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100g Pack Size. Group: Analytical Reagents, Biochemicals, Buffers. Formula: C6H17N3O7. CAS No. 3458-72-8. Prepack ID 78832124-100g. Molecular Weight 243.22. See USA prepack pricing.
AmmoniumCitrate
AmmoniumCitrate, Dibasic
Ammoniumcitrate dibasic
Ammoniumcitrate dibasic (CAS# 3012-65-5) is a useful research chemical. Synonyms: azane;2-hydroxypropane-1,2,3-tricarboxylic acid. Grades: > 99 %. CAS No. 3012-65-5. Molecular formula: C6H14N2O7. Mole weight: 226.18.
Ammoniumcitrate dibasic
Ammoniumcitrate dibasic. Synonyms: Ammonium hydrogencitrate, Citric acid ammonium salt, Diammonium hydrogen citrate. CAS No. 3012-65-5. Pack Sizes: 100, 500 g in poly bottle. Product ID: CDC10-0097. Molecular formula: C6H14N2O7. Category: Cosmetic Chelating Chemicals. Product Keywords: Cosmetic Ingredients; Cosmetic Chelating Chemicals; Ammoniumcitrate dibasic; CDC10-0097; 3012-65-5; C6H14N2O7; Ammonium hydrogencitrate, Citric acid ammonium salt, Diammonium hydrogen citrate; 221-146-3; MFCD00013068; 3012-65-5. Purity: 0.98. Color: White. EC Number: 221-146-3. Physical State: Solid. Solubility: H2O: 1 M at 20 °C, clear, colorless. Quality Level: 200. Storage: Store at 5°C to 30°C. Application: Ammoniumcitrate dibasic can be used as both carbon and nitrogen precursor to synthesize nitrogen-doped fluorescent carbon nanoparticles (CNPs) for the development of sensitive and selective sensors for picric acid detection. Solution form of ammoniumcitrate can also be used in leaching experiments to extract copper nanoparticles from waste printed circuit boards (WPCBs). Boiling Point: 100 °C(lit.). Melting Point: 185 °C (dec.)(lit.). Density: 1.22 g/mL at 20 °C.
Ammoniumcitrate dibasic
Ammoniumcitrate dibasic. Synonyms: Ammonium hydrogencitrate, Citric acid ammonium salt, Diammonium hydrogen citrate. CAS No. 7585-39-9. Pack Sizes: 100, 500 g in poly bottle. Product ID: CDC10-0099. Molecular formula: C42H70O35. Category: Cosmetic Chelating Chemicals. Product Keywords: Cosmetic Ingredients; Cosmetic Chelating Chemicals; Ammoniumcitrate dibasic; CDC10-0099; 7585-39-9; C42H70O35; Ammonium hydrogencitrate, Citric acid ammonium salt, Diammonium hydrogen citrate; 221-146-3; MFCD00013068; 7585-39-9. Purity: 0.98. Color: White. EC Number: 221-146-3. Physical State: Solid. Solubility: 1 M NaOH: 50 mg/mL. Quality Level: 200. Application: Ammoniumcitrate dibasic can be used as both carbon and nitrogen precursor to synthesize nitrogen-doped fluorescent carbon nanoparticles (CNPs) for the development of sensitive and selective sensors for picric acid detection. Solution form of ammoniumcitrate can also be used in leaching experiments to extract copper nanoparticles from waste printed circuit boards (WPCBs). Boiling Point: 844.96°C (rough estimate). Melting Point: 290-300 °C (dec.) (lit.). Density: 1.2296 g/cm3(rough estimate).
AmmoniumCitrate dibasic
AmmoniumCitrate, dibasic. Grades: Reagent. CAS No. 3012-65-5. Order Number: 1058.
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AmmoniumCitrate Dibasic
AMMONIUMCITRATE DIBASIC, ACS Reagent, crystalline, (Citric Acid, Diammonium Salt, DiammoniumCitrate), Formula: (NH4)2HC6H5O7. CAS No. 3012-65-5. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today!
