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| Product | Description | |
|---|---|---|
| chlorophyll | Synonyms: c.i.1956; chlorofolin; chlorofyl; Chlorophyl; chlorophylls; Chromule. Grades: 95%. CAS No. 1406-65-1. Molecular formula: C55H72MgN4O5. Mole weight: 893.48898. |  |
| CHLOROPHYLL | CHLOROPHYLL. Synonyms: c.i.1956; chlorofolin; chlorofyl; Chlorophyl; chlorophylls; Chromule; deodophyll. CAS No. 1406-65-1. Pack Sizes: 1 kg. Product ID: CDF4-0020. Molecular formula: C54H69MgN4O5R+2. Category: Color Fixative. Product Keywords: Food Ingredients; Color Fixative; CHLOROPHYLL; CDF4-0020; 1406-65-1; C54H69MgN4O5R+2; 215-800-7; 1406-65-1. Purity: 0.99. EC Number: 215-800-7. Application: chlorophyll is used as a natural coloring agent. It is credited with skin-soothing and healing properties thanks to its phytol content, and has a mild deodorizing effect. Chlorophyll is the green coloring matter found in all living plants and seen in plant leaves. |  |
| Chlorophyll a | Chlorophyll a. Group: Biochemicals. Alternative Names: Phorbine Magnesium Deriv.; Chlorophyll a; Chlorophyll-1; Magnesium Pheophytin; Vegetable Chlorophyll; α-Chlorophyll; (SP-4-2)-[(2E,7R,11R)-3,7,11,15-tetramethyl-2-hexadecenyl (3S, 4S, 21R)-9-ethenyl-14-ethyl-21-(methoxycarbonyl)-4, 8, 13, 18-tetramethyl-20-oxo-3-phorbinepropanoato(2-)-κN23, κN24, κN25, κN26]-Magnesium. Grades: Highly Purified. CAS No. 479-61-8. Pack Sizes: 1mg. Molecular Formula: C55H72MgN4O5, Molecular Weight: 893.49. US Biological Life Sciences. |  Worldwide |
| Chlorophyll a | Chlorophyll a is an important light-harvesting, green or blue color pigment present in the photosynthetic membranes of the chloroplasts in plant cells. CAS No. 479-61-8. Product ID: PE-0217. Molecular formula: C55H72MgN4O5. Mole weight: 893.49. Category: Colorant Excipients. Product Keywords: Pharmaceutical Excipients; Solid Dosage Form; Semi-solid Dosage Form; Suppository Bases; Colorant Excipients; Chlorophyll a; PE-0217; C55H72MgN4O5; 479-61-8; 479-61-8. Appearance: Powder. Purity: ≥85% (HPLC). EC Number: 207-536-6. Quality Level: 200. Storage: -20°C. | |
| Chlorophyll a | Chlorophyll a is a photosynthetic pigment required by eukaryotes and cyanobacteria for photosynthesis. It is the main donor of electron transport chain, and it is a dye and metabolite. Synonyms: Magnesium chlorophyll; Chlorophyll A; Chlorophyll-1; Magnesium Pheophytin; Vegetable Chlorophyll; α-Chlorophyll; (SP-4-2)-[(2E,7R,11R)-3,7,11,15-tetramethyl-2-hexadecenyl (3S, 4S, 21R)-9-ethenyl-14-ethyl-21-(methoxycarbonyl)-4, 8, 13, 18-tetramethyl-20-oxo-3-phorbinepropanoato(2-)-κN23, κN24, κN25, κN26]-Magnesium; Chlorophyll a, from spinach. Grades: 98%. CAS No. 479-61-8. Molecular formula: C55H72MgN4O5. Mole weight: 893.49. | |
| Chlorophyll a | Chlorophyll a is a plant extract. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 479-61-8. Pack Sizes: 1 mg. Product ID: HY-W127744. |  |
| Chlorophyll a | Colorant Standards. Uses: For analytical and research use. Group: Reagents. Grades: analytical standard. CAS No. 479-61-8. Pack Sizes: 1MG. |  |
| Chlorophyll a | Pharmacopeia & Metrological Institutes Standards. Uses: For analytical and research use. Group: Reagents. CAS No. 479-61-8. Pack Sizes: 15MG. | |
| Chlorophyll A | Chlorophyll A. Synonyms: chlorophyllafromspinach;Magnesium, (3, 7, 11, 15-tetramethyl-2-hexadecenyl9-ethenyl-14-ethyl-(methoxycarbonyl)-4, 8, 13, 18-tetramethyl-20-oxo-3-phorbinepropanoate(2-)-N23, N24, N25, N26)-(SP-4-2(3S-(3α(2E, 7S*, 11S*), 4β, 21β)))-;magnesium, [3, 7, 11, 15-tetramethyl-2-hexadecenyl9-ethenyl-14-ethyl-21-(methoxyc;Paste chlorophyll;Chlorophyll, paste;CONTAMINON(R) CL;CHLOROPHYLL EXTRACT;CHLOROPHYLL A. CAS No. 479-61-8. Pack Sizes: 10 mg, 25 mg, 50 mg, 100 mg. Product ID: CDF4-0024. Molecular formula: C55H72MgN4O5. Category: Color Fixative. Product Keywords: Food Ingredients; Color Fixative; Chlorophyll A; CDF4-0024; 479-61-8; C55H72MgN4O5; 207-536-6; 479-61-8. Purity: 0.999. Color: Green to Black Semi-Solid to. EC Number: 207-536-6. Physical State: Powder. Solubility: diethyl ether: soluble0.1mg/10 mL. Storage: -20°C. Application: Chlorophyll A is a photosynthetic pigment that is essential for photosynthesis of eukaryotes and cyanobacteria, acting as a primary donor in the electron transport chain. Dyes and metabolites. Melting Point: 117-120°. Product Description: Chlorophyll a is present as a key pigment in organisms with oxygenic photosynthesis. It functions as an antenna pigment in both reaction centers I and II. | |
| chlorophyllase | Chlorophyllase has been found in higher plants, diatoms, and in the green algae Chlorella. This enzyme forms part of the chlorophyll degradation pathway and is thought to take part in de-greening processes such as fruit ripening, leaf senescence and flowering, as well as in the turnover and homeostasis of chlorophyll. This enzyme acts preferentially on chlorophyll a but will also accept chlorophyll b and pheophytins as substrates. Ethylene and methyl jasmonate, which are known to accelerate senescence in many species, can enhance the activity of the hormone-inducible form of this enzyme. Group: Enzymes. Synonyms: CLH; Chlase. Enzyme Commission Number: EC 3.1.1.14. CAS No. 9025-96-1. 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-3441; chlorophyllase; EC 3.1.1.14; 9025-96-1; CLH; Chlase. Cat No: EXWM-3441. |  |
| Chlorophyll a (Technical Grade) | Dyes & Metabolites; Dyes & Metabolites. Uses: For analytical and research use. Group: Reagents. CAS No. 479-61-8. | |
