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-O-di-tert-butyl-malonyl-L-tyrosine ≥95% (TLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 168135-77-1. Pack Sizes: 100mg, 250mg, 25mg, 1g. US Biological Life Sciences.
Worldwide
Nafoxidine
Nafoxidine, a nonsteroidal estrogen antagonist, is shown to possess antitumor activity against breast cancer. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Nafoxidene. CAS No. 1845-11-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145716.
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.
Naftazone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: naftazone;2-[1-Oxonaphthalen-2(1H)-ylidene]hydrazinecarboxamide;Karbinone;Mediaven. Product Category: Heterocyclic Organic Compound. CAS No. 15687-37-3. Molecular formula: C11H9N3O2. Mole weight: 0. Product ID: ACM15687373. Alfa Chemistry ISO 9001:2015 Certified.
Naftazone
Naftazone is a naphthoquinone derivative, it can be used for the research of venous insufciency. Naftazone protects blood vessels, increases venous tonicity and capillary resistance, and improves lymphatic and venous circulation [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 15687-37-3. Pack Sizes: 5 mg; 10 mg. Product ID: HY-108011.
Naftidrofuryl oxalate
Naftidrofuryl oxalate (Nafronyl oxalate salt) is a drug used in the management of peripheral and cerebral vascular disorders as a vasodilator, enhance cellular oxidative capacity, and may also be a 5-HT2 receptor antagonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Nafronyl oxalate salt. CAS No. 3200-6-4. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1107.
Naftifine-[d3] Hydrochloride
Naftifine-[d3] Hydrochloride is the labelled salt of Naftifine. Naftifine is a topical, synthetic, broad spectrum allylamine derivate. It has antifungal, antibacterial and anti-inflammatory activity and is used for the treatment of tinea pedis, tinea cruris, and tinea corporis. Synonyms: Naftifine D3 HCl; (E)-N-(Methyl-d3)-N-(3-phenyl-2-propen-1-yl)-1-naphthalenemethanamine Hydrochloride; (E)-N-Cinnamyl-N-(methyl-d3)-1-naphthalenemethanamine Hydrochloride; Exoderil-d3; Naftifungin-d3; Naftin-d3. Grade: 98%; ≥99% atom D. CAS No. 1246833-81-7. Molecular formula: C21H18D3N.HCl. Mole weight: 326.86.
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. Synonyms: AW 105843; AW105843; AW-105843; AW 105-843; SN 105843; SN105843; SN-105843; Naftifine hydrochloride. Grade: >98%. CAS No. 65473-14-5. Molecular formula: C21H21N.HCl. Mole weight: 323.86.
Naftifine hydrochloride
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Naftifine hydrochloride
Naftifine hydrochloride is an antibiotic. Naftifine hydrochloride has antifungal activity against dermatophytes, aspergilli, Sporothrix schenckii , and yeasts of the genus Candida. Naftifine hydrochloride can be used for the research of superficial dermatomycoses inhibition [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 65473-14-5. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-B0518A.
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 (KT-611) is is a selective alpha1-adrenoceptor antagonist, with K i s of 3.7 nM, 20 nM and 1.2 nM for the cloned human α 1a -, α 1b - and α 1d -adrenoceptor subtypes, respectively. Naftopidil has antiproliferative effects. Naftopidil can be used for the research of prostate hyperplasia [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: KT-611; BM-15275. CAS No. 57149-07-2. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g; 10 g. Product ID: HY-B0391.
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.
A a-1-Adrenergic receptor antagonist, antihypertensive. Group: Biochemicals. Alternative Names: 4- (2-Methoxyphenyl) -a-[ (1-naphthalenyloxy) methyl]-1-piperazineethanol. Grades: Highly Purified. Pack Sizes: 50mg. 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 dihydrochloride. Group: Biochemicals. Grades: Highly Purified. CAS No. 57149-08-3. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences.
Worldwide
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.
Na,g-Bis-Fmoc-D-2,4-diaminobutyric acid 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 1217645-10-7. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences.
Worldwide
Na,g-Bis-Fmoc-L-2,4-diaminobutyric acid 99+%
Na,g-Bis-Fmoc-L-2,4-diaminobutyric acid 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g, 25g. US Biological Life Sciences.
Worldwide
Na,g-Bis-Z-L-2,4-diaminobutyric acid 99+%
Na,g-Bis-Z-L-2,4-diaminobutyric acid 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences.
Worldwide
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.
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.
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.
NAI-DMAC
NAI-DMAC. Uses: Designed for use in research and industrial production. Additional or Alternative Names: N-(4-Tert-butylphenyl)-1,8-naphthalimide-9,9-dimethyl-9,10-dihydroacridine. Product Category: Organic Light Emitting Diode (OLED). CAS No. 2196247-08-0. Molecular formula: C37H32N2O2. Mole weight: 536.66 g/mol. Product ID: ACM2196247080. Alfa Chemistry ISO 9001:2015 Certified. Categories: Naida McCullough.
