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| Product | Description | |
|---|---|---|
| Cadmium Zinc Sulfide Yellow Nanopowder | Cadmium Zinc Sulfide Yellow Nanopowder. Group: Nanopowder compounds. CAS No. 8048-7-5. Molecular formula: 209.75g/mol. Mole weight: CdSZn. 99.9 %. |  |
| Cadmium Zinc Telluride (CZT) Sputtering Targets | Cadmium Zinc Telluride (CZT) Sputtering Targets. Group: Sputtering targets. Alternative Names: Cadmium Zinc Telluride (CZT) Sputtering Targets, CdZnTe Sputtering Target, CZT Sputtering Target, CZT Sputter Target, CZT Target, Cadmium Zinc Telluride Sputtering Target, Cadmium Zinc Telluride Sputter Target, Cadmium Zinc Telluride Target. 99.9%. | |
| Cadmuim Sulphide/Zinc Sulphide-PEG-NH? Quantum Dots | Cadmuim Sulphide/Zinc Sulphide-PEG-NH2 Quantum Dots. Group: Cds/zns quantum dots. 99.9%. | |
| Cadonilimab | Cadonilimab (AK104) is a humanized tetravalent IgG1 bispecific antibody targeting PD1/CTLA4. Cadonilimab blocks both PD-1 and CTLA-4 pathways, thereby relieving their corresponding immunosuppressive effects and reversing tumor specific T cell exhaustion. Cadonilimab significantly downregulates Fc-mediated effector functions, including antibody-dependent cell-mediated cytotoxicity (ADCC), antibody-dependent cellular phagocytosis (ADCP), complement dependent cytotoxicity (CDC). Cadonilimab can be used for research of metastatic cervical cancer, as well as other malignancies such as gastric cancer, GEJ adenocarcinoma and non-small cell lung cancer (NSCLC) [1] [2] [3] [4]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: AK104. CAS No. 2394841-59-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99117. |  |
| cADP-Ribose (cADPR) Ammonium Salt | Cyclic ADP-ribose ammonium is a potent calcium-mobilized second messenger synthesized from NAD+ by ADP-ribosyl cyclase. It increases cytosolic calcium mainly by Ryanodine receptor-mediated release from endoplasmic reticulum and extracellular influx through the opening of TRPM2 channels. Synonyms: cADP-Ribose Ammonium Salt; cADPR Ammonium Salt; cyclic ADP-ribose ammonium salt; Cyclic Adenosine Diphosphate Ribose ammonium salt; Cyclic adenosine 5'-diphosphate ribose ammonium salt. Grades: 90%. Molecular formula: C15H21N5O13P2.x(NH3). Mole weight: 541.30 (free base). |  |
| Cadralazine | Cadralazine (ISF 2469) is an orally active antihypertensive agent. Cadralazine is a peripheral arteriolar vasodilator [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ISF 2469. CAS No. 64241-34-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-106538. | |
| Cadrofloxacin | Cadrofloxacin, also known as Caderofloxacin and CS-940, is a novel fluoroquinolone antibacterial. The activities of CS-940 against gram-positive cocci and gram-negative rods, including methicillin-susceptible Staphylococcus aureus and penicillin-resistant Streptococcus pneumoniae, were comparable to those of tosufloxacin, with MICs at which 90% of the strains were inhibited (MIC90s) of 0.5 microg/ml or less. Against methicillin-resistant S. aureus, CS-940 was as active as tosufloxacin, with a MIC90 of 16 microg/ml. The efficacy of CS-940 against murine respiratory infections due to S. pneumoniae or Haemophilus influenzae was better than those of tosufloxacin and sparfloxacin. The efficacy of oral doses of CS-940 reflected not only potent in vitro activity but also a high transmigration ratio from the bloodstream to lung tissues. Uses: Designed for use in research and industrial production. Additional or Alternative Names: CS-940; CS 940; CS940; Cadrofloxacin; Caderofloxacin; Cadrofloxacin hydrochloride; Cadrofloxacin HCl. Product Category: Others. Appearance: Solid powder. CAS No. 153808-85-6. Molecular formula: C19H20F3N3O4. Mole weight: 411.38. Purity: >98%. IUPACName: (S)-1-cyclopropyl-8-(difluoromethoxy)-6-fluoro-7-(3-methylpiperazin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid. Canonical SMILES: O=C(C1=CN(C2CC2)C3=C(C=C(F)C(N4C[C@H](C)NCC4)=C3OC(F)F)C1=O)O. Density: 1.458g/cm³. Product ID: ACM153808856. Alfa Chem |  |