| Chlorophyll b | Chlorophyll b is an orally active tetrapyrrole derivative and pigment. Chlorophyll b can be obtained from photosynthetic organisms such as plants and algae. Chlorophyll b acts as a hydrogen donor and increases Glutathione levels. Chlorophyll b has antioxidant activity and functionally replaces chlorophyll a in photosystem II to participate in photosynthesis. Chlorophyll b reduces Cisplatin (HY-17394)-induced DNA damage, chromosome instability, and oxidative stress. Chlorophyll b is mainly used in the study of plant photosynthesis mechanism [1] [2] [3]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 519-62-0. Pack Sizes: 500 μg. Product ID: HY-W127709. | |
| Chlorophyll b | Chlorophyll b is a photosynthetic pigment used in the absorption of light energy. Chlorophyl b is involved in photosynthesis and absorbs primarily blue light. Dyes and metabolites. Group: Biochemicals. Alternative Names: Phorbine, magnesium deriv.; Chlorophyll b; Chlorophyll-; β-Chlorophyll; (SP-4-2)-[(2E,7R,11R)-3,7,11,15-tetramethyl-2-hexadecenyl (3S, 4S, 21R)-9-ethenyl-14-ethyl-13-formyl-21-(methoxycarbonyl)-4, 8, 18-trimethyl-20-oxo-3-phorbinepropanoato(2-)-κN23, κN24, κN25, κN26]-Magnesium. Grades: Highly Purified. CAS No. 519-62-0. Pack Sizes: 1mg. Molecular Formula: C??H??MgN?O?, Molecular Weight: 907.47. US Biological Life Sciences. | Worldwide |
| Chlorophyllc3(sh) | Heterocyclic Organic Compound. CAS No. 111308-93-1. Molecular formula: C36H28MgN4O7. Mole weight: 652.94. Catalog: ACM111308931. |  |
| chlorophyllide a 31-hydratase | The enzyme, together with EC 1.3.7.15, chlorophyllide-a reductase, and EC 1.1.1.396, bacteriochlorophyllide-a dehydrogenase, is involved in the conversion of chlorophyllide a to bacteriochlorophyllide a. The enzymes can act in multiple orders, resulting in the formation of different intermediates, but the final product of the cumulative action of the three enzymes is always bacteriochlorophyllide a. The enzyme catalyses the hydration of a vinyl group on ring A, converting it to a hydroxyethyl group. Group: Enzymes. Synonyms: bchF (gene name). Enzyme Commission Number: EC 4.2.1.165. 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-5006; chlorophyllide a 31-hydratase; EC 4.2.1.165; bchF (gene name). Cat No: EXWM-5006. | |
| chlorophyllide a hydrolase | This enzyme, found in green sulfur bacteria (Chlorobiaceae) and green filamentous bacteria (Chloroflexaceae), catalyses the first committed step in the biosynthesis of bacteriochlorophylls c, d and e, the removal of the C-132-methylcarboxyl group from chlorophyllide a. The reaction is very similar to the conversion of pheophorbide a to pyropheophorbide a during chlorophyll a degradation, which is catalysed by EC 3.1.1.82, pheophorbidase. Group: Enzymes. Synonyms: bciC (gene name). Enzyme Commission Number: EC 3.1.1.100. 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-3436; chlorophyllide a hydrolase; EC 3.1.1.100; bciC (gene name). Cat No: EXWM-3436. | |
| chlorophyllide-a oxygenase | Chlorophyll b is required for the assembly of stable light-harvesting complexes (LHCs) in the chloroplast of green algae, cyanobacteria and plants. Contains a mononuclear iron centre. The enzyme catalyses two successive hydroxylations at the 7-methyl group of chlorophyllide a. The second step yields the aldehyde hydrate, which loses H2O spontaneously to form chlorophyllide b. Chlorophyll a and protochlorophyllide a are not substrates. Group: Enzymes. Synonyms: chlorophyllide a oxygenase; chlorophyll-b synthase; CAO. Enzyme Commission Number: EC 1.14.13.122. CAS No. 216503-73-0. 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-0723; chlorophyllide-a oxygenase; EC 1.14.13.122; 216503-73-0; chlorophyllide a oxygenase; chlorophyll-b synthase; CAO. Cat No: EXWM-0723. | |
| chlorophyllide a reductase | The enzyme, together with EC 1.1.1.396, bacteriochlorophyllide-a dehydrogenase, and EC 4.2.1.165, chlorophyllide-a 31-hydratase, is involved in the conversion of chlorophyllide a to bacteriochlorophyllide a. These enzymes can act in multiple orders, resulting in the formation of different intermediates, but the final product of the cumulative action of the three enzymes is always bacteriochlorophyllide a. This enzyme catalyses a trans-reduction of the B-ring; the product has the (7R,8R)-configuration. In addition, the enzyme has a latent activity of EC 1.3.7.13, 3,8-divinyl protochlorophyllide a 8-vinyl-reductase (ferredoxin). The enzyme contains a [4Fe-4S] cluster, and structurally resembles the Fe protein/MoFe protein complex of nitrogenase (EC 1.18.6.1), which catalyses an ATP-driven reduction. Group: Enzymes. Synonyms: bchX (gene name); bchY (gene name); bchZ (gene name); COR. Enzyme Commission Number: EC 1.3.7.15. 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-1396; chlorophyllide a reductase; EC 1.3.7.15; bchX (gene name); bchY (gene name); bchZ (gene name); COR. Cat No: EXWM-1396. | |
| chlorophyll(ide) b reductase | This enzyme carries out the first step in the conversion of chlorophyll b to chlorophyll a. It is involved in chlorophyll degradation, which occurs during leaf senescence and it also forms part of the chlorophyll cycle, which interconverts chlorophyll a and b in response to changing light conditions. Group: Enzymes. Synonyms: chlorophyll b reductase; Chl b reductase. Enzyme Commission Number: EC 1.1.1.294. 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-0203; chlorophyll(ide) b reductase; EC 1.1.1.294; chlorophyll b reductase; Chl b reductase. Cat No: EXWM-0203. | |
| Chlorophyllin Copper Trisodium Salt | Chlorophyllin Copper Trisodium Salt, is a water soluble derivative of Chlorophyll, which has shown to have has been shown to have both anticarcinogenic and antigenotoxic properties. Group: Biochemicals. Alternative Names: (SP-4-2)-[(7S, 8S)-3-Carboxy-5-(carboxymethyl)-13-ethenyl-18-ethyl-7, 8-dihydro-2, 8, 12, 17-tetramethyl-21H, 23H-porphine-7-propanoato(5-)-κN21, κN22, κN23, κN24]cuprate(3-) Sodium (1:3); Chlorine e6 Copper Deriv. Trisodium Salt; Chlorophyllin Copper Sodium Complex; PM 01-03B; Rovisome I; Sodium-copper Chlorin e6. Grades: Technical Grade. CAS No. 11006-34-1. Pack Sizes: 25g. Molecular Formula: C??H??CuN?Na?O?, Molecular Weight: 724.15. US Biological Life Sciences. | Worldwide |
