Organic copper salts
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Copper(II) Dimethyldithiocarbamate 98.0+%, TCI America™
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CAS: 137-29-1 Molecular Formula: C6H12CuN2S4 Molecular Weight (g/mol): 303.962 MDL Number: MFCD00050845 InChI Key: ZOUQIAGHKFLHIA-UHFFFAOYSA-L Synonym: Dimethyldithiocarbamic Acid Copper(II) Salt PubChem CID: 472181 IUPAC Name: copper;N,N-dimethylcarbamodithioate SMILES: CN(C)C(=S)[S-].CN(C)C(=S)[S-].[Cu+2]
| PubChem CID | 472181 |
|---|---|
| CAS | 137-29-1 |
| Molecular Weight (g/mol) | 303.962 |
| MDL Number | MFCD00050845 |
| SMILES | CN(C)C(=S)[S-].CN(C)C(=S)[S-].[Cu+2] |
| Synonym | Dimethyldithiocarbamic Acid Copper(II) Salt |
| IUPAC Name | copper;N,N-dimethylcarbamodithioate |
| InChI Key | ZOUQIAGHKFLHIA-UHFFFAOYSA-L |
| Molecular Formula | C6H12CuN2S4 |
Copper(I) Acetate 93.0+%, TCI America™
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CAS: 598-54-9 Molecular Formula: C2H3CuO2 Molecular Weight (g/mol): 122.59 MDL Number: MFCD00058908 InChI Key: RFKZUAOAYVHBOY-UHFFFAOYSA-M Synonym: copper i acetate,cuprous acetate,copper 1+ acetate,acetic acid, copper 1+ salt,unii-9u3n93lmzb,copper acetate,9u3n93lmzb,acetic acid, copper 1+ salt 1:1,copper 1 acetate PubChem CID: 69023 IUPAC Name: copper(1+);acetate SMILES: CC(=O)[O-].[Cu+]
| PubChem CID | 69023 |
|---|---|
| CAS | 598-54-9 |
| Molecular Weight (g/mol) | 122.59 |
| MDL Number | MFCD00058908 |
| SMILES | CC(=O)[O-].[Cu+] |
| Synonym | copper i acetate,cuprous acetate,copper 1+ acetate,acetic acid, copper 1+ salt,unii-9u3n93lmzb,copper acetate,9u3n93lmzb,acetic acid, copper 1+ salt 1:1,copper 1 acetate |
| IUPAC Name | copper(1+);acetate |
| InChI Key | RFKZUAOAYVHBOY-UHFFFAOYSA-M |
| Molecular Formula | C2H3CuO2 |
Copper(II) Acetate Monohydrate 95.0+%, TCI America™
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CAS: 6046-93-1 Molecular Formula: C4H8CuO5 Molecular Weight (g/mol): 199.65 MDL Number: MFCD00149570 InChI Key: NWFNSTOSIVLCJA-UHFFFAOYSA-L Synonym: copper ii acetate monohydrate,cupric acetate monohydrate,copper diacetate monohydrate,copper acetate monohydrate,copper 2+ acetate, monohydrate,acetic acid, copper 2+ salt, monohydrate,verdigris,copper acetate hydrate,diacetoxycopper hydrate,copper acetate, hydrate PubChem CID: 165397 IUPAC Name: copper(2+) diacetate hydrate SMILES: O.[Cu++].CC([O-])=O.CC([O-])=O
| PubChem CID | 165397 |
|---|---|
| CAS | 6046-93-1 |
| Molecular Weight (g/mol) | 199.65 |
| MDL Number | MFCD00149570 |
| SMILES | O.[Cu++].CC([O-])=O.CC([O-])=O |
| Synonym | copper ii acetate monohydrate,cupric acetate monohydrate,copper diacetate monohydrate,copper acetate monohydrate,copper 2+ acetate, monohydrate,acetic acid, copper 2+ salt, monohydrate,verdigris,copper acetate hydrate,diacetoxycopper hydrate,copper acetate, hydrate |
| IUPAC Name | copper(2+) diacetate hydrate |
| InChI Key | NWFNSTOSIVLCJA-UHFFFAOYSA-L |
| Molecular Formula | C4H8CuO5 |
Copper(II) Bis(2-hydroxyethyl)dithiocarbamate 98.0+%, TCI America™
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CAS: 52611-57-1 Molecular Formula: C10H20CuN2O4S4 Molecular Weight (g/mol): 424.066 MDL Number: MFCD00059149 InChI Key: CWZKOKSQKMDNMW-UHFFFAOYSA-L Synonym: Bis(2-hydroxyethyl)dithiocarbamic Acid Copper(II) Salt PubChem CID: 504564 IUPAC Name: copper;N,N-bis(2-hydroxyethyl)carbamodithioate SMILES: C(CO)N(CCO)C(=S)[S-].C(CO)N(CCO)C(=S)[S-].[Cu+2]
| PubChem CID | 504564 |
|---|---|
| CAS | 52611-57-1 |
| Molecular Weight (g/mol) | 424.066 |
| MDL Number | MFCD00059149 |
| SMILES | C(CO)N(CCO)C(=S)[S-].C(CO)N(CCO)C(=S)[S-].[Cu+2] |