| Cadrofloxacin | Cadrofloxacin (Caderofloxacin; CS-940), a orally active fluoroquinolone, is effective against aerobic/anaerobic Gram-positive and Gram-negative bacteria. Cadrofloxacin can be used for the research of infectious diseases [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Caderofloxacin; CS-940. CAS No. 153808-85-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-116228. | |
| Cadusafos | analytical standard. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. Alternative Names: Cadusafos. |  |
| Cadusafos | Cadusafos. Group: Biochemicals. Alternative Names: Phosphorodithioic acid O-ethyl S,S-bis(1-methylpropyl) ester. Grades: Highly Purified. CAS No. 95465-99-9. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C10H23O2PS2. US Biological Life Sciences. |  Worldwide |
| CADY | CADY is a secondary amphiphilic peptide that has been shown to efficiently deliver short nucleic acids, especially siRNA, but cannot deliver any peptides, even short negatively charged peptides. Synonyms: Ac-Gly-Leu-Trp-Arg-Ala-Leu-Trp-Arg-Leu-Leu-Arg-Ser-Leu-Trp-Arg-Leu-Leu-Trp-Arg-Ala-cysteamide. Grades: >98%. Molecular formula: C132H205N41O26S. Mole weight: 2814.41. | |
| Caenacin-1 | Caenacin-1 was found in Caenorhabditis elegans. It has antifungal activity. | |
| Caenacin-5 | Caenacin-5 was found in Caenorhabditis elegans. It has antifungal activity. | |
| Caerin 11 | Caerin 11 was found in Litoria peronii. It has antibacterial activity. | |
| Caerin-1.1 | Caerin-1.1 was found in Litoria gilleni. Caerin-1.1 is an antibacterial and antiviral peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-1.10 | Caerin-1.10 was found in Litoria rothii. Caerin-1.10 is an antibacterial peptide with wide spectrum of activity. | |
| Caerin 1.11 | Caerin 1.11 was produced by Litoria eucnemis. Caerin 1.11 is a cationic amphipathic alpha-helical antimicrobial peptide with weak or no activity against both Gram-positive and Gram-negative bacteria. It is weakly active against E.coli (MIC=25 μM), E.cloacae (MIC=50 μM), K.pneumoniae (MIC=25 μM), and S.haemolyticus (MIC=50 μM). | |
| Caerin 1.12 | Caerin 1.12 is originally isolated from Litoria caerulea. It has antibacterial activity. | |
| Caerin-1.1.2 | Caerin-1.1.2 has antibacterial activity. The source of Caerin-1.1.2 is Litoria caerulea. Grades: >97% by HPLC. Molecular formula: C107H178N30O26. Mole weight: 2300.74. | |
| Caerin 1.13 | Caerin 1.13 is originally isolated from Litoria caerulea. It has antibacterial activity. | |
| Caerin 1.14 | Caerin 1.14 is originally isolated from Litoria caerulea. It has antibacterial activity. | |
| Caerin 1.15 | Caerin 1.15 is originally isolated from Litoria caerulea. It has antibacterial activity. | |
| Caerin-1.17 | Caerin-1.17 was found in Litoria gracilenta. Caerin-1.17 shows significant activity against Gram-positive organisms, but is less effective against Gram-negative organisms. Grades: >95% by HPLC. Molecular formula: C124H206N32O29. Mole weight: 2609.15. | |
| Caerin-1.18 | Caerin-1.18 was found in Litoria gracilenta. It shows significant activity against Gram-positive organisms, but is less effective against Gram-negative organisms. Grades: >96% by HPLC. | |