| Chlorophyllin sodium copper salt | Chlorophyllin sodium copper salt. Synonyms: Chlorophyllin, coppered trisodium salt. CAS No. 11006-34-1. Pack Sizes: 5, 25, 100 g in glass bottle. Product ID: CDC10-0144. Molecular formula: C34H31CuN4Na3O6. Category: Cosmetic Color Additives. Product Keywords: Cosmetic Ingredients; Cosmetic Color Additives; Chlorophyllin sodium copper salt; CDC10-0144; 11006-34-1; C34H31CuN4Na3O6; Chlorophyllin, coppered trisodium salt; 234-242-5; 11006-34-1. Grade: commercial grade. Purity: 0.99. Color: Dark Green to Black. EC Number: 234-242-5. Physical State: Powder. Solubility: H2O: 100 mg/mL, dark green. Quality Level: 200. Storage: 2-8°C. Application: Chlorophyllin sodium copper salt has been used to study the effect of chlorophyllin against radiation-induced hematopoietic syndrome. It has been used to study the effect of chlorophyllin on the excretion of PhIP (2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine) and its metabolites into the breast-milk of lactating rats. Boiling Point: N/A. Melting Point: >300°C. | |
| Chlorophyllin sodium copper salt | Heterocyclic Organic Compound. Alternative Names: Chlorophyllin, coppered trisodium salt. CAS No. 11006-34-1. Molecular formula: C34H31CuN4Na3O6. Mole weight: 724.15. Appearance: Green to Very Dark Green and Black powder. Catalog: ACM11006341. | |
| chlorophyll synthase | Requires Mg2+. The enzyme is modified by binding of the first substrate, phytyl diphosphate, before reaction of the modified enzyme with the second substrate, chlorophyllide a, can occur. The reaction also occurs when phytyl diphosphate is replaced by geranylgeranyl diphosphate. Group: Enzymes. Enzyme Commission Number: EC 2.5.1.62. CAS No. 9077-8-1. 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-2800; chlorophyll synthase; EC 2.5.1.62; 9077-08-1. Cat No: EXWM-2800. | |
| 3,8-divinyl chlorophyllide a reductase | The enzyme, found only in bacteriochlorophyll b-producing bacteria, catalyses the introduction of a C-8 ethylidene group. The enzyme contains a [4Fe-4S] cluster, and structurally resembles the Fe protein/MoFe protein complex of nitrogenase. It is very similar to EC 1.3.7.15, chlorophyllide a reductase, and is composed of three subunits. Two of them form the catalytic component, while the third one functions as an ATP-dependent reductase component that catalyses the electron transfer from ferredoxin to the catalytic component. Group: Enzymes. Enzyme Commission Number: EC 1.3.7.14. 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-1395; 3,8-divinyl chlorophyllide a reductase; EC 1.3.7.14. Cat No: EXWM-1395. | |
| 3,8-divinyl protochlorophyllide a 8-vinyl-reductase (ferredoxin) | The enzyme, found in many phototrophic bacteria, land plants, and some green and red algae, is involved in the production of monovinyl versions of (bacterio)chlorophyll pigments from their divinyl precursors. Binds two [4Fe-4S] clusters and an FAD cofactor. It can also act on 3,8-divinyl chlorophyllide a, 3,8-divinyl chlorophyll a, and chlorophyll c2. cf. EC 1.3.1.75, 3,8-divinyl protochlorophyllide a 8-vinyl-reductase (NADPH). Group: Enzymes. Synonyms: bciB (gene name); cyano-type divinyl chlorophyllide a 8-vinyl-reductase. Enzyme Commission Number: EC 1.3.7.13. 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-1394; 3,8-divinyl protochlorophyllide a 8-vinyl-reductase (ferredoxin); EC 1.3.7.13; bciB (gene name); cyano-type divinyl chlorophyllide a 8-vinyl-reductase. Cat No: EXWM-1394. | |
| 3,8-divinyl protochlorophyllide a 8-vinyl-reductase (NADPH) | The enzyme, found in higher plants, green algae, and some phototrophic bacteria, is involved in the production of monovinyl versions of (bacterio)chlorophyll pigments from their divinyl precursors. It can also act on 3,8-divinyl chlorophyllide a. cf. EC 1.3.7.13, 3,8-divinyl protochlorophyllide a 8-vinyl-reductase (ferredoxin). Group: Enzymes. Synonyms: DVR (gene name); bciA (gene name); [4-vinyl]chlorophyllide a reductase; 4VCR; chlorophyllide-a:NADP+ oxidoreductase; divinyl chlorophyllide a 8-vinyl-reductase; plant-type divinyl chlorophyllide a 8-vinyl-reductase. Enzyme Commission Number: EC 1.3.1.75. 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-1344; 3,8-divinyl protochlorophyllide a 8-vinyl-reductase (NADPH); EC 1.3.1.75; DVR (gene name); bciA (gene name); [4-vinyl]chlorophyllide a reductase; 4VCR; chlorophyllide-a:NADP+ oxidoreductase; divinyl chlorophyllide a 8-vinyl-reductase; plant-type divinyl chlorophyllide a 8-vinyl-reductase. Cat No: EXWM-1344. | |
| 7-hydroxymethyl chlorophyll a reductase | Contains FAD and an iron-sulfur center. This enzyme, which is present in plant chloroplasts, carries out the second step in the conversion of chlorophyll b to chlorophyll a (cf. EC 1.1.1.294, chlorophyll(ide) b reductase). It similarly reduces chlorophyllide a. Group: Enzymes. Synonyms: HCAR. Enzyme Commission Number: EC 1.17.7.2. 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-1097; 7-hydroxymethyl chlorophyll a reductase; EC 1.17.7.2; HCAR. Cat No: EXWM-1097. | |
| Aluminum, chlorophyll complexes | Heterocyclic Organic Compound. Alternative Names: Aluminum, chlorophyll complexes;Einecs 309-256-0. CAS No. 100208-54-6. Catalog: ACM100208546. | |
| bacteriochlorophyllide a dehydrogenase | The enzyme, together with EC 1.3.7.15, chlorophyllide-a reductase, and EC 4.2.1.165, chlorophyllide-a 31-hydratase, is involved in the conversion of chlorophyllide a to bacteriochlorophyllide a. The enzymes can act in multiple orders, resulting in the formation of different intermediates, but the final product of the cumulative action of the three enzymes is always bacteriochlorophyllide a. The enzyme oxidizes a hydroxyl group on ring A, converting it to an oxo group. Group: Enzymes. Synonyms: bchC (gene name). Enzyme Commission Number: EC 1.1.1.396. 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-0316; bacteriochlorophyllide a dehydrogenase; EC 1.1.1.396; bchC (gene name). Cat No: EXWM-0316. | |
