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| Product | Description | |
|---|---|---|
| Saline Ionic Diluent Buffer | Saline Ionic Diluent Buffer. Group: Molecular Biology. Grades: Purified. US Biological Life Sciences. |  Worldwide |
| Sodium Chloride, 0.85% Aqueous, Normal Saline, Laboratory Grade, 500 mL | Formula: NaCl. F. W: 58. 45. Characteristic: White. Notes: Green chemistry substitute for sodium nitrate. Storage Code: Green; general chemical storage. Group: chem-category greener chemicals. Alternative Names: Table salt. Grades: chem-grade laboratory. CAS No. 7647-14-5. Product ID: 888933. -- SOLD FOR EDUCATIONAL USE ONLY -- |  |
| Tris Buffered Saline Buffer Casein Block, 10X | Tris Buffered Saline (TBS)/Casein Block and Diluent: Group: Biochemicals. Grades: Purified. Pack Sizes: 100ml, 500ml, 1L. US Biological Life Sciences. | Worldwide |
| α amylase | α-Amylase isolated from porcine pancreas is a glycoprotein.2 It is a single polypeptide chain of approximately 475 residues containing 2 SH groups and four disulfide bridges and a tightly bound Ca2+ necessary for stability.3,4 Chloride ions are necessary for activity and stability5 The pH range for activity is 5.5 to 8.0, with the pH optimum at 7.6. Α-amylase from porcine pancreas. Applications: Α-amylase is used to hydrolyze α bonds of α-linked polysaccharides, such as starch and glycogen. product is from porcine pancreas and is type i-a. α-amylase has been used in various plant studies, such as metabolism studies in arabidopsis. Group: Enzymes. S...mission Number: EC 3.2.1.1. CAS No. 9000-90-2. α-Amylase. Mole weight: 51-54 kDa. Activity: 700-1400 units/mg protein (E1%/280). Stability: α-Amylase is stable in 25 mM Tris-HCl, pH 7.5, with 100 mM KCl, at 0 °C or at -20 °C for at least 9 days.8 Another recommended storage condition is in 1 mM phosphate, pH 7.3, with 30 mM CaCl2 at -15 °C. Appearance: Appearance (Color): White to Light Yellow Appearance (Form): Suspension. Form: PMSF treated, saline suspension. Alpha amylase enzyme; for flour; fungal alpha amylase enzyme; enhance quality of flour enzyme; enhance quality; alpha amylase enzyme; flour; alpha amylase; Alpha amylase enzyme for flour; FLO-1301. Cat No: BAK-250. |  |
| Ammonium bromide | FR-11, NH4Br, is the ammonium salt of hydrobromic acid. The chemical crystallizes in colorless prisms, possessing a saline taste; it sublimes on heating and is easily soluble in water. On exposure to air it gradually assumes a yellow color because of the oxidation of traces of bromide (Br-) to bromine (Br2). Group: Electrolytes. Alternative Names: Hydrobromic acid monoammoniate. CAS No. 12124-97-9. Product ID: Azanium; bromide. Molecular formula: 97.94. Mole weight: BrH4N. [NH4+].[Br-]. InChI=1S/BrH.H3N/h1H;1H3. SWLVFNYSXGMGBS-UHFFFAOYSA-N. 99%+. |  |
| Ammonium bromide | FR-11, NH4Br, is the ammonium salt of hydrobromic acid. The chemical crystallizes in colorless prisms, possessing a saline taste; it sublimes on heating and is easily soluble in water. On exposure to air it gradually assumes a yellow color because of the oxidation of traces of bromide (Br-) to bromine (Br2). Group: Metal & ceramic materials. Alternative Names: Hydrobromic acid monoammoniate. CAS No. 12124-97-9. Molecular formula: BrH4N. Mole weight: 97.94. Appearance: White solid. Purity: 99%+. IUPACName: Azanium;bromide. Canonical SMILES: [NH4+].[Br-]. Density: 2.43 g/mL at 25 °C (lit.). ECNumber: 235-183-8. Catalog: ACM12124979. |  |
| Glutathione S-Transferase from E.coli, Recombinant | Glutathione S-transferases (GSTs), previously known as ligandins, comprise a family of eukaryotic and prokaryotic phase II metabolic isozymes best known for their ability to catalyze the conjugation of the reduced form of glutathione (GSH) to xenobiotic substrates for the purpose of detoxification. The GST family consists of three superfamilies:the cytosolic, mitochondrial, and microsomal--also known as MAPEG--proteins. Members of the GST superfamily are extremely diverse in amino acid sequence, and a large fraction of the sequences deposited in public databases are of unknown function. The Enzyme Function Initiative (EFI) is using GSTs as a model superfamily to iden...ferase. Mole weight: 26kDa. Activity: >20 units/mg. Stability: Store at 4°C if entire vial will be used within 2-4 weeks. Store, frozen at -20°C for longer periods of time. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA).Avoid multiple freeze-thaw cycles. Form: Sterile Filtered clear solution in Phosphate Buffered Saline pH 7.4. Source: E.coli. Species: E.coli. Glutathione S-transferases; GSTs; GST; Glutathione S-alkenetransferase; Glutathione S-alkyltransferase; Glutathione S-aralkyltransferase; Glutathione S-aryltransferase; Glutathione S-epoxidetransferase; RX:Glutathione R-transferase; EC 2.5.1.18; 50812-37-8. Cat No: NATE-1945. | |