| Caerin-1.19 | Caerin-1.19 was found in Litoria gracilenta. Caerin-1.19 shows significant activity against Gram-positive organisms, but is less effective against Gram-negative organisms. | |
| Caerin-1.2 | Caerin 1.2 was found in Litoria caerula. Caerin 1.2 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin 1.20 | Caerin 1.20 has antibacterial activity. The source of Caerin 1.20 is the skin secretions, hybrid between female Litoria splendida and male Litoria caerulea, Australia. Grades: >98% by HPLC. Molecular formula: C124H201N33O28. Mole weight: 2602.12. | |
| Caerin 1.3 | Caerin 1.3 was found in Litoria caerula. Caerin 1.3 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-1.4 | Caerin-1.4 was found in Litoria gilleni. Caerin-1.4 is an antibacterial and antiviral peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin 1.5 | Caerin 1.5 was found in Litoria caerula. Caerin 1.5 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-1.6 | Caerin 1.6 was found in Litoria chloris. Caerin 1.6 is an antimicrobial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. | |
| Caerin-1.7 | Caerin 1.7 was found in Litoria chloris. Caerin 1.7 is an antimicrobial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. | |
| Caerin-1.8 | Caerin 1.8 was found in Litoria chloris. Caerin 1.8 is an antimicrobial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. | |
| Caerin 1.9 | Caerin 1.9 was found in Litoria chloris. Caerin 1.9 is an antimicrobial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Synonyms: Caerin 1.9; NH2-Gly-Leu-Phe-Gly-Val-Leu-Gly-Ser-Ile-Ala-Lys-His-Val-Leu-Pro-His-Val-Val-Pro-Val-Ile-Ala-Glu-Lys-Leu-NH2. Molecular formula: C124H206N32O28. Mole weight: 2593.2. | |
| Caerin 21 | Caerin 21 was found in Litoria peronii. It has antibacterial activity. | |
| Caerin-2.1 | Caerin 2.1 was found in Litoria splendida. Caerin 2.1 is an antimicrobial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-2.2 | Caerin 2.2 was found in Litoria gilleni. Caerin 2.2 is an antimicrobial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-2.4 | Caerin 2.4 was found in Litoria caerula. Caerin 2.4 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-2.5 | Caerin 2.5 was found in Litoria gilleni. Caerin 2.5 is an antimicrobial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin 2.6 | Caerin 2.6 was isolated from Hybrid between female Litoria splendida and male Litoria caerulea. It has antibacterial activity. | |
| Caerin 2.7 | Caerin 2.7 was isolated from Hybrid between female Litoria splendida and male Litoria caerulea. It has antibacterial activity. | |
| Caerin-3.2 | Caerin 3.2 was found in Litoria caerula. Caerin 3.2 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-3.3 | Caerin 3.3 was found in Litoria caerula. Caerin 3.3 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-3.4 | Caerin 3.4 was found in Litoria caerula. Caerin 3.4 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-3.5 | Caerin-3.5 was found in Litoria gracilenta. It shows significant activity against Gram-positive organisms, but is less effective against Gram-negative organisms. | |
| Caerin-4.1 | Caerin 4.1 was found in Litoria caerula. Caerin 4.1 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. Grades: >97% by HPLC. Molecular formula: C104H175N29O31. Mole weight: 2327.67. | |