| Bacteriochlorophylls a | Bacteriochlorophylls a is produced by the strain of Chlorobiea and Rhodospirillinea. It has a structural skeleton similar to chlorophyll of higher plants. Synonyms: Bacteriochlorophyll; C11242. Grades: ≥95%. CAS No. 17499-98-8. Molecular formula: C55H74MgN4O6. Mole weight: 911.50. | |
| Bacteriochlorophylls b | Bacteriochlorophylls b is produced by the strain of Chlorobiea and Rhodospirillinea. It has a structural skeleton similar to chlorophyll of higher plants. Molecular formula: C55H72MgN4O6. Mole weight: 909.49. | |
| red chlorophyll catabolite reductase | The enzyme participates in chlorophyll degradation, which occurs during leaf senescence and fruit ripening in higher plants. The reaction requires reduced ferredoxin, which is generated from NADPH produced either through the pentose-phosphate pathway or by the action of photosystem I. This reaction takes place while red chlorophyll catabolite is still bound to EC 1.14.15.17, pheophorbide a oxygenase. Depending on the plant species used as the source of enzyme, one of two possible C-1 epimers of primary fluorescent chlorophyll catabolite (pFCC), pFCC-1 or pFCC-2, is normally formed, with all genera or species within a family producing the same isomer. After modification and export, pFCCs are eventually imported into the vacuole, where the acidic environment causes their non-enzymic conversion into colourless breakdown products called non-fluorescent chlorophyll catabolites (NCCs). Group: Enzymes. Synonyms: RCCR; RCC reductase; red Chl catabolite reductase. Enzyme Commission Number: EC 1.3.7.12. 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-1393; red chlorophyll catabolite reductase; EC 1.3.7.12; RCCR; RCC reductase; red Chl catabolite reductase. Cat No: EXWM-1393. | |
| Sodium copper chlorophyllin | A water-soluble Copper Trisodium Salt form of Chlorophyllin which could be used as a food additive and medicine of it has been proved to exert antioxidant and potential anticarcinogenic properties. Nutritional supplement in health care products. Uses: Ingredient of health care products. Synonyms: Cuprate(3-), [(7S, 8S)-3-carboxy-5-(carboxymethyl)-13-ethenyl-18-ethyl-7, 8-dihydro-2, 8, 12, 17-tetramethyl-21H, 23H-porphine-7-propanoato(5-)-κN21, κN22, κN23, κN24]-, sodium (1:3), (SP-4-2)-; Chlorophyllin Sodium Copper; Chlorophyllide Cu complex sodium salt; Chlorophyllin sodium copper salt; Chlorine e6, copper deriv., trisodium salt; Chlorophyllin, copper sodium complex; Cuprate(3-), [(7S, 8S)-3-carboxy-5-(carboxymethyl)-13-ethenyl-18-ethyl-7, 8-dihydro-2, 8, 12, 17-tetramethyl-21H, 23H-porphine-7-propanoato(5-)-κN21, κN22, κN23, κN24]-, trisodium, (SP-4-2)-; Chloron; Chloron G; Chlorophyllin copper complex sodium; Chlorophyllin coppered trisodium salt; Copper chlorophyllin a trisodium salt; JPM 01-03B; Rovisome I; Sodium-copper chlorin e6. Grades: 95%. CAS No. 11006-34-1. Molecular formula: C34H31CuN4Na3O6. Mole weight: 724.15. | |
| 2-[(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)acetyl]-butanedioic-2-13C Acid Diethyl Ester | 2-[(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)acetyl]-butanedioic-2-13C Acid Diethyl Ester is an intermediate in the synthesis of 5-Aminolevulinic Acid-3-13C Hydrochloride which is a naturally occurring amino acid; precursor of tetrapyrroles in the biosynthesis of chlorophyll and heme. Antineoplastic (photosensitizer). Group: Biochemicals. Grades: Highly Purified. CAS No. 123253-97-4. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C1713CH19NO7, Molecular Weight: 362.34. US Biological Life Sciences. | Worldwide |
| 2-[(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)acetyl]-butanedioic Acid Diethyl Ester | 2-[(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)acetyl]-butanedioic Acid Diethyl Ester is an intermediate in the synthesis of 5-Aminolevulinic Acid-3-13C Hydrochloride which is a naturally occurring amino acid; precursor of tetrapyrroles in the biosynthesis of chlorophyll and heme. Antineoplastic (photosensitizer). Group: Biochemicals. Grades: Highly Purified. CAS No. 2086325-07-5. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C18H19NO7, Molecular Weight: 361.35. US Biological Life Sciences. | Worldwide |
| 2-(1,3-Dioxoisoindolin-2-yl)acetyl Chloride | 2-(1,3-Dioxoisoindolin-2-yl)acetyl Chloride is an intermediate in the synthesis of 5-Aminolevulinic Acid-3-13C Hydrochloride which is a naturally occurring amino acid; precursor of tetrapyrroles in the biosynthesis of chlorophyll and heme. Antineoplastic (photosensitizer). Group: Biochemicals. Grades: Highly Purified. CAS No. 6780-38-7. Pack Sizes: 10mg, 25mg. Molecular Formula: C10H6ClNO3. US Biological Life Sciences. | Worldwide |
| 2-[2-(2,2-Dimethyl-4,6-dioxo-1,3-dioxan-5-yl)-2-oxoethyl]-1H-Isoindole-1,3(2H)-dione | 2-[2-(2,2-Dimethyl-4,6-dioxo-1,3-dioxan-5-yl)-2-oxoethyl]-1H-Isoindole-1,3(2H)-dione is an intermediate in the synthesis of 5-Aminolevulinic Acid-3-13C Hydrochloride which is a naturally occurring amino acid; precursor of tetrapyrroles in the biosynthesis of chlorophyll and heme. Antineoplastic (photosensitizer). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 10mg. Molecular Formula: C16H13NO7. US Biological Life Sciences. | Worldwide |
| 3- (Dimethylamino) acrolein | 3- (Dimethylamino) acrolein is used in the syntheses of benzochlorins, benzoisobacteriochlori ns, and benzobacteriochlorins. It is also used to prepare styryl-substituted Z/E-chlorin derivatives with chlorophyll-a skeleton. Group: Biochemicals. Grades: Highly Purified. CAS No. 927-63-9. Pack Sizes: 5g, 25g. Molecular Formula: C5H9NO, Molecular Weight: 99.13. US Biological Life Sciences. | Worldwide |
