Active pharmaceutical ingredients. Synonyms: Naftifine HCl. CAS No. 65473-14-5. Product ID: API65473145. Molecular formula: C21H22ClN. Mole weight: 323.9. EINECS: 620-502-9. InChIKey: OLUNPKFOFGZHRT-YGCVIUNWSA-N. Appearance: White to off-white solid.
An antifungal agent. Group: Biochemicals. Alternative Names: Exoderil, Naftin, Suadian. Grades: Highly Purified. CAS No. 65473-14-5. Pack Sizes: 50mg. US Biological Life Sciences.
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Naftifine-N-methyl-d3, Hydrochloride Salt
Labelled Naftifine, which is used as an antifungal agent. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
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Naftopidil
Naftopidil. Group: Biochemicals. Alternative Names: 4- (2-Methoxyphenyl) -a-[ (1-naphthalenyloxy) methyl]-1-piperazineethanol; Naftopil; (+/-)-Naftopidil. Grades: Highly Purified. CAS No. 57149-07-2. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C24H28N2O3. US Biological Life Sciences.
Worldwide
Naftopidil-[d5]
Naftopidil-[d5] is the labelled analogue of Naftopidil, which is a selective α1-adrenergic receptor antagonist or alpha blocker. Synonyms: Naftopidil D5; 4-(2-Methoxyphenyl)-α-[(1-naphthalenyloxy)methyl]-1-piperazineethanol-d5. Grade: >98%. Molecular formula: C24H23D5N2O3. Mole weight: 397.52.
Naftopidil dihydrochloride
Naftopidil DiHCl is a selective 5-HT1A and α1-adrenergic receptor antagonist with IC50 of 0.1 μM and 0.2 μM, respectively. Synonyms: KT-611; KT611; KT 611. Grade: >98%. CAS No. 57149-08-3. Molecular formula: C24H30Cl2N2O3. Mole weight: 465.41.
Naftopidil dihydrochloride
Naftopidil dihydrochloride. Group: Biochemicals. Grades: Highly Purified. CAS No. 57149-08-3. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences.
Worldwide
Naftopidil hydrochloride
Naftopidil hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 1164469-60-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences.
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Nagilactone B
Nagilactone B is isolated from the herbs of Podocarpus neriifolius. Synonyms: (1S)-1,2,3,3a,5aβ,6,10b,10cβ-Octahydro-1,2α,6α-trihydroxy-3aβ,10bα-dimethyl-7-isopropyl-4H,9H-furo[2',3',4':4,5]naphtho[2,1-c]pyran-4,9-dione. Grade: > 95%. CAS No. 19891-51-1. Molecular formula: C19H24O7. Mole weight: 364.4.
Naginata ketone
Naginata ketone. Alternative Names: 1-(3-Methyl-2-furanyl)-3-methyl-2-buten-1-one. CAS No. 6138-88-1. Product ID: FFC-AR-6138881. Molecular formula: C10H12O2. Mole weight: 164.2. IUPAC Name: 3-methyl-1-(3-methylfuran-2-yl)but-2-en-1-one. Alfa Chemistry - ISO 9001:32057 Certified.
NAG-Scaffold
NAG-Scaffold is a dipeptide where the gamma-carboxyl group of one L-glutamic acid molecule forms a peptide bond with the amino group of another L-glutamic acid molecule. The amino group of the first glutamic acid is protected by a benzoxycarbonyl group. This compound is likely used in peptide synthesis or as an intermediate in the preparation of more complex peptide structures. Synonyms: ((S)-4-(((benzyloxy)carbonyl)amino)-4-carboxybutanoyl)-L-glutamic acid; L-Glutamic acid, N-[(phenylmethoxy)carbonyl]-L-γ-glutamyl-; N-[(Phenylmethoxy)carbonyl]-L-γ-glutamyl-L-glutamic acid; N-benzoxycarbonyl-L-gamma-glutamyl-L-glutamic acid; Cbz-gGlu-Glu-OH. Grade: ≥95%. CAS No. 866557-13-3. Molecular formula: C18H22N2O9. Mole weight: 410.38.