| Synonym | Bis(2-hydroxyethyl)dithiocarbamic Acid Copper(II) Salt |
| IUPAC Name | copper;N,N-bis(2-hydroxyethyl)carbamodithioate |
| InChI Key | CWZKOKSQKMDNMW-UHFFFAOYSA-L |
| Molecular Formula | C10H20CuN2O4S4 |
Monobutyl Phthalate Copper(II) Salt 95.0+%, TCI America™
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CAS: 25215-53-6 Molecular Formula: C24H26CuO8 Molecular Weight (g/mol): 506.01 MDL Number: MFCD00045860 InChI Key: FQHSBEXCSPGVGY-UHFFFAOYSA-L Synonym: Butyl Phthalate Copper(II) Salt, Phthalic Acid Monobutyl Ester Copper(II) Salt PubChem CID: 79467 IUPAC Name: copper;2-butoxycarbonylbenzoate SMILES: CCCCOC(=O)C1=CC=CC=C1C(=O)[O-].CCCCOC(=O)C1=CC=CC=C1C(=O)[O-].[Cu+2]
| PubChem CID | 79467 |
|---|---|
| CAS | 25215-53-6 |
| Molecular Weight (g/mol) | 506.01 |
| MDL Number | MFCD00045860 |
| SMILES | CCCCOC(=O)C1=CC=CC=C1C(=O)[O-].CCCCOC(=O)C1=CC=CC=C1C(=O)[O-].[Cu+2] |
| Synonym | Butyl Phthalate Copper(II) Salt, Phthalic Acid Monobutyl Ester Copper(II) Salt |
| IUPAC Name | copper;2-butoxycarbonylbenzoate |
| InChI Key | FQHSBEXCSPGVGY-UHFFFAOYSA-L |
| Molecular Formula | C24H26CuO8 |
Sigma Aldrich Copper(II) sulfate pentahydrate
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
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| Percent Purity | 99.995% trace metals basis |
|---|---|
| Linear Formula | CuSO4 -+ 5H2O |
| CAS | 7758-99-8 |
| Molecular Weight (g/mol) | 249.69 |
| MDL Number | MFCD00149681 |
| Synonym | Blue Vitriol; Cupric sulfate pentahydrate; Sulfuric acid, copper(II) salt (1:1) pentahydrate |
| RTECS Number | GL8900000 |
| Recommended Storage | Room Temperature |
| Molecular Formula | CuO4S -+ 5H2O |
| EINECS Number | 231-847-6 |
| Melting Point | 110°C |
Apexbio Technology LLC Mafenide Acetate 13009-99-9 200mg
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Mafenide Acetate (CAS 13009-99-9) is a small-molecule inhibitor targeting bacterial nucleotide biosynthesis pathways It is designed to inhibit nucleic acid production by interfering with microbial folic acid synthesis Mafenide Acetate exerts its biological activity primarily through competitive inhibition of para-aminobenzoic acid disrupting folic acid synthesis essential for bacterial growth In in vitro studies Mafenide Acetate demonstrates antibacterial activity against selected Gram-positive and Gram-negative bacteria including Pseudomonas aeruginosa typically showing inhibitory effects with IC50 values in the micromolar range Based on these pharmacological properties Mafenide Acetate holds research potential in microbial infection control and wound care particularly for studies involving burn-associated bacterial infections
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Apexbio Technology LLC Mafenide Acetate 13009-99-9 500mg
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Mafenide Acetate (CAS 13009-99-9) is a small-molecule inhibitor targeting bacterial nucleotide biosynthesis pathways It is designed to inhibit nucleic acid production by interfering with microbial folic acid synthesis Mafenide Acetate exerts its biological activity primarily through competitive inhibition of para-aminobenzoic acid disrupting folic acid synthesis essential for bacterial growth In in vitro studies Mafenide Acetate demonstrates antibacterial activity against selected Gram-positive and Gram-negative bacteria including Pseudomonas aeruginosa typically showing inhibitory effects with IC50 values in the micromolar range Based on these pharmacological properties Mafenide Acetate holds research potential in microbial infection control and wound care particularly for studies involving burn-associated bacterial infections