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AmmoniumCitrate Dibasic
AmmoniumCitrate Dibasic. CAS Number: 3012-65-5. Grade: ACS. Packaging: Fiber Drum.
New Jersey NJ
AmmoniumCitrate, Dibasic, ACS
AmmoniumCitrate, Dibasic, ACS. Group: Biochemicals. Alternative Names: Dihydrogen ammoniumcitrate; Citric acid, diammonium salt; Ammonium hydrogen citrate. Grades: ACS Grade. CAS No. 3012-65-5. Pack Sizes: 100g, 500g, 1Kg, 2.5Kg. Molecular Formula: (NH4)2C6H6O7, Molecular Weight: 226.18. US Biological Life Sciences.
Worldwide
Ammoniumcitrate tribasic
Ammoniumcitrate tribasic. Group: Biochemicals. Grades: Highly Purified. CAS No. 3458-72-8. Pack Sizes: 250g, 500g, 1kg, 2kg, 5kg. Molecular Formula: C6H17N3O7. US Biological Life Sciences.
Worldwide
Ammonium iron(III) citrate
Ammonium iron(III) citrate (Ammonium ferric citrate), a physiological form of nonetransferrin-bound iron, induces intracellular iron overload to cause ferroptosis [1]. Ammonium iron(III) citrate can enhance protein production [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Ammonium ferric citrate; FAC. CAS No. 1185-57-5. Pack Sizes: 1 g. Product ID: HY-B1645.
100g Pack Size. Group: Analytical Reagents, Building Blocks, Catalysts, Organics. Formula: C6H11FeNO7+3. CAS No. 1185-57-5. Prepack ID 90021908-100g. See USA prepack pricing.
Ammonium iron (III) citrate (Green)
1kg Pack Size. Group: Biochemicals, Salts. Formula: C6H11FeNO7+3. CAS No. 1185-57-5. Prepack ID 17006179-1kg. See USA prepack pricing.
di-Ammonium hydrogen citrate
1kg Pack Size. Group: Buffers, Salts. Formula: C6H14N2O7. CAS No. 3012-65-5. Prepack ID 14624490-1kg. Molecular Weight 226.18. See USA prepack pricing.
Ferric ammoniumcitrate
Iron Complexes. Alternative Names: ,2,3-Propanetricarboxylic acid, 2-hydroxy-, ammonium iron(3+) salt. CAS No. 1185-57-5. Molecular formula: C6H8O7.x-Fe.x-H3N. Mole weight: 261.98. Appearance: Green or brown powder. Purity: 95%+. IUPACName: Azane;2-hydroxypropane-1,2,3-tricarboxylate;iron(3+). Canonical SMILES: C (C (=O)[O-])C (CC (=O)[O-]) (C (=O)[O-])O. N. [Fe+3]. Catalog: ACM1185575-1.
Ferric AmmoniumCitrate
Ferric AmmoniumCitrate, green
Ferric AmmoniumCitrate
Ferric AmmoniumCitrate. Group: Biochemicals. Alternative Names: Ammonium Iron [III] Citrate; Ammonium ferric citrate. Grades: Reagent Grade. CAS No. 1185-57-5. Pack Sizes: 100g, 250g, 500g, 1Kg. Molecular Formula: C6H8FeNO7, Molecular Weight: 261.97. US Biological Life Sciences.
Heterocyclic Organic Compound. Alternative Names: Ammonium iron(III) citrate; Ammonium Ferric Citrate; Citric acid iron ammonium; Ironandammoniumcit-rate; Amonium Iron(III) Citrate Supplement; IRON AMMONIUMCITRATE; Ammoniumironcitrate; AmmoniumFerricCitrateUsp; Ferricammoniumcitrae; Ferric. CAS No. 1185-57-6. Molecular formula: C6H8FeNO7. Mole weight: 261.975. Appearance: Ferric ammoniumcitrate is a yellowish brown to red solid with a faint odor of ammonia. Purity: 0.96. IUPACName: Ammonium ferric citrate. Density: 1.8 g/cm³ (20ºC). Catalog: ACM1185576.