N-aheptyl-benzenesulfonamide
N-aheptyl-benzenesulfonamide. CAS No. 66896-46-6. Product ID: ACM66896466. Alfa Chemistry - ISO 9001:32057 Certified.
Nahymenoptaecin-2 precursor
Nahymenoptaecin-2 precursor was found in Nasonia vitripennis [Parasitic wasp] and it has antibacterial activity. Grade: 96% by HPLC.
NAI-802
NAI-802 is a new lantibiotic produced by two different Actinoplanes strains.
Na,im-Bis-Fmoc-D-histidine 99+%
Na,im-Bis-Fmoc-D-histidine 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 2.5g. US Biological Life Sciences.
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Na,im-Bis-Fmoc-L-histidine 99+%
Na,im-Bis-Fmoc-L-histidine 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences.
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NAI-N3
NAI-N3 is a RNA acylation reagent that enables RNA purification. NAI-N3 is a dual-function SHAPE (selective 2-hydroxyl acylation and profiling experiment) probe (RNA structure probe and enrichment)[1]. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. Uses: Scientific research. Category: Signaling pathways. CAS No. 1612756-29-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103006.
Na+/K+-exchanging ATPase
A P-type ATPase that undergoes covalent phosphorylation during the transport cycle. This is a plasma membrane enzyme, ubiquitous in animal cells, that catalyses the efflux of three Na+ and influx of two K+ per ATP hydrolysed. It is involved in generating the plasma membrane electrical potential. Group: Enzymes. Enzyme Commission Number: EC 3.6.3.9. 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-4698; Na+/K+-exchanging ATPase; EC 3.6.3.9. Cat No: EXWM-4698.
Nalbuphine Impurity 11
Nalbuphine Impurity 11. Uses: For analytical and research use. CAS No. 85284-05-5. Molecular formula: C16H20ClNO4. Mole weight: 325.79. Catalog: APB85284055.
Naldemedine tosylate
Naldemedine (S-297995) tosylate is an orally active μ-opioid receptor antagonist (PAMORA)[1]. Naldemedine tosylate shows potent binding affinities (Ki=0.34, 0.43, 0.94 nM, respectively) and antagonist activities (IC50=25.57, 7.09, 16.1 nM, respectively) for recombinant human μ-, δ-, and κ- opioid receptors[2]. Naldemedine can be used in opioid-induced constipation (OIC) research[2]. Naldemedine tosylate is predicted to bind to 3CLpro encoded by SARS-CoV2 genome[3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: S-297995 tosylate. CAS No. 1345728-04-2. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19627A.
Naled-d6
A labeled cholinesterase inhibitor. Insecticide; acaricide. Group: Biochemicals. Alternative Names: Phosphoric Acid 1,2-Dibromo-2,2-dichloroethyl Dimethyl-d6 Ester;1,2-Dibromo-2,2-dichloroethyl Dimethyl-d6 Phosphate; umpet. Grades: Highly Purified. CAS No. 1216605-57-0. Pack Sizes: 10mg. US Biological Life Sciences.
Nalfuranfine Impurity 1/Hydroxycodone EP Impurity C
Nalfuranfine Impurity 1/Hydroxycodone EP Impurity C. Uses: For analytical and research use. Molecular formula: C17H19NO4. Mole weight: 301.34. Catalog: APB08741.
Nalfuranfine Impurity 2
Nalfuranfine Impurity 2. Uses: For analytical and research use. CAS No. 152657-00-6. Molecular formula: C28H34N2O3. Mole weight: 446.59. Catalog: APB152657006.
Nalfuranfine Impurity 4
Nalfuranfine Impurity 4. Uses: For analytical and research use. Molecular formula: C20H25NO4. Mole weight: 343.42. Catalog: APB08742.
Nalfuranfine Impurity 5
Nalfuranfine Impurity 5. Uses: For analytical and research use. Molecular formula: C20H25NO5. Mole weight: 359.42. Catalog: APB08744.
Nalfuranfine Impurity 6
Nalfuranfine Impurity 6. Uses: For analytical and research use. Molecular formula: C28H32N2O5. Mole weight: 476.57. Catalog: APB08743.
