A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Na-Fmoc-Nw-(mesitylene-2-sulfonyl)-D-arginine 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g. US Biological Life Sciences.
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Na-Fmoc-Nw-nitro-D-arginine 99+% (HPLC)
Na-Fmoc-Nw-nitro-D-arginine 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g, 25g. US Biological Life Sciences.
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Na-Fmoc-Nw-nitro-L-arginine 99+%
Na-Fmoc-Nw-nitro-L-arginine 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g, 100g. US Biological Life Sciences.
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Na-Fmoc-Nw,Nw'-bis-Boc-D-arginine 99+%
Na-Fmoc-Nw,Nw'-bis-Boc-D-arginine 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences.
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Nafoxidine
Nafoxidine, a nonsteroidal estrogen antagonist, is shown to possess antitumor activity against breast cancer. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Nafoxidene. CAS No. 1845-11-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145716.
Nafoxidine HCl
Nafoxidine HCl is the hydrochloride salt of nafoxidine. Nafoxidine, structurally related to Tamoxifen, is a non-steroidal partial estrogen antagonist. Alternative Names: 1-[2-[4-(6-methoxy-2-phenyl-3,4-dihydronaphthalen-1-yl)phenoxy]ethyl]pyrrolidine;hydrochloride; NAFOXIDINEHYDROCHLORIDE; NafoxidineHCl; 1847-63-8; U11100A. Grades: 95%. CAS No. 1847-63-8. Molecular formula: C29H32CINO2. Mole weight: 462.03.
Nafoxidine Hydrochloride
Nafoxidine is a non-steroidal antiestrogenic drug that is structurally related to Tamoxifen. Nafoxidine is a potent estrogen receptor antagonist that exhibits anti-proliferative properties. Group: Biochemicals. Alternative Names: 1- [2- [4- (3, 4-dihydro-6-methoxy-2-phenyl-1-naphthalenyl) phenoxy] ethyl] pyrrolidine Hydrochloride; 1- [2- [p- (3, 4-dihydro-6-methoxy-2-phenyl-1-naphthyl) phenoxy] ethyl] pyrrolidine Hydrochloride; 11100A; NSC 70735; U 11100; U 11100A; CP-5600. Grades: Highly Purified. CAS No. 1847-63-8. Pack Sizes: 10mg. US Biological Life Sciences.
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Nafronyl
Nafronyl. Group: Biochemicals. Alternative Names: Tetrahydro-a-(1-naphthalenylmethyl)-2-furanpropanoic Acid 2-(Diethylamino)ethyl Ester. Grades: Highly Purified. CAS No. 31329-57-4. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C24H33NO3. US Biological Life Sciences.
Worldwide
Nafronyl oxalate
Naftidrofuryl, being useful in enhancing cellular oxidative, could be used as a vasodilator in the treatment of peripheral and cerebral vascular disorders. Uses: Naftidrofuryl could be used as a vasodilator against peripheral and cerebral vascular disorders. Alternative Names: Nafronyl oxalate; 3200-06-4; 2-(Diethylamino)ethyl 3-(naphthalen-1-yl)-2-((tetrahydrofuran-2-yl)methyl)propanoate oxalate; Naftidrofuryl oxalate; Naftidrofuryl (oxalate); Dubimax. Grades: 98%. CAS No. 3200-6-4. Molecular formula: C26H35NO7. Mole weight: 473.56.
Naftifine hydrochloride
Naftifine is an allylamine antifungal drug for the topical treatment of tinea pedis, tinea cruris, and tinea corporis, probably involves selectively blocking sterol biosynthesis via inhibition of the squalene 2,3-epoxidase enzyme. Alternative Names: AW 105843; AW105843; AW-105843; AW 105-843; SN 105843; SN105843; SN-105843; Naftifine hydrochloride. Grades: >98%. CAS No. 65473-14-5. Molecular formula: C21H21N.HCl. Mole weight: 323.86.
Naftifine Hydrochloride
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.