| 5,10,15,20-Tetra(4-pyridyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetra(4-pyridyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexesphthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetra(4-pyridyl)-21H,23H-porphine. CAS No. 16834-13-2. Pack Sizes: 1G-Glass Bottle with Plastic Insert. Product ID: 5,10,15,20-tetrapyridin-4-yl-21,23-dihydroporphyrin. Molecular formula: 618.7. Mole weight: C40H26N8. C1=CC2=C (C3=NC (=C (C4=CC=C (N4) C (=C5C=CC (=N5) C (=C1N2) C6=CC=NC=C6) C7=CC=NC=C7) C8=CC=NC=C8) C=C3) C9=CC=NC=C9. DNZSHSJERXNJGX-UHFFFAOYSA-N. InChI=1S/C40H26N8/c1-2-30-38 (26-11-19-42-20-12-26)32-5-6-34 (47-32)40 (28-15-23-44-24-16-28)36-8-7-35 (48-36)39 (27-13-21-43-22-14-27)33-4-3-31 (46-33)37 (29 (1)45-30)25-9-17-41-18-10-25/h1-24, 45, 48H. >93.0%(HPLC). |  |
| 5,10,15,20-Tetra(4-pyridyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetra(4-pyridyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Organic & printed electronics. Alternative Names: 5,10,15,20-Tetra(4-pyridyl)-21H,23H-porphine. CAS No. 16834-13-2. Molecular formula: C40H26N8. Mole weight: 618.7. Appearance: Gray to Dark purple to Black powder to crystal. Purity: >93.0%(HPLC). IUPACName: 5,10,15,20-tetrapyridin-4-yl-21,23-dihydroporphyrin. Canonical SMILES: C1=CC2=C (C3=NC (=C (C4=CC=C (N4) C (=C5C=CC (=N5) C (=C1N2) C6=CC=NC=C6) C7=CC=NC=C7) C8=CC=NC=C8) C=C3) C9=CC=NC=C9. Density: 1.335±0.06 g/cm3(Predicted). ECNumber: 240-858-5. Catalog: ACM16834132-2. | |
| 5,10,15,20-Tetrakis(2,6-dichlorophenyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis(2,6-dichlorophenyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Heterocyclic organic compound. Alternative Names: 5,10,15,20-Tetrakis(2,6-dichlorophenyl)porphine. CAS No. 37083-37-7. Molecular formula: C44H22Cl8N4. Mole weight: 890.29. Appearance: Green to Dark green to Dark blue powder to crystal. Purity: >95.0%(HPLC). IUPACName: 5,10,15,20-tetrakis(2,6-dichlorophenyl)-21,23-dihydroporphyrin. Canonical SMILES: C1=CC (=C (C (=C1)Cl)C2=C3C=CC (=C (C4=NC (=C (C5=CC=C (N5)C (=C6C=CC2=N6)C7=C (C=CC=C7Cl)Cl)C8=C (C=CC=C8Cl)Cl)C=C4)C9=C (C=CC=C9Cl)Cl)N3)Cl. Catalog: ACM37083377. | |
| 5,10,15,20-Tetrakis(2,6-dichlorophenyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis(2,6-dichlorophenyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexesphthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetrakis(2,6-dichlorophenyl)porphine. CAS No. 37083-37-7. Pack Sizes: 100MG-Glass Bottle with Plastic Insert. Product ID: 5,10,15,20-tetrakis(2,6-dichlorophenyl)-21,23-dihydroporphyrin. Molecular formula: 890.29. Mole weight: C44H22Cl8N4. C1=CC (=C (C (=C1)Cl)C2=C3C=CC (=C (C4=NC (=C (C5=CC=C (N5)C (=C6C=CC2=N6)C7=C (C=CC=C7Cl)Cl)C8=C (C=CC=C8Cl)Cl)C=C4)C9=C (C=CC=C9Cl)Cl)N3)Cl. InChI=1S/C44H22Cl8N4/c45-21-5-1-6-22 (46)37 (21)41-29-13-15-31 (53-29)42 (38-23 (47)7-2-8-24 (38)48)33-17-19-35 (55-33)44 (40-27 (51)11-4-12-28 (40)52)36-20-18-34 (56-36)43 (32-16-14-30 (41)54-32)39-25 (49)9-3-10-26 (39)50/h1-20, 53, 56H. UQASJTNIEXIESH-UHFFFAOYSA-N. >95.0%(HPLC). | |
| 5,10,15,20-Tetrakis(3,5-dihydroxyphenyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis(3,5-dihydroxyphenyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Heterocyclic organic compound. Alternative Names: 5,10,15,20-Tetrakis(3,5-dihydroxyphenyl)-21H,23H-porphine. CAS No. 145764-54-1. Molecular formula: C44H30N4O8. Mole weight: 742.74. Appearance: Dark red to Dark purple to Dark blue powder to crystal. Purity: >90.0%(HPLC). IUPACName: 5-[10,15,20-tris(3,5-dihydroxyphenyl)-21,24-dihydroporphyrin-5-yl]benzene-1,3-diol. Canonical SMILES: C1=CC2=C (C3=NC (=C (C4=CC=C (N4)C (=C5C=CC (=N5)C (=C1N2)C6=CC (=CC (=C6)O)O)C7=CC (=CC (=C7)O)O)C8=CC (=CC (=C8)O)O)C=C3)C9=CC (=CC (=C9)O)O. Density: 1.554g/cm³. Catalog: ACM145764541. | |
| 5,10,15,20-Tetrakis(3,5-dihydroxyphenyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis(3,5-dihydroxyphenyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexesphthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetrakis(3,5-dihydroxyphenyl)-21H,23H-porphine. CAS No. 145764-54-1. Product ID: 5-[10,15,20-tris(3,5-dihydroxyphenyl)-21,24-dihydroporphyrin-5-yl]benzene-1,3-diol. Molecular formula: 742.74. Mole weight: C44H30N4O8. C1=CC2=C (C3=NC (=C (C4=CC=C (N4)C (=C5C=CC (=N5)C (=C1N2)C6=CC (=CC (=C6)O)O)C7=CC (=CC (=C7)O)O)C8=CC (=CC (=C8)O)O)C=C3)C9=CC (=CC (=C9)O)O. InChI=1S/C44H30N4O8/c49-25-9-21 (10-26 (50)17-25)41-33-1-2-34 (45-33)42 (22-11-27 (51)18-28 (52)12-22)36-5-6-38 (47-36)44 (24-15-31 (55)20-32 (56)16-24)40-8-7-39 (48-40)43 (37-4-3-35 (41)46-37)23-13-29 (53)19-30 (54)14-23/h1-20, 45, 48-56H. XDVQXKKXBXLGCO-UHFFFAOYSA-N. >90.0%(HPLC). | |
| 5,10,15,20-Tetrakis(3,5-dimethoxyphenyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis(3,5-dimethoxyphenyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Heterocyclic organic compound. Alternative Names: 5,10,15,20-Tetrakis(3,5-dimethoxyphenyl)-21H,23H-porphine. CAS No. 74684-34-7. Molecular formula: C52H46N4O8. Mole weight: 854.96. Appearance: Dark red to Dark purple to Dark blue powder to crystal. Purity: >95.0%(HPLC). IUPACName: 5,10,15,20-tetrakis(3,5-dimethoxyphenyl)-21,23-dihydroporphyrin. Canonical SMILES: COC1=CC (=CC (=C1)C2=C3C=CC (=C (C4=NC (=C (C5=CC=C (N5)C (=C6C=CC2=N6)C7=CC (=CC (=C7)OC)OC)C8=CC (=CC (=C8)OC)OC)C=C4)C9=CC (=CC (=C9)OC)OC)N3)OC. Catalog: ACM74684347. | |