Nalfuranfine Impurity 7
Nalfuranfine Impurity 7. Uses: For analytical and research use. CAS No. 163712-68-3. Molecular formula: C28H32N2O5. Mole weight: 476.57. Catalog: APB163712683.
Nalfuranfine Impurity 9
Nalfuranfine Impurity 9. Uses: For analytical and research use. CAS No. 152658-36-1. Molecular formula: C28H32N2O5. Mole weight: 476.57. Catalog: APB152658361.
Nalidixic acid
Nalidixic acid, a quinolone antibiotic, is effective against both gram-positive and gram-negative bacteria. Nalidixic acid acts in a bacteriostatic manner in lower concentrations and is bactericidal in higher concentrations. Nalidixic acid inhibits a subunit of DNA gyrase and topoisomerase IV and reversibly blocks DNA replication in susceptible bacteria[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 389-08-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 g; 10 g; 25 g; 50 g; 100 g. Product ID: HY-B0398.
Nalidixic acid
Nalidixic acid is a synthetic 1,8-naphthyridine antimicrobial agent with a limited bacteriocidal spectrum. It is an inhibitor of bacterial DNA polymerase (DNA gyrase) and avian myeloblastoma virus reverse transcriptase. Synonyms: NSC-82174; NSC82174; 1-Ethyl-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic Acid; 1,4-Dihydro-1-ethyl-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic Acid; Betaxina; Cybis; Dixiben; Eucistin; NegGram; Nelidix; Wintomylon. Grade: >98%. CAS No. 389-08-2. Molecular formula: C12H12N2O3. Mole weight: 232.24.
Nalidixic acid
25g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C12H12N2O3. CAS No. 389-08-2. Prepack ID 37471160-25g. Molecular Weight 232.24. See USA prepack pricing.
Nalidixic Acid, 98+%
Inhibitor of bacterial DNA synthesis. Nalidixic acid is the first of the synthetic quinolone antibiotics. It is a naphthyridone, not a quinolone: its ring structure is a 1,8-naphthyridine nucleus that contains two nitrogen atoms, unlike quinoline, which has a single nitrogen atom.[1] Synthetic quinolone antibiotics were discovered by George Lesher and coworkers as a byproduct of chloroquine manufacture in the 1960s.[1] Used clinically from 1967.[1]. Group: Biochemicals. Alternative Names: 1,4-Dihydro-1-ethyl-7-methyl-1,8-naphthyridin-4-one-3-carboxylic acid; 1-Ethyl-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic acid. Grades: Highly Purified. CAS No. 389-08-2. Pack Sizes: 100g, 250g, 500g, 1Kg. Molecular Formula: C12H12N2O3. US Biological Life Sciences.
Worldwide
Nalidixic Acid 99+%
Inhibitor of bacterial DNA synthesis. Nalidixic acid is the first of the synthetic quinolone antibiotics. It is a naphthyridone, not a quinolone: its ring structure is a 1,8-naphthyridine nucleus that contains two nitrogen atoms, unlike quinoline, which has a single nitrogen atom.[1] Synthetic quinolone antibiotics were discovered by George Lesher and coworkers as a byproduct of chloroquine manufacture in the 1960s.[1] Used clinically from 1967.[1]. Group: Biochemicals. Alternative Names: 1-Ethyl-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylicAcid; 1,4-Dihydro-1-ethyl-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic Acid; Betaxina; Cybis; Dixiben; Eucistin; NegGram; Nelidix; Win 18320; Wintomylon. Grades: Highly Purified. CAS No. 389-08-2. Pack Sizes: 25g, 100g. US Biological Life Sciences.
Worldwide
Nalidixic acid-[d5]
Nalidixic acid-[d5] is the labelled analogue of Nalidixic acid, which is a naphthyridone antibacterial agent similar to quinolones in structure and mechanism. Synonyms: Nalidixic acid-D5; 1-(Ethyl-d5)-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic Acid; 1,4-Dihydro-1-(ethyl-d5)-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic Acid; Betaxina-d5; Cybis-d5; Dixiben-d5; Eucistin-d5; NegGram-d5; Nelidix-d5; Wintomylon-d5; Nalidixic acid-(ethyl-d5). Grade: 95% by HPLC; 98% atom D. CAS No. 1189467-36-4. Molecular formula: C12H7D5N2O3. Mole weight: 237.27.