Butamirate Citrate
Butamirate is a cough suppressant. A study found it to bind to the cough center in the medulla oblongata, more specifically the dextromethorphan-binding site in guinea pig brain with high affinity. As a 2-(2-diethylaminoethoxy)ethyl ester it is chemically related to oxeladin and pentoxyverine, which are in the same class. Synonyms: Butamirate citrate; diethyl[2-[2- (2-phenylbutyroyloxy) ethoxy]ethyl]ammonium dihydrogen citrate; Butamiratdihydrogencitrat; Abbott 36581; HH-197; 2-(2-diethylaminoethyloxy)ethyl 2-phenylbutanoate; 2-phenylbutyric acid 2-(2-diethylaminoethyloxy)ethyl ester; 2-[2-(. Grades: > 95%. CAS No. 18109-81-4. Molecular formula: C18H29NO3 C6H8O7. Mole weight: 370.44 192.13.
Human Factor XIII
Factor XIII is the zymogenic form of the glutaminyl-peptide g-glutamyl transferase factor XIIIa (fibrinoligase, plasma transglutaminase, fibrin stabilizing factor, E.C. 2.3.2.13). Factor XIII is unique among transamidases in that it is a zymogen in vivo. Factor XIII is found both extracellularly in plasma and intracellularly in platelets, megakaryocytes, monocytes, placenta, uterus, liver and prostrate tissues. Plasma factor XIII is synthesized in the liver and circulates as a tetramer (Mr=320,000), composed of 2 pairs of nonidentical subunits (A2B2). The intra-cellular forms are synthesized in the tissues where they reside as dimers (Mr=146,000) of 2 identical A chains (A2). The A ...nly after the Ca2+ (Kd=10-3M) and fibrin(ogen) (Kd=10-8M) dependent dissociation of the B subunit dimer from the A2' dimer.In the coagulation cascade, factor XIIIa functions to stabilize the fibrin clot by crosslinking the a and g-chains of fibrin. Other proteins known to be substrates for Factor XIIIa which may be hemostatically important include fibronectin, α2-antiplasmin, collagen, factor V, von Willebrand Factor and thrombospondin.Factor XIII is purified from fresh frozen human plasma by a modification of the procedures described by Folke and Lorand involving barium citrate, ammonium sulfate and glycine precipitations, ion exchange chromatography and gel filtration. Factor
Iron(iII)citrate
Ferric ammoniumcitrate is a yellowish brown to red solid with a faint odor of ammonia. It is soluble in water. The primary hazard is the threat to the environment. Immediate steps should be taken to limit its spread to the environment. It is used in medicine, in making blueprints, and as a feed additive. Group: Electrolytes. Alternative Names: IRON (III) CITRATE, GREEN; IRON CITRATE; FERRIC CITRATE; Ferric citrate cell culture tested; Iron(?) citrate; FERRIC CITRATE, TECHNICAL GRADE; CitricAcid,FerricSalt; Iron(III)citrate,Fecontent24-26%. CAS No. 3522-50-7. Product ID: 2-hydroxypropane-1,2,3-tricarboxylate; iron(3+). Molecular formula: 244.94g/mol. Mole weight: C6H5FeO7. C (C (=O)[O-])C (CC (=O)[O-]) (C (=O)[O-])O. [Fe+3]. InChI=1S/C6H8O7.Fe/c7-3(8)1-6(13, 5(11)12)2-4(9)10;/h13H, 1-2H2, (H, 7, 8)(H, 9, 10)(H, 11, 12);/q;+3/p-3. NPFOYSMITVOQOS-UHFFFAOYSA-K.