| Caerin-4.2 | Caerin 4.2 was found in Litoria caerula. Caerin 4.2 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-4.3 | Caerin 4.3 was found in Litoria caerula. Caerin 4.3 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerulein, desulfated | Caerulein, desulfated is the desulfurated form of Caerulein. Caerulein, a CCK agonist, could be used in paralytic ileus and diagnostic aid in pancreatic malfunction. Synonyms: 4-Desulfocaerulein; H-Pyr-Gln-Asp-Tyr-Thr-Gly-Trp-Met-Asp-Phe-NH2; L-pyroglutamyl-L-glutaminyl-L-alpha-aspartyl-L-tyrosyl-L-threonyl-glycyl-L-tryptophyl-L-methionyl-L-alpha-aspartyl-L-phenylalaninamide; Pyr-QDYTGWMDF-NH2. Grades: >97% by HPLC. CAS No. 20994-83-6. Molecular formula: C58H73N13O18S. Mole weight: 1272.34. | |
| Caerulein precursor-related fragment Ea | The source of Caerulein precursor-related fragment Ea is Rana esculenta. This peptide has no sequence similarity with antimicrobial peptides isolated from other species of ranid frogs. It potently and selectively inhibits the growth of the Gram-positive bacterium Escherichia coli (minimal inhibitory concentration (MIC<5 microM)). Synonyms: CPRF-Ea. | |
| Caerulein precursor-related fragment Eb | The source of Caerulein precursor-related fragment Eb is Rana esculenta. This peptide has no sequence similarity with antimicrobial peptides isolated from other species of ranid frogs. It potently and selectively inhibits the growth of the Gram-positive bacterium Escherichia coli (minimal inhibitory concentration (MIC<5 microM)). Synonyms: CPRF-Eb. | |
| Caerulein precursor-related fragment Ec | The source of Caerulein precursor-related fragment Ec is Rana esculenta. This peptide has no sequence similarity with antimicrobial peptides isolated from other species of ranid frogs. It potently and selectively inhibits the growth of the Gram-positive bacterium Escherichia coli (minimal inhibitory concentration (MIC<5 microM)). Synonyms: CPRF-Ec. | |
| Caerulomycin | Caerulomycin is an antibiotic produced by Streptomyces caerleus and Nocadi-opsis cirriefficiens. It is mainly resistant to Gram-positive bacteria, yeast and mold (weak). Synonyms: Caerulomycin A. Grades: ≥98% by HPLC. CAS No. 21802-37-9. Molecular formula: C12H11N3O2. Mole weight: 229.23. | |
| Caerulomycin A | from Streptomyces caeruleus, ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Cafenstrole | Cafenstrole. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Cafenstrole, Cafenstrole [ISO], CID195429, 1H-1,2,4-Triazole-1-carboxamide, N,N-diethyl-3-mesitylsulfonyl-, N,N-Diethyl-3-mesitylsulfonyl-1H-1,2,4-triazole-1-carboxamide, 125306-83-4. Product Category: Heterocyclic Organic Compound. CAS No. 125306-83-4. Molecular formula: C16H22N4O3S. Mole weight: 350.44. Purity: 0.96. IUPACName: N,N-diethyl-3-(2,4,6-trimethylphenyl)sulfonyl-1,2,4-triazole-1-carboxamide. Canonical SMILES: CCN(CC)C(=O)N1C=NC(=N1)S(=O)(=O)C2=C(C=C(C=C2C)C)C. Density: 1.26g/cm³. ECNumber: 603-054-9. Product ID: ACM125306834. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cafenstrole | Cafenstrole. Group: Biochemicals. Grades: Highly Purified. CAS No. 125306-83-4. Pack Sizes: 5mg, 10mg, 25mg, 50mg. Molecular Formula: C16H22N4O3S. US Biological Life Sciences. | Worldwide |
| Cafestol | Cafestol is a natural bioactive substance isolated from the unsaponifiable fraction of petroleum ether extract of coffee beans, it acts as a GST (glutathione S-transferase) inducer and exhibits chemoprotective activity. Dietary cafestol does increase total cholesterol and triglycerides in ApoE3Leiden mice, an effect which is associated with selective activation of farnesoid X receptors and pregnane X receptors. Synonyms: cafestol; 469-83-0; cafesterol; CCRIS 1518; AC465T6Q6W; CHEBI:3291; (3bS,5aS,7R,8R,10aR,10bS)-7-(hydroxymethyl)-10b-methyl-3b,4,5,6,7,8,9,10,10a,10b,11,12-dodecahydro-5a,8-methanocyclohepta[5,6]naphtho[2,1-b]furan-7-ol. Grades: ≥98%. CAS No. 469-83-0. Molecular formula: C20H28O3. Mole weight: 316.4. | |