Nalidixic Acid-d5
Inhibitor of bacterial DNA synthesis. Nalidixic acid is the first of the synthetic quinolone antibiotics. It is a naphthyridone, not a quinolone: its ring structure is a 1,8-naphthyridine nucleus that contains two nitrogen atoms, unlike quinoline, which has a single nitrogen atom.[1] Synthetic quinolone antibiotics were discovered by George Lesher and coworkers as a byproduct of chloroquine manufacture in the 1960s.[1] Used clinically from 1967.[1]. Group: Biochemicals. Alternative Names: 1-(Ethyl-d5)-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic Acid;1,4-Dihydro-1-(ethyl-d5)-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic Acid; Betaxina-d5; Cybis-d5; Dixiben-d5; Eucistin-d5; NegGram-d5; Nelidix-d5; Win 18320-d5; Wintomylon-d5. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Nalidixic acid sodium salt
Nalidixic acid sodium salt. Group: Biochemicals. Alternative Names: 1-Ethyl-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic acid sodium salt. Grades: Highly Purified. CAS No. 3374-5-8. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C12H11N2NaO3. US Biological Life Sciences.
Worldwide
Nalidixic acid sodium salt
25g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C12H11N2NaO3. CAS No. 3374-5-8. Prepack ID 75525039-25g. Molecular Weight 254.22. See USA prepack pricing.
Nalidixic acid sodium salt
Nalidixic acid sodium salt is an inhibitor of bacterial DNA polymerase (DNA gyrase) and avian myeloblastoma virus reverse transcriptase. It inhibits nucleic acid and protein synthesis in Saccharomyces cerevisiae. It is a naphthyridone antibiotic similar in structure and mechanism to quinolones. Synonyms: Baktogram; Sodium nalidixate. Grade: ≥98%. CAS No. 3374-5-8. Molecular formula: C12H11N2NaO3. Mole weight: 254.22.
Isolated from the mold Cladosporium sp. G-10. Acts on N6-(carboxymethyl)lysine, 6-[(carboxymethy)amino]hexanoic acid, sarcosine and N-ethylglycine. It has negligible action on glycine (cf. EC 1.4.3.19 glycine oxidase). Group: Enzymes. Synonyms: N-carboxymethylalkylamine:oxygen oxidoreductase (decarboxymethylating). Enzyme Commission Number: EC 1.5.3.20. 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-1548; N-alkylglycine oxidase; EC 1.5.3.20; N-carboxymethylalkylamine:oxygen oxidoreductase (decarboxymethylating). Cat No: EXWM-1548.
N-Alloc-1,4-butandiamine hydrochloride
N-Alloc-1,4-butandiamine hydrochloride. CAS No. 1049722-10-2. Product ID: ACM1049722102. Mole weight: 208.69. Alfa Chemistry - ISO 9001:32057 Certified.
N-Alloc-L-Tyr-OH DCHA
N-Alloc-L-Tyr-OH DCHA. Synonyms: N Alloc L Tyr OH DCHA. Molecular formula: C25H38N2O5. Mole weight: 446.58.
N-Allyl-4-aminobenzenesulfonamide
N-Allyl-4-aminobenzenesulfonamide. Alternative Names: CHEMBRDG-BB 7992085;AKOS BBS-00000298;AKOS BBB/046;N-ALLYL-4-AMINO-BENZENESULFONAMIDE. CAS No. 117057-51-9. Product ID: ACM117057519. Molecular formula: C9H12N2O2S. Mole weight: 212.27. Alfa Chemistry - ISO 9001:32057 Certified.
N-Allylmaleimide. Group: Biochemicals. Grades: Highly Purified. CAS No. 2973-17-3. Pack Sizes: 25g, 50g, 100g, 250g, 500g. US Biological Life Sciences.