Iron(iII)citrate
Ferric ammoniumcitrate is a yellowish brown to red solid with a faint odor of ammonia. It is soluble in water. The primary hazard is the threat to the environment. Immediate steps should be taken to limit its spread to the environment. It is used in medicine, in making blueprints, and as a feed additive. Group: Metal & ceramic materials. Alternative Names: IRON (III) CITRATE, GREEN;IRON CITRATE;FERRIC CITRATE;Ferric citrate cell culture tested;Iron(?) citrate;FERRIC CITRATE, TECHNICAL GRADE;CitricAcid, FerricSalt;Iron(III)citrate, Fecontent24-26%. CAS No. 3522-50-7. Molecular formula: C6H5FeO7. Mole weight: 244.94g/mol. IUPACName: 2-hydroxypropane-1,2,3-tricarboxylate;iron(3+). Canonical SMILES: C (C (=O)[O-])C (CC (=O)[O-]) (C (=O)[O-])O. [Fe+3]. Density: 1.8 at 68 °F (USCG, 1999);Specific gravity: 1.8 at 20 °C/4 °C (solid). ECNumber: 214-686-6; 222-536-6; 249-117-0; 219-045-4. Catalog: ACM3522507.
Native Bovine α-L-Fucosidase
In enzymology, an alpha-L-fucosidase (EC 3.2.1.51) is an enzyme that catalyzes the chemical reaction:an alpha-L-fucoside + H2O<-> L-fucose + an alcohol. Thus, the two substrates of this enzyme are alpha-L-fucoside and H2O, whereas its two products are L-fucose and alcohol. This enzyme belongs to the family of hydrolases, specifically those glycosidases that hydrolyse O-and S-glycosyl compounds. This enzyme participates in n-glycan degradation and glycan structures-degradation. Group: Enzymes. Synonyms: α-L-Fucosidase; EC 3.2.1.51; α-fucosidase. Enzyme Commission Number: EC 3.2.1.51. CAS No. 9037-65-4. FUCA. Activity: > 2.0 units/mg protein (biuret). Storage: 2-8°C. Form: ammonium sulfate suspension. Suspension in 3.2 M (NH4)2SO4, 10 mM NaH2PO4 10 mM Citrate, pH 6.0. Source: Bovine kidney. Species: Bovine. α-L-Fucosidase; EC 3.2.1.51; α-fucosidase. Cat No: NATE-0266.
Native Bovine L-Glutamic Dehydrogenase
L-glutamic dehydrogenase catalyzes the conversion of glutamate to α-ketoglutarate. Mammalian forms of this enzyme, including this bovine form, can use either NADP (H) or NAD (H) as coenzymes. L-glutamic dehydrogenase plays a unique role in mammalian metabolism. The reverse reaction catalyzed by this enzyme is the only pathway by which ammonia can become bound to the α-carbon atom of an α-carboxylic acid and thus, is the only source of de novo amino acid synthesis in mammalian species. Group: Enzymes. Synonyms: glutamic dehydrogenase; glutamate dehydrogenase [NAD (P)]; 9029-12-3; glutamate dehydrogenase [NAD (P)+]; EC 1.4.1.3; L-GLDH; L-Glutamate:NAD[P]+ Oxidoreductase (deaminating). Enzyme Commission Number: EC 1.4.1.3. CAS No. 9029-12-3. GLDH. Activity: Type I, > 40 units/mg protein; Type II, > 20 units/mg protein; Type III, > 35 units/mg protein. Storage: 2-8°C. Form: Type I, ammonium sulfate suspension, Suspension in 2.0 M (NH4)2SO4 solution; Type II, lyophilized powder, Contains primarily Citrate buffer salt; Type III, aqueous glycerol solution, Solution in 50% glycerol, pH 7.3. Source: Bovine liver. Species: Bovine. glutamic dehydrogenase; glutamate dehydrogenase [NAD (P)]; 9029-12-3; glutamate dehydrogenase [NAD (P)+]; EC 1.4.1.3; L-GLDH; L-Glutamate:NAD[P]+ Oxidoreductase (deaminating). Cat No: NATE-0392.