| Cafestol | Cafestol. Group: Biochemicals. Alternative Names: (3bS, 5aS, 7R, 8R, 10aR, 10bS)-3b, 4, 5, 6, 7, 8, 9, 10, 10a, 10b, 11, 12-Dodecahydro-7-hydroxy-10b-methyl-5a, 8-methano-5aH-cyclohepta[5, 6]naphtho[2, 1-b]furan-7-methanol; [3bS-(3bα,5a β,7 β,8 β,10aα,10b β)]-3b, 4, 5, 6, 7, 8, 9, 10, 10a, 10b, 11, 12-Dodecahydro-7-hydroxy-10b-methyl-5a, 8-methano-5aH-cyclohepta[5, 6]naphtho[2, 1-b]furan-7-methanol ; Cafesterol. Grades: Highly Purified. CAS No. 469-83-0. Pack Sizes: 50mg. Molecular Formula: C20H28O3, Molecular Weight: 316.43. US Biological Life Sciences. | Worldwide |
| Cafestol | Cafestol is an orally active diterpenoid and an inhibitor of ERK2. Cafestol has elevated blood lipids, anti-inflammatory, anti-angiogenic and anti-diabetic activities. In addition, Cafestol induces tumor cell apoptosis and autophagy , which can be used in the study of cancer [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. CAS No. 469-83-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 20 mg. Product ID: HY-N6257. | |
| caffeate 3,4-dioxygenase | This enzyme belongs to the family of oxidoreductases, specifically those acting on single donors with O2 as oxidant and incorporation of two atoms of oxygen into the substrate (oxygenases). The oxygen incorporated need not be derived from O2. The systematic name of this enzyme class is 3,4-dihydroxy-trans-cinnamate:oxygen 3,4-oxidoreductase (decyclizing). This enzyme participates in phenylpropanoid biodegradation. Group: Enzymes. Synonyms: 3,4-dihydroxy-trans-cinnamate:oxygen 3,4-oxidoreductase (decyclizing). Enzyme Commission Number: EC 1.13.11.22. CAS No. 37256-61-4. 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-0541; caffeate 3,4-dioxygenase; EC 1.13.11.22; 37256-61-4; 3,4-dihydroxy-trans-cinnamate:oxygen 3,4-oxidoreductase (decyclizing). Cat No: EXWM-0541. |  |
| caffeate CoA-transferase | The enzyme, isolated from the bacterium Acetobacterium woodii, catalyses an energy-saving CoA loop for caffeate activation. In addition to caffeate, the enzyme can utilize 4-coumarate or ferulate as CoA acceptor. Group: Enzymes. Synonyms: CarA. Enzyme Commission Number: EC 2.8.3.23. 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-3419; caffeate CoA-transferase; EC 2.8.3.23; CarA. Cat No: EXWM-3419. | |
| caffeate O-methyltransferase | 3,4-Dihydroxybenzaldehyde and catechol can act as acceptors, but more slowly. Group: Enzymes. Synonyms: caffeate methyltransferase; caffeate 3-O-methyltransferase; S-adenosyl-L-methionine:caffeic acid-O-methyltransferase. Enzyme Commission Number: EC 2.1.1.68. CAS No. 50936-45-3. 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-1969; caffeate O-methyltransferase; EC 2.1.1.68; 50936-45-3; caffeate methyltransferase; caffeate 3-O-methyltransferase; S-adenosyl-L-methionine:caffeic acid-O-methyltransferase. Cat No: EXWM-1969. | |
| Caffeic acid | Caffeic acid is an inhibitor of both TRPV1 ion channel and 5-Lipoxygenase ( 5-LO ). Uses: Scientific research. Group: Natural products. CAS No. 331-39-5. Pack Sizes: 10 mM * 1 mL; 5 g; 10 g; 25 g. Product ID: HY-N0172. | |
| Caffeic acid | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitespharma & vet compounds & metabolites. Alternative Names: 4-(2-Carboxyethenyl)-1,2-dihydroxybenzene, 3,4-Dihydroxybenzeneacrylic acid, Cinnamic acid, 3,4-dihydroxy- (8CI), 4-(2'-Carboxyvinyl)-1,2-dihydroxybenzene,3,4-Dihydroxycinnamic Acid, NSC 57197, Caffeic Acid, 3-(3,4-Dihydroxyphenyl)-2-propenoic acid, 3-(3,4-Dihydroxyphenyl)propenoic acid, NSC 623438. | |