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N-Allyl-N,N-bis(trimethylsilyl)amine
N-Allyl-N,N-bis(trimethylsilyl)amine. Uses: For analytical and research use. CAS No. 7688-51-9. Mole weight: 201.46. EC Number: 231-699-2. Catalog: AP7688519.
A structural analog of Naltrexone with opiate antagonist activity used in pharmaceutical treatment of alcoholism. Other pharmacological applications of this compound aim to reduce food cravings, drug abuse and pulmonary disease in affected individuals. Used as an opioid-induced tranquilizer on large animals in the veterinary industry. Narcotic antagonist. Group: Biochemicals. Alternative Names: (5α). Grades: Highly Purified. CAS No. 55096-26-9. Pack Sizes: 5mg. US Biological Life Sciences.
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Nalmefene
Nalmefene is a BBB-penetrable opioid receptor modulator. Nalmefene is an antagonist of MOR and DOR, and a partial agonist of KOR. Nalmefene has anti-inflammatory and neuroprotective activities. Nalmefene can be used in the research of reducing alcohol-dependent disorders[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 55096-26-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-107744.
Nalmefene hydrochloride impurity p0z3 (dual nalmefene). Uses: For analytical and research use. Molecular formula: C43H51N2O6. Mole weight: 691.89. Catalog: APB11082.
Nalmefene impurity 1
Nalmefene impurity 1. Uses: For analytical and research use. Molecular formula: C18H19NO4. Mole weight: 313.35. Catalog: APB11083.
Nalmefene impurity 10
Nalmefene impurity 10. Uses: For analytical and research use. Molecular formula: C22H25NO3. Mole weight: 351.45. Catalog: APB11088.
Nalmefene impurity 11
Nalmefene impurity 11. Uses: For analytical and research use. CAS No. 144265-45-2. Molecular formula: C22H27NO3. Mole weight: 353.46. Catalog: APB144265452.
Nalmefene impurity 13
Nalmefene impurity 13. Uses: For analytical and research use. Molecular formula: C22H23NO3. Mole weight: 349.43. Catalog: APB11089.
Nalmefene impurity 14
Nalmefene impurity 14. Uses: For analytical and research use. Molecular formula: C43H50N2O6. Mole weight: 690.88. Catalog: APB11090.
Nalmefene impurity 15
Nalmefene impurity 15. Uses: For analytical and research use. Molecular formula: C21H25NO4. Mole weight: 355.43. Catalog: APB11091.
Nalmefene impurity 16
Nalmefene impurity 16. Uses: For analytical and research use. Molecular formula: C21H25NO4. Mole weight: 355.43. Catalog: APB11092.
Nalmefene impurity 17
Nalmefene impurity 17. Uses: For analytical and research use. Molecular formula: C21H25NO4. Mole weight: 355.43. Catalog: APB11093.
Nalmefene impurity 18
Nalmefene impurity 18. Uses: For analytical and research use. Molecular formula: C21H23NO4. Mole weight: 353.42. Catalog: APB11094.
Nalmefene impurity 19
Nalmefene impurity 19. Uses: For analytical and research use. CAS No. 1228646-72-7. Molecular formula: C21H28ClNO4. Mole weight: 393.91. Catalog: APB1228646727.
Nalmefene impurity 2
Nalmefene impurity 2. Uses: For analytical and research use. Molecular formula: C42H50Cl2N2O6. Mole weight: 749.77. Catalog: APB11084.
Nalmefene impurity 5
Nalmefene impurity 5. Uses: For analytical and research use. CAS No. 1058708-33-0. Molecular formula: C21H25NO2. Mole weight: 323.44. Catalog: APB1058708330.
Nalmefene impurity 6
Nalmefene impurity 6. Uses: For analytical and research use. Molecular formula: C25H31NO3. Mole weight: 393.53. Catalog: APB11086.
Nalmefene impurity 7
Nalmefene impurity 7. Uses: For analytical and research use. Molecular formula: C21H25NO4. Mole weight: 355.43. Catalog: APB11085.