| 5,10,15,20-Tetrakis(3,5-dimethoxyphenyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis(3,5-dimethoxyphenyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexesphthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetrakis(3,5-dimethoxyphenyl)-21H,23H-porphine. CAS No. 74684-34-7. Product ID: 5,10,15,20-tetrakis(3,5-dimethoxyphenyl)-21,23-dihydroporphyrin. Molecular formula: 854.96. Mole weight: C52H46N4O8. COC1=CC (=CC (=C1)C2=C3C=CC (=C (C4=NC (=C (C5=CC=C (N5)C (=C6C=CC2=N6)C7=CC (=CC (=C7)OC)OC)C8=CC (=CC (=C8)OC)OC)C=C4)C9=CC (=CC (=C9)OC)OC)N3)OC. InChI=1S/C52H46N4O8/c1-57-33-17-29 (18-34 (25-33)58-2)49-41-9-11-43 (53-41)50 (30-19-35 (59-3)26-36 (20-30)60-4)45-13-15-47 (55-45)52 (32-23-39 (63-7)28-40 (24-32)64-8)48-16-14-46 (56-48)51 (44-12-10-42 (49)54-44)31-21-37 (61-5)27-38 (22-31)62-6/h9-28, 53, 56H, 1-8H3. YNXRFPUCCCJMPX-UHFFFAOYSA-N. >95.0%(HPLC). | |
| 5,10,15,20-Tetrakis(4-hydroxyphenyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis(4-hydroxyphenyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexesphthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetrakis(4-hydroxyphenyl)-21H,23H-porphine. CAS No. 51094-17-8. Product ID: 4-[10,15,20-tris(4-hydroxyphenyl)-21,23-dihydroporphyrin-5-yl]phenol. Molecular formula: 678.75. Mole weight: C44H30N4O4. C1=CC (=CC=C1C2=C3C=CC (=C (C4=NC (=C (C5=CC=C (N5)C (=C6C=CC2=N6)C7=CC=C (C=C7)O)C8=CC=C (C=C8)O)C=C4)C9=CC=C (C=C9)O)N3)O. InChI=1S/C44H30N4O4/c49-29-9-1-25 (2-10-29)41-33-17-19-35 (45-33)42 (26-3-11-30 (50)12-4-26)37-21-23-39 (47-37)44 (28-7-15-32 (52)16-8-28)40-24-22-38 (48-40)43 (36-20-18-34 (41)46-36)27-5-13-31 (51)14-6-27/h1-24, 45, 48-52H. VFHDWGAEEDVVPD-UHFFFAOYSA-N. >95.0%(HPLC). | |
| 5,10,15,20-Tetrakis(4-hydroxyphenyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis(4-hydroxyphenyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Organic & printed electronics. Alternative Names: 5,10,15,20-Tetrakis(4-hydroxyphenyl)-21H,23H-porphine. CAS No. 51094-17-8. Molecular formula: C44H30N4O4. Mole weight: 678.75. Appearance: Gray to Dark purple to Black powder to crystal. Purity: >95.0%(HPLC). IUPACName: 4-[10,15,20-tris(4-hydroxyphenyl)-21,23-dihydroporphyrin-5-yl]phenol. Canonical SMILES: C1=CC (=CC=C1C2=C3C=CC (=C (C4=NC (=C (C5=CC=C (N5)C (=C6C=CC2=N6)C7=CC=C (C=C7)O)C8=CC=C (C=C8)O)C=C4)C9=CC=C (C=C9)O)N3)O. Catalog: ACM51094178. | |
| 5,10,15,20-Tetrakis(4-methoxyphenyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis(4-methoxyphenyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexes other materials phthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetrakis(4-methoxyphenyl)-21H,23H-porphine. CAS No. 22112-78-3. Product ID: 5,10,15,20-tetrakis(4-methoxyphenyl)-21,23-dihydroporphyrin. Molecular formula: 734.86. Mole weight: C48H38N4O4. COC1=CC=C (C=C1)C2=C3C=CC (=C (C4=NC (=C (C5=CC=C (N5)C (=C6C=CC2=N6)C7=CC=C (C=C7)OC)C8=CC=C (C=C8)OC)C=C4)C9=CC=C (C=C9)OC)N3. InChI=1S/C48H38N4O4/c1-53-33-13-5-29 (6-14-33)45-37-21-23-39 (49-37)46 (30-7-15-34 (54-2)16-8-30)41-25-27-43 (51-41)48 (32-11-19-36 (56-4)20-12-32)44-28-26-42 (52-44)47 (40-24-22-38 (45)50-40)31-9-17-35 (55-3)18-10-31/h5-28, 49, 52H, 1-4H3. PJOJZHHAECOAFH-UHFFFAOYSA-N. >97.0%(T)(HPLC). | |
| [5,10,15,20-Tetrakis(4-methoxyphenyl)porphyrinato]cobalt(II) | Alfa Chemistry offers [5,10,15,20-Tetrakis(4-methoxyphenyl)porphyrinato]cobalt(II) products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Magnetic metal complexesphthalocyanine dyes, porphyrin dyes. Alternative Names: [5,10,15,20-Tetrakis(4-methoxyphenyl)-21H,23H-porphinato]cobalt(II). CAS No. 28903-71-1. Product ID: cobalt(2+); 5,10,15,20-tetrakis(4-methoxyphenyl)porphyrin-22,23-diide. Molecular formula: 791.77. Mole weight: C48H36CoN4O4. COC1=CC=C (C=C1)C2=C3C=CC (=C (C4=CC=C ([N-]4)C (=C5C=CC (=N5)C (=C6C=CC2=N6)C7=CC=C (C=C7)OC)C8=CC=C (C=C8)OC)C9=CC=C (C=C9)OC)[N-]3. [Co+2]. QBCIMRXPMLWVML-UHFFFAOYSA-N. >96.0%(T). | |
| [5,10,15,20-Tetrakis(4-methoxyphenyl)porphyrinato]cobalt(II) | Alfa Chemistry offers [5,10,15,20-Tetrakis(4-methoxyphenyl)porphyrinato]cobalt(II) products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Organic & printed electronics. Alternative Names: [5,10,15,20-Tetrakis(4-methoxyphenyl)-21H,23H-porphinato]cobalt(II). CAS No. 28903-71-1. Molecular formula: C48H36CoN4O4. Mole weight: 791.77. Appearance: Dark red to Dark purple to Dark blue powder to crystal. Purity: >96.0%(T). IUPACName: cobalt(2+);5,10,15,20-tetrakis(4-methoxyphenyl)porphyrin-22,23-diide. Canonical SMILES: COC1=CC=C (C=C1)C2=C3C=CC (=C (C4=CC=C ([N-]4)C (=C5C=CC (=N5)C (=C6C=CC2=N6)C7=CC=C (C=C7)OC)C8=CC=C (C=C8)OC)C9=CC=C (C=C9)OC)[N-]3. [Co+2]. Catalog: ACM28903711. | |
| 5,10,15,20-Tetrakis[4-(per-O-methyl-α-cyclodextrin-6-yloxy)phenyl]porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis[4-(per-O-methyl-α-cyclodextrin-6-yloxy)phenyl]porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Supramolecular host materials. Alternative Names: 5,10,15,20-Tetrakis[4-(per-O-methyl-α-cyclodextrin-6-yloxy)phenyl]-21H,23H-porphine. Molecular formula: 5451.91. Mole weight: C256H398N4O120. | |
| 5,10,15,20-Tetrakis(pentafluorophenyl)porphyrin | Alfa Chemistry offers 5,10,15,20-Tetrakis(pentafluorophenyl)porphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexes other materials phthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetrakis(perfluorophenyl)porphyrin 5,10,15,20-Tetrakis(pentafluorophenyl)-21H,23H-porphine. CAS No. 25440-14-6. Pack Sizes: 100MG-Glass Bottle with Plastic Insert. Product ID: 5,10,15,20-tetrakis(2,3,4,5,6-pentafluorophenyl)-21,23-dihydroporphyrin. Molecular formula: 974.56. Mole weight: C44H10F20N4. C1=CC2=C (C3=NC (=C (C4=CC=C (N4)C (=C5C=CC (=N5)C (=C1N2)C6=C (C (=C (C (=C6F)F)F)F)F)C7=C (C (=C (C (=C7F)F)F)F)F)C8=C (C (=C (C (=C8F)F)F)F)F)C=C3)C9=C (C (=C (C (=C9F)F)F)F)F. InChI=1S/C44H10F20N4/c45-25-21 (26 (46)34 (54)41 (61)33 (25)53)17-9-1-2-10 (65-9)18 (22-27 (47)35 (55)42 (62)36 (56)28 (22)48)12-5-6-14 (67-12)20 (24-31 (51)39 (59)44 (64)40 (60)32 (24)52)16-8-7-15 (68-16)19 | |
| [5, 15-Bis (phenylethynyl) -10, 20-bis[ (triisopropylsilyl) ethynyl]porphyrinato]magnesium (II) | Alfa Chemistry offers [5, 15-Bis (phenylethynyl) -10, 20-bis[ (triisopropylsilyl) ethynyl]porphyrinato]magnesium (II) products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Donor materials. CAS No. 1397288-30-0. Molecular formula: C58H60MgN4Si2. Mole weight: 893.62. Appearance: Green to Dark green powder to crystal. Purity: >95.0%(HPLC). Catalog: ACM1397288300. | |