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. Group: Signaling pathways. CAS No. 1612756-29-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103006.
NAI-N3
NAI-N3 is a probe for icSHAPE (in vivo click selective 2'-hydroxyl acylation and profiling experiment). It acylates the 2'-OH in ssRNA and enables RNA structure profiling in vivo and ex vivo for all four bases. NAI-N3 can be used for site-specific RNA acylation using the RAIL (RNA Acylation at Induced Loops) method or in Apta-Seq to discover new aptamers in selected pools. Uses: Designed for use in research and industrial production. Additional or Alternative Names: NAI-N3; NAIN3; NAI N3. Product Category: Others. Appearance: Solid powder. CAS No. 1612756-29-2. Molecular formula: C10H8N6O. Mole weight: 228.22. Purity: >98%. IUPACName: (2-(azidomethyl)pyridin-3-yl)(1H-imidazol-1-yl)methanone. Canonical SMILES: [N-]=[N+]=NCC1=C(C=CC=N1)C(N2C=CN=C2)=O. Product ID: ACM1612756292. Alfa Chemistry ISO 9001:2015 Certified. Categories: Nai Nabhannu La 5.
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-D3 solution
100 ?g/mL in methanol, ampule of 1 mL, certified reference material. Group: Opiates / synthetic analgesic drug standards.
Naldemedine tosylate
Naldemedine (S-297995) tosylate is an orally active μ-opioid receptor antagonist (PAMORA) [1]. Naldemedine tosylate shows potent binding affinities ( K i =0.34, 0.43, 0.94 nM, respectively) and antagonist activities ( IC 50 =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 3CL pro encoded by SARS-CoV2 genome [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: S-297995 tosylate. CAS No. 1345728-04-2. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-19627A.
Naled
A cholinesterase inhibitor. Insecticide; acaricide. Group: Biochemicals. Alternative Names: Phosphoric Acid 1,2-Dibromo-2,2-dichloroethyl Dimethyl Ester;1,2-Dibromo-2,2-dichloroethyl Dimethyl Phosphate; Bromchlophos; Bromex;Dibrom; ENT 24988; Trumpet. Grades: Highly Purified. CAS No. 300-76-5. Pack Sizes: 1g. Molecular Formula: C?H?Br?Cl?O?P, Molecular Weight: 380.78. US Biological Life Sciences.
Worldwide
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.
Worldwide
Nalfurafine (TRK-820)
Nalfurafine is a κ-opioid receptor (KOR) agonist (EC50 = 0.05nM for human receptors expressed in CHO cell membranes).1 It is selective for κ-opioid over μ- and δ-opioid receptors (EC50s = 0.72 and 74.1nM, respectively). Nalfurafine (≥30ug/kg) reduces scratching behavior induced by chloroquine in mice, as well as locomotor activity when administered at a dose of 100ug/kg.2 In rats, nalfurafine (≥0.01mg/kg) reduces intracranial self-stimulation, lactic acid-induced stretching behavior, and scratching behavior induced by intradermal administration of serotonin.3 Nalfurafine is also an orexin 1 receptor (OX1R) antagonist (Ki = 250nM).4. Group: Biochemicals. Alternative Names: (2E)-N-[(5α,6 β)-17-(cyclopropylmethyl)-4,5-epoxy-3,14-dihydroxymorphinan-6-yl]-3-(3-furanyl)-N-methyl-2-propenamide; TRK-820. Grades: Highly Purified. CAS No. 152657-84-6. Pack Sizes: 1mg, 5mg, 10mg. Molecular Formula: C28H32N2O5, Molecular Weight: 476.56. US Biological Life Sciences.
Worldwide
Nalfuranfine Impurity 2
Nalfuranfine Impurity 2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 152657-00-6. Molecular formula: C28H34N2O3. Mole weight: 446.59. Catalog: APB152657006.
Nalfuranfine Impurity 9
Nalfuranfine Impurity 9. Uses: For analytical and research use. Group: Impurity standards. CAS No. 152658-36-1. Molecular formula: C28H32N2O5. Mole weight: 476.57. Catalog: APB152658361.
Nalidixic acid
analytical standard. Group: Application areas.
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 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, 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. Group: Natural products. CAS No. 389-08-2. Pack Sizes: 10 mM * 1 mL; 5 g; 10 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]
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-(ethyl-d5)
analytical standard. Group: Drugs & metabolites.
Nalidixic acid sodium salt
Nalidixic acid sodium salt, 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] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 3374-5-8. Pack Sizes: 50 mg; 100 mg. Product ID: HY-B0398A.
Nalidixic acid sodium salt
Nalidixic acid sodium salt, 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. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. CAS No. 3374-5-8. Molecular formula: C12H11N2NaO3. Mole weight: 254.22. Product ID: ACM3374058. Alfa Chemistry ISO 9001:2015 Certified.