| Caffeic acid | United States Pharmacopeia (USP) Reference Standard. Uses: For analytical and research use. Group: Pharmacopeia & metrological institutes standards; pharma & vet compounds & metabolites; pharma & vet compounds & metabolites. Alternative Names: 4-(2-Carboxyethenyl)-1,2-dihydroxybenzene, 3,4-Dihydroxybenzeneacrylic acid, Cinnamic acid, 3,4-dihydroxy- (8CI), 4-(2'-Carboxyvinyl)-1,2-dihydroxybenzene,3,4-Dihydroxycinnamic Acid, NSC 57197, Caffeic Acid, 3-(3,4-Dihydroxyphenyl)-2-propenoic acid, 3-(3,4-Dihydroxyphenyl)propenoic acid, NSC 623438. CAS No. 331-39-5. Pack Sizes: 15MG, 100MG. IUPAC Name: 3-(3,4-dihydroxyphenyl)prop-2-enoic acid. Molecular formula: C9H8O4. Mole weight: 180.16. Catalog: APS331395A. SMILES: OC(=O)C=Cc1ccc(O)c(O)c1. Format: Neat. Shipping: Room Temperature. | |
| Caffeic Acid | Caffeic Acid - Product ID: NST-10-5. Category: Hydroxycinnamic acids. Alternative Names: 3,4-Dihydroxycinnamic acid. Purity: 98%. Test method: HPLC. CAS No. 331-39-5. Pack Sizes: 50g, 100g, 250g, 500g. Appearance: White to slightly yellow Powder. Molecular formula: C9H8O4. Mole weight: 180.16. Storage: +2 +8 °C. |  |
| Caffeic Acid | Caffeic Acid is a constituent of plants, probably occurs in plants only in conjugated forms. Caffeic acid is found in all plants because it is a key intermediate in the biosynthesis of lignin, one of the principal sources of biomass. Caffeic acid is one of the main natural phenols in argan oi. Group: Biochemicals. Alternative Names: 3-(3,4-Dihydroxyphenyl)-2-propenoic Acid; 3,4-Dihydroxycinnamic Acid; 3, 4-Dihydroxy Benzene acrylic Acid; 3-(3,4-Dihydroxyphenyl)-2-propenoic Acid; 4-(2-Carboxyethenyl)-1,2-dihydroxybenzene; NSC 57197; NSC 623438. Grades: Highly Purified. CAS No. 331-39-5. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Caffeic Acid | Caffeic Acid. Synonyms: 3,4-Dihydroxybenzeneacrylic acid, 3,4-Dihydroxycinnamic acid, 3-(3,4-Dihydroxyphenyl)-2-propenoic acid. CAS No. 331-39-5. Pack Sizes: 2, 5, 25 g in poly bottle. Product ID: CDC10-0037. Molecular formula: C9H8O4. Category: Antioxidant Cosmetic Chemicals. Product Keywords: Cosmetic Ingredients; Antioxidant Cosmetic Chemicals; Caffeic Acid; CDC10-0037; 331-39-5; C9H8O4; 3,4-Dihydroxybenzeneacrylic acid, 3,4-Dihydroxycinnamic acid, 3-(3,4-Dihydroxyphenyl)-2-propenoic acid; 206-361-2; MFCD00004392; 331-39-5. Purity: ≥98.0% (HPLC). EC Number: 206-361-2. Physical State: Powder. Solubility: Soluble in DMSO (40 mg/mL), ethanol (25 mg/mL warm), DMF (~7 mg/mL), PBS, PH 7.2 (~0.65 mg/mL), hot water, ethyl acetate, Chloroform Hexane, and methanol. Application: Caffeic acid has been used as a standard of phenolic acid in the study to determine the total phenolic acid content in vegetables after subjecting to alkaline and acid hydrolysis. It has also been used to determine its antioxidant activity by various assay methods. Boiling Point: ~416.8° C at 760 mmHg (Predicted). Melting Point: 211-213 °C (dec.) (lit.). Density: ~1.5 g/cm3 (Predicted). Product Description: Caffeic acid exists in its free and ester form. It is considered as the predominant polyphenol, contributing to the hydroxycinnamic acid content in various fruits. Coffee is one of the major source of caffeic acid. |  |
| CAFFEIC ACID | CAFFEIC ACID. Group: other nano materials. Alternative Names: 4-(2-Carboxyethenyl)-1,2-dihydroxybenzene. CAS No. 331-39-5. Product ID: (E)-3-(3,4-Dihydroxyphenyl)prop-2-enoic acid. Molecular formula: 180.16. Mole weight: C9H8O4. C1=CC(=C(C=C1C=CC(=O)O)O)O. 98%. | |
| Caffeic acid 1,1-dimethylallyl ester | analytical standard. Group: Chemical class. | |
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