| Lactate (sodium) (60% in water) | Lactate (60% in water) (Lactic acid) sodium is the product of glycogenolysis and glycolysis [1]. Lactate sodium (60% in water) is an organic salt that is mainly used as a buffer and pH adjuster for injection solutions. Lactate sodium (60% in water) can be metabolized by the body into sodium bicarbonate, which in turn acts to increase the pH of the blood. Lactate sodium (60% in water) is used to improve metabolic acidosis and hypovolemic states. In terms of pharmaceutical preparations, Lactate sodium (60% in water) is often used in combination with sodium chloride, glucose, etc. to form normal saline or compound liquid intravenous injection [2] [3] [4] [5]. Lactate sodium (60% in water) also has antimicrobial activity, which can be used as a food preservative [6]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lactic acid sodium. CAS No. 72-17-3. Pack Sizes: 100 mg (5.34 M * 167 μL in Water); 250 mg (5.34 M * 418 μL in Water); 500 mg (5.34 M * 835 μL in Water); 1 g (5.34 M * 1.67 mL in Water). Product ID: HY-B2227B. |  |
| Magnesium sulfate | Magnesium sulfate is an inorganic salt (chemical compound) containing magnesium, sulfur and oxygen, with the formula MgSO4.It is often encountered as the heptahydrate sulfate mineral epsomite (MgSO4·7H2O), commonly called Epsom salt, taking its name from a bitter saline spring in Epsom in Surrey, England, where the salt was produced from the springs that arise where the porous chalk of the North Downs meets non-porous London clay. The monohydrate, MgSO4·H2O is found as the mineral kieserite. The overall global annual usage in the mid-1970s of the monohydrate was 2.3 million tons, of which the majority was used in agriculture.Anhydrous magnesium sulfate is used as a drying agent. The anhydrous form is hygroscopic (readily absorbs water from the air) and is therefore difficult to weigh accurately; the hydrate is often preferred when preparing solutions (for example, in medical preparations). Epsom salt has been traditionally used as a component of bath salts. Epsom salt can also be used as a beauty product. Athletes use it to soothe sore muscles, while gardeners use it to improve crops. Group: Electrolytes. Alternative Names: Magnesium sulfate anhydrous. CAS No. 7487-88-9. Product ID: Magnesium; sulfate. Molecular formula: 120.37. Mole weight: MgO4S. [O-]S(=O)(=O)[O-].[Mg+2]. InChI=1S/Mg.H2O4S/c;1-5(2, 3)4/h;(H2, 1, 2, 3, 4)/q+2;/p-2. CSNNHWWHGAXBCP-UHFFFAOYSA-L. 99%+. | |
| Magnesium sulfate | Magnesium sulfate is an inorganic salt (chemical compound) containing magnesium, sulfur and oxygen, with the formula MgSO4.It is often encountered as the heptahydrate sulfate mineral epsomite (MgSO4·7H2O), commonly called Epsom salt, taking its name from a bitter saline spring in Epsom in Surrey, England, where the salt was produced from the springs that arise where the porous chalk of the North Downs meets non-porous London clay. The monohydrate, MgSO4·H2O is found as the mineral kieserite. The overall global annual usage in the mid-1970s of the monohydrate was 2.3 million tons, of which the majority was used in agriculture.Anhydrous magnesium sulfate is used as a drying agent. The anhydrous form is hygroscopic (readily absorbs water from the air) and is therefore difficult to weigh accurately; the hydrate is often preferred when preparing solutions (for example, in medical preparations). Epsom salt has been traditionally used as a component of bath salts. Epsom salt can also be used as a beauty product. Athletes use it to soothe sore muscles, while gardeners use it to improve crops. Group: Metal & ceramic materials. Alternative Names: Magnesium sulfate anhydrous. CAS No. 7487