Worldwide
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.
Worldwide
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 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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NAG 37
NAG 37 is a specialized reagent used in the synthesis of oligonucleotides or other biomolecules, incorporating glycosylated structures. It combines GalNAc (N-acetylgalactosamine), a sugar molecule commonly involved in glycosylation. Phosphoramidite refers to the functional group used to incorporate this glycosylated structure into growing oligonucleotides during solid-phase synthesis, commonly used in creating DNA, RNA, or their analogs with attached glycans. This reagent is valuable for creating modified nucleotides with attached sugars, which are important in studying glycosylation, drug delivery (especially targeting specific cells or tissues like the liver), and other biochemical processes where glycan structures play a critical role. Alternative Names: GalNAc-NAG-37 Phosphoramidite; L-Glutamamide, N2-[[cis-4-[[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]oxy]cyclohexyl]carbonyl]-N-[2-[2-[[3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxy-β-D-galactopyranosyl]oxy]ethoxy]ethyl]-L-α-glutaminyl-N1,N5-bis[2-[2-[[3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxy-β-D-galactopyranosyl]oxy]ethoxy]ethyl]-; N2-[[cis-4-[[[Bis(1-methylethyl)amino](2-cyanoethoxy)phosp. Grades: ≥95%. CAS No. 2199491-27-3. Molecular formula: C80H127N10O37P. Mole weight: 1851.89.
NAG Amine
NAG Amine is a ligand conjugated to biotin, antibodies, or fragments of antibodies to generate a new class of degraders. It has been used in targeted drug delivery, such as oligonucleotide therapy. CAS No. 2199491-25-1. Molecular formula: C64H100N8O34.C2HF3O2. Mole weight: 1639.54.
Nagilactone B
Nagilactone B is isolated from the herbs of Podocarpus neriifolius. Alternative Names: (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. Grades: > 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. Alternative Names: ((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. Grades: ≥95%. CAS No. 866557-13-3. Molecular formula: C18H22N2O9. Mole weight: 410.38.
N-a€heptyl-benzenesulfonamide
N-a€heptyl-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. Grades: 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.
Worldwide
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.
Worldwide
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 tosilate is an agent used for the treatment of opioid-induced constipation (OIC). It was launched in Japan named Symproic by Shionogi. Uses: The treatment of opioid-induced constipation (oic). Alternative Names: Symproic; naldemedine tosilate; Naldemedine (tosylate); Morphinan-7-carboxamide, 17-(cyclopropylmethyl)-6,7-didehydro-4,5-epoxy-3,6,14-trihydroxy-N-(1-methyl-1-(3-phenyl-1,2,4-oxadiazol-5-yl)ethyl)-,(5alpha)-, 4-methylbenzenesulfonate (1:1). CAS No. 1345728-04-2. Molecular formula: C39H42N4O9S. Mole weight: 742.84.
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 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. Alternative Names: 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. Grades: >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
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, 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
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
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. Alternative Names: Baktogram; Sodium nalidixate. Grades: ≥98%. CAS No. 3374-5-8. Molecular formula: C12H11N2NaO3. Mole weight: 254.22.
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.
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. Alternative Names: 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
N-Allylmaleimide, a compound with biomedical research applications, boasts an inhibitory prowess for the growth of select cancer cells. In addition, studies have revealed its potential neuroprotective attributes, making it a promising candidate for neurodegenerative disease treatment. Surmised to exert its effects via hindrance of protein-protein associations, this agent exhibits dynamic impact on applicable systems. Alternative Names: 1-Allyl-1H-pyrrole-2,5-dione. Grades: 98%. CAS No. 2973-17-3. Molecular formula: C7H7NO2. Mole weight: 137.14.
N-Allylmaleimide. Group: Biochemicals. Grades: Highly Purified. CAS No. 2973-17-3. Pack Sizes: 25g, 50g, 100g, 250g, 500g. US Biological Life Sciences.
Worldwide
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.