| [5, 15-Bis (phenylethynyl) -10, 20-bis[ (triisopropylsilyl) ethynyl]porphyrinato]magnesium (II) | Alfa Chemistry offers [5, 15-Bis (phenylethynyl) -10, 20-bis[ (triisopropylsilyl) ethynyl]porphyrinato]magnesium (II) products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Dye-sensitized solar cell (dssc) materials electronic materials organic solar cell (opv) materials phthalocyanine dyes, porphyrin dyes. CAS No. 1397288-30-0. Molecular formula: 893.62. Mole weight: C58H60MgN4Si2. >95.0%(HPLC). | |
| 5,15-Diphenylporphyrin | Alfa Chemistry offers 5,15-Diphenylporphyrin Chloride products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexesphthalocyanine dyes, porphyrin dyes. Alternative Names: 5,15-Diphenyl-21H,23H-porphine. CAS No. 22112-89-6. Product ID: 10,20-diphenyl-21,22-dihydroporphyrin. Molecular formula: 462.56. Mole weight: C32H22N4. C1=CC=C (C=C1)C2=C3C=CC (=CC4=CC=C (N4)C (=C5C=CC (=N5)C=C6C=CC2=N6)C7=CC=CC=C7)N3. InChI=1S/C32H22N4/c1-3-7-21 (8-4-1)31-27-15-11-23 (33-27)19-25-13-17-29 (35-25)32 (22-9-5-2-6-10-22)30-18-14-26 (36-30)20-24-12-16-28 (31)34-24/h1-20, 33, 35H. QIBKIAFNCVIIMG-UHFFFAOYSA-N. >90.0%(HPLC). | |
| 5-(4-CArboxyphenyl)-10,15,20-triphenylporphyrin | Alfa Chemistry offers 5-(4-Carboxyphenyl)-10,15,20-triphenylporphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Heterocyclic organic compound. Alternative Names: 5-(4-Carboxyphenyl)-10,15,20-triphenyl-21H,23H-porphine. CAS No. 95051-10-8. Molecular formula: C45H30N4O2. Mole weight: 658.76. Appearance: Dark purple powder to crystal. Purity: >98.0%(HPLC). IUPACName: 4-(10,15,20-triphenyl-21,23-dihydroporphyrin-5-yl)benzoic acid. Canonical SMILES: C1=CC=C (C=C1)C2=C3C=CC (=C (C4=NC (=C (C5=CC=C (N5)C (=C6C=CC2=N6)C7=CC=CC=C7)C8=CC=C (C=C8)C (=O)O)C=C4)C9=CC=CC=C9)N3. Catalog: ACM95051108-1. | |
| 5-(4-CArboxyphenyl)-10,15,20-triphenylporphyrin | Alfa Chemistry offers 5-(4-Carboxyphenyl)-10,15,20-triphenylporphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexes other materials phthalocyanine dyes, porphyrin dyes. Alternative Names: 5-(4-Carboxyphenyl)-10,15,20-triphenyl-21H,23H-porphine. CAS No. 95051-10-8. Product ID: 4-(10,15,20-triphenyl-21,23-dihydroporphyrin-5-yl)benzoic acid. Molecular formula: 658.76. Mole weight: C45H30N4O2. C1=CC=C (C=C1)C2=C3C=CC (=C (C4=NC (=C (C5=CC=C (N5)C (=C6C=CC2=N6)C7=CC=CC=C7)C8=CC=C (C=C8)C (=O)O)C=C4)C9=CC=CC=C9)N3. GZTMFXHPFNRUNU-UHFFFAOYSA-N. InChI=1S/C45H30N4O2/c50-45 (51)32-18-16-31 (17-19-32)44-39-26-24-37 (48-39)42 (29-12-6-2-7-13-29)35-22-20-33 (46-35)41 (28-10-4-1-5-11-28)34-21-23-36 (47-34)43 (30-14-8-3-9-15-30)38-25-27-40 (44)49-38/h1-27, 46, 49H, (H, 50, 51). >98.0%(HPLC). | |
| 5-(4-Methoxycarbonylphenyl)-10,15,20-triphenylporphyrin | Alfa Chemistry offers 5-(4-Methoxycarbonylphenyl)-10,15,20-triphenylporphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Ligands for functional metal complexes other materials phthalocyanine dyes, porphyrin dyes. Alternative Names: 5-(4-Carbomethoxyphenyl)-10,15,20-triphenylporphyrin 5-(4-Methoxycarbonylphenyl)-10,15,20-triphenyl-21H,23H-porphine. CAS No. 119730-06-2. Product ID: methyl 4-(10,15,20-triphenyl-21,23-dihydroporphyrin-5-yl)benzoate. Molecular formula: 672.79. Mole weight: C46H32N4O2. COC (=O) C1=CC=C (C=C1) C2=C3C=CC (=N3) C (=C4C=CC (=C (C5=NC (=C (C6=CC=C2N6) C7=CC=CC=C7) C=C5) C8=CC=CC=C8) N4) C9=CC=CC=C9. AUUXSDUVWMAVMR-UHFFFAOYSA-N. InChI=1S/C46H32N4O2/c1-52-46 (51)33-19-17-32 (18-20-33)45-40-27-25-38 (49-40)43 (30-13-7-3-8-14-30)36-23-21-34 (47-36)42 (29-11-5-2-6-12-29)35-22-24-37 (48-35)44 (31-15-9-4-10-16-31)39-26-28-41 (45)50-39/h2-28, 47, 50H, 1H3. >90.0%(HPLC). | |
| 5-Aminolevulinic Acid-3-13C Hydrochloride | Naturally occurring amino acid; precursor of tetrapyrroles in the biosynthesis of chlorophyll and heme. Antineoplastic (photosensitizer). Group: Biochemicals. Alternative Names: 5-Amino-4-oxopentanoic Acid-13C; Hydrochloride; δ-Aminolevulinic-13C Acid Hydrochloride; Aminolevulinic-13C Acid Hydrochloride; 5-ALA HCl-13C; Levulan-13C. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Barley Grass Juice Powder | Barley grass juice powder is made from young leaves of the barley grass. Barley grass juice powder contains extremely high levels of vitamins, minerals, enzymes, amino acids, chlorophyll - deteriorate. Barley grass powder thus contains very dense nutritional and healing properties in a concentrated form that is easily assimilated by our digestive system.Yesherb barley grass juice powder is processed with low temperature drying technology, extremely contained the untrients that can easily absorbed by people. Group: Others. Barley Grass Juice Powder; Hordeum Brevisubulatum (Trin.) Link. Cat No: EXTC-116. | |
| bilirubin oxidase | This enzyme belongs to the family of oxidoreductases, to be specific those acting on the CH-CH group of donor with oxygen as acceptor. The systematic name of this enzyme class is bilirubin:oxygen oxidoreductase. This enzyme is also called bilirubin oxidase M-1. This enzyme participates in porphyrin and chlorophyll metabolism. Group: Enzymes. Synonyms: bilirubin oxidase M-1. Enzyme Commission Number: EC 1.3.3.5. CAS No. 80619-01-8. Bilirubin Oxidase. 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-1379; bilirubin oxidase; EC 1.3.3.5; 80619-01-8; bilirubin oxidase M-1. Cat No: EXWM-1379. | |
| Bilirubin oxidase | Bilirubin oxidase (BOD) is a multi-copper oxidase that catalyzes the oxidation of bilirubin to biliverdin and reduces molecular oxygen to water. Bilirubin oxidase can participate in the metabolism of porphyrin and chlorophyll, and is widely used in biochemical research as a catalyst for oxygen reduction [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BOD. CAS No. 80619-01-8. Pack Sizes: 250 U; 500 U; 1000 U. Product ID: HY-P2888. | |