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Apexbio Technology LLC Roxatidine Acetate HCl 93793-83-0 10mM (in 1mL DMSO)
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Roxatidine Acetate HCl (CAS 93793-83-0) is a selective competitive antagonist of histamine H2 receptors By occupying these receptors it attenuates histamine-induced gastric acid secretion in parietal cells Roxatidine Acetate HCl is primarily utilized in biomedical studies investigating gastric physiology and acid-related gastrointestinal disorders Its receptor-specific inhibitory properties make it valuable in research exploring histaminergic signaling pathways and related pharmacological interventions
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Selleck Chemical LLC Roxatidine Acetate HCl S1880-50mg
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Roxatidine Acetate HCl(HOE 760) is a specific and competitive histamin H2-receptor antagonist with IC50 of 3 2 M inhibits gastric acid secretion and ulcer formation
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Sigma Aldrich Fine Chemicals Biosciences Ammonium acetate puriss. p500G
Ammonium acetate is a colorless hygroscopic solid. It can be prepared by reacting glacial acetic acid with ammonia or ammonium carbonate. It has been reported as potential inhibitor of Pd/C mediated hydrogenolysis of benzyl ether.
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Sigma Aldrich Fine Chemicals Biosciences Amonium acetate puriss. p2.5KG
Ammonium acetate is a colorless hygroscopic solid. It can be prepared by reacting glacial acetic acid with ammonia or ammonium carbonate. It has been reported as potential inhibitor of Pd/C mediated hydrogenolysis of benzyl ether.
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Medchemexpress LLC Magnesium acetate tetrahydrate | 16674-78-5 | MFCD00149214 | 99.5% | 214.45 g/mol | C4H14MgO8 | 50g
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Magnesium acetate tetrahydrate is a carboxylic acid and short-chain fatty acid (SCFAs) Magnesium acetate tetrahydrate activates AMPK increases ROS cleaved caspase 9 PPAR downregulates SREBP-1c ChREBP expression Magnesium acetate tetrahydrate exhibits antifungal activity against Saccharomyces cerevisiae W303-1A Magnesium acetate tetrahydrate regulates energy metabolism Magnesium acetate tetrahydrate has anticancer activity against gastric cancer Magnesium acetate tetrahydrate induces writhing reaction and ulcerative colitis Magnesium acetate tetrahydrate can be used in the researches for gastric cancer ulcerative colitis hepatic steatosis and pain[1][2][3][4][5][6][7][8][9]
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Medchemexpress LLC Magnesium acetate tetrahydrate | 16674-78-5 | MFCD00149214 | 99.5% | 214.45 g/mol | C4H14MgO8 | 100g
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Magnesium acetate tetrahydrate is a carboxylic acid and short-chain fatty acid (SCFAs) Magnesium acetate tetrahydrate activates AMPK increases ROS cleaved caspase 9 PPAR downregulates SREBP-1c ChREBP expression Magnesium acetate tetrahydrate exhibits antifungal activity against Saccharomyces cerevisiae W303-1A Magnesium acetate tetrahydrate regulates energy metabolism Magnesium acetate tetrahydrate has anticancer activity against gastric cancer Magnesium acetate tetrahydrate induces writhing reaction and ulcerative colitis Magnesium acetate tetrahydrate can be used in the researches for gastric cancer ulcerative colitis hepatic steatosis and pain[1][2][3][4][5][6][7][8][9]
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