Native Pigeon Citrate Synthase
Citrate synthase catalyses the conversion of Citrate to acetyl-CoA in the presence of coenzyme-A with the release of H2O and oxaloacetate. The enzyme has a molecular weight of 85 kDa and a pI of 6.1-6.6. It is inhibited by fluoroacetyl-CoA, palmitoyl-CoA, and citroyl-CoA. It is also inhibited when it is acetylated by acetic anhydride or iodinated by iodine. Group: Enzymes. Synonyms: CS; EC 4.1.3.7; EC 2.3.3.1; 9027-96-7; Citrate (Si)-synthase; (R)-citric synthase; Citrate oxaloacetate-lyase [(pro-3S)-CH2COO-->acetyl-CoA]. Enzyme Commission Number: EC 4.1.3.7. CAS No. 9027-96-7. CS. Activity: 80-150 units/mg protein (modified Warburg-Christian). Storage: 2-8°C. Form: ammonium sulfate suspension. Crystalline suspension in 2.2 M (NH4)2SO4 solution, pH 7.0, containing 6 mM phosphate and 0.5 mM Citrate. Source: Pigeon breast muscle. Species: Pigeon. CS; EC 4.1.3.7; EC 2.3.3.1; 9027-96-7; Citrate (Si)-synthase; (R)-citric synthase; Citrate oxaloacetate-lyase [(pro-3S)-CH2COO-->acetyl-CoA]. Cat No: NATE-0165.
Native Porcine Citrate Synthase
Citrate synthase catalyses the conversion of Citrate to acetyl-CoA in the presence of coenzyme-A with the release of H2O and oxaloacetate. The enzyme has a molecular weight of 85 kDa and a pI of 6.1-6.6. It is inhibited by fluoroacetyl-CoA, palmitoyl-CoA, and citroyl-CoA. It is also inhibited when it is acetylated by acetic anhydride or iodinated by iodine. Group: Enzymes. Synonyms: CS; EC 4.1.3.7; EC 2.3.3.1; 9027-96-7; Citrate (Si)-synthase; (R)-citric synthase; Citrate oxaloacetate-lyase [(pro-3S)-CH2COO-->acetyl-CoA]. Enzyme Commission Number: EC 4.1.3.7. CAS No. 9027-96-7. CS. Activity: > 100 units/mg protein. Storage: 2-8°C. Form: ammonium sulfate suspension. Suspension in 3.2 M (NH4)2SO4 solution, pH 7.0. Source: Porcine heart. Species: Porcine. CS; EC 4.1.3.7; EC 2.3.3.1; 9027-96-7; Citrate (Si)-synthase; (R)-citric synthase; Citrate oxaloacetate-lyase [(pro-3S)-CH2COO-->acetyl-CoA]. Cat No: NATE-0166.
Native Rabbit Aldolase
Fructose-bisphosphate aldolase (EC 4.1.2.13), often just aldolase, is an enzyme catalyzing a reversible reaction that splits the aldol, fructose 1,6-bisphosphate, into the triose phosphates dihydroxyacetone phosphate (DHAP) and glyceraldehyde 3-phosphate (G3P). Aldolase can also produce DHAP from other (3S,4R)-ketose 1-phosphates such as fructose 1-phosphate and sedoheptulose 1,7-bisphosphate. Gluconeogenesis and the Calvin cycle, which are anabolic pathways, use the reverse reaction. Glycolysis, a catabolic pathway, uses the forward reaction. Aldolase is divided into two classes by mechanism. Applications: Aldolase is used to convert fructose 1,6-diphosphate to dihydroxyacetone p...aldolase; fructose diphosphate aldolase; D-fructose-1,6-bisphosphate D-glyceraldehyde-3-phosphate-lyase; EC 4.1.2.13; 9024-52-6. Enzyme Commission Number: EC 4.1.2.13. CAS No. 9024-52-6. Aldolase. Activity: Type I, lyophilized powder, > 8.0 units/mg protein; Type II, ammonium sulfate suspension, 10-20 units/mg protein. Storage: -20°C. Form: lyophilized powder. Essentially sulfate-free containing Citrate buffer salts. Source: Rabbit muscle. Species: Rabbit. aldolase; fructose-1,6-bisphosphate triosephosphate-lyase; Fructose-bisphosphate aldolase; fructose diphosphate aldolase; D-fructose-1,6-bisphosphate D-glyceraldehyde-3-phosphate-lyase; EC 4.1.2.13; 9024-52-6. Cat No: NATE-0048.
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