| Bilirubin oxidase from Microorganism | In enzymology, a bilirubin oxidase (EC 1.3.3.5) is an enzyme that catalyzes the chemical reaction:2 bilirubin + O2? 2 biliverdin + 2 H2O. Thus, the two substRates of this enzyme are bilirubin and O2, whereas its two products are biliverdin and H2O. This enzyme belongs to the family of oxidoreductases, to be specific those acting on the CH-CH group of donor with oxygen as acceptor. This enzyme participates in porphyrin and chlorophyll metabolism. Group: Enzymes. Synonyms: bilirubin oxidase M-1; bilirubin oxidase; EC 1.3.3.5; bilirubin: oxygen oxidoreductase. Enzyme Commission Number: EC 1.3.3.5. CAS No. 80619-01-8. Activity: >20U/mg. Storage: Store at -20°C. Form: Blue powder, lyophilized. Source: Microorganism. bilirubin oxidase M-1; bilirubin oxidase; EC 1.3.3.5; bilirubin: oxygen oxidoreductase; BOD. Cat No: NATE-1713. | |
| Chlorella Powder | Chlorella powder is made from the Chlorella, a unicellular green alga which belongs to ereen Algae phylum, Chlorella genera, it is one kind sphere unicellular freshwater algae, Yesherb chlorella powder is rich in protein, vitamin, mineral substance, dietary fiber, nucleic acid and chlorophyll, etc, which are all the essential nutrient to maintain and promote people health, especially the biological active substance glycoprotein. Group: Others. Chlorella Powder; Chlorella Vulgaris. Cat No: EXTC-117. | |
| Cobalt(II) Tetraphenylporphyrin | Alfa Chemistry offers Cobalt(II) Tetraphenylporphyrin products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: The porphyrin metal complexes are important in-vivo, because they are included in chlorophyll functioning photo absorption and photo electron transfer for photosynthesis, and also included in heme transporting oxygen in blood. in addition, porphyrinato metal complexes are useful for photoelectron functional materials, metal complex catalysts and molecular electrical conductors. Group: Magnetic metal complexesphthalocyanine dyes, porphyrin dyes. Alternative Names: 5,10,15,20-Tetraphenyl-21H,23H-porphine Cobalt(II) Cobalt(II) TPP CoTPP (meso-Tetraphenylporphinato)Cobalt(II) Cobalt(II) meso-Tetraphenylporphine. CAS No. 14172-90-8. Product ID: cobalt(2+); 5,10,15,20-tetraphenylporphyrin-22,24-diide. Molecular formula: 671.67. Mole weight: C44H28CoN4. C1=CC=C (C=C1) C2=C3C=CC (=C (C4=NC (=C (C5=CC=C ([N-]5) C (=C6C=CC2=N6) C7=CC=CC=C7) C8=CC=CC=C8) C=C4) C9=CC=CC=C9) [N-]3. [Co+2]. InChI=1S/C44H28N4. Co/c1-5-13-29 (14-6-1)41-33-21-23-35 (45-33)42 (30-15-7-2-8-16-30)37-25-27-39 (47-37)44 (32-19-11-4-12-20-32)40-28-26-38 (48-40)43 (31-17-9-3-10-18-31)36-24-22-34 (41)46-36; /h1-28H; /q-2; +2. LSZLYWSRWXFMOI-UHFFFAOYSA-N. >80.0%(HPLC). | |
| diferric-transferrin reductase | This enzyme belongs to the family of oxidoreductases, specifically those oxidizing metal ion with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is transferrin[Fe(II)]2:NAD+ oxidoreductase. Other names in common use include diferric transferrin reductase, NADH diferric transferrin reductase, and transferrin reductase. This enzyme participates in porphyrin and chlorophyll metabolism. Group: Enzymes. Synonyms: diferric transferrin reductase; NADH diferric transferrin reductase; transferrin reductase. Enzyme Commission Number: EC 1.16.1.2. CAS No. 105238-49-1. 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-1067; diferric-transferrin reductase; EC 1.16.1.2; 105238-49-1; diferric transferrin reductase; NADH diferric transferrin reductase; transferrin reductase. Cat No: EXWM-1067. | |
| geranylgeranyl diphosphate reductase | This enzyme also acts on geranylgeranyl-chlorophyll a. The reaction occurs in three steps. Which order the three double bonds are reduced is not known. Group: Enzymes. Synonyms: geranylgeranyl reductase; CHL P. Enzyme Commission Number: EC 1.3.1.83. 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-1352; geranylgeranyl diphosphate reductase; EC 1.3.1.83; geranylgeranyl reductase; CHL P. Cat No: EXWM-1352. | |
| glutamate-tRNA ligase | This enzyme belongs to the family of ligases, to be specific those forming carbon-oxygen bonds in aminoacyl-tRNA and related compounds. This enzyme participates in 3 metabolic pathways: glutamate metabolism, porphyrin and chlorophyll metabolism, and aminoacyl-trna biosynthesis. Group: Enzymes. Synonyms: glutamyl-tRNA synthetase; glutamyl-transfer ribonucleate synthetase; glutamyl-transfer RNA synthetase; glutamyl-transfer ribonucleic acid synthetase; glutamate-tRNA synthetase; glutamic acid translase. Enzyme Commission Number: EC 6.1.1.17. CAS No. 9068-76-2. 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-5648; glutamate-tRNA ligase; EC 6.1.1.17; 9068-76-2; glutamyl-tRNA synthetase; glutamyl-transfer ribonucleate synthetase; glutamyl-transfer RNA synthetase; glutamyl-transfer ribonucleic acid synthetase; glutamate-tRNA synthetase; glutamic acid translase. Cat No: EXWM-5648. | |
| (±)-Jasmonic acid | (±)-Jasmonic acid is an endogenous growth regulator closely related to plant resistance to abiotic stresses, used to activate defense responses to wounding, herbivory, and pathogen attacks. (±)-Jasmonic acid does not play an independent regulatory role, but works in a complex signaling network with other plant hormone signaling pathways. In addition, (±)-Jasmonic acid can also reduce chlorophyll levels in green and etiolated barley leaf segments and inhibit the elongation of rice seedlings [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 77026-92-7. Pack Sizes: 25 mg (2.38 M * 50 μL in Ethanol); 50 mg (2.38 M * 100 μL in Ethanol); 100 mg (2.38 M * 200 μL in Ethanol); 250 mg (2.38 M * 500 μL in Ethanol). Product ID: HY-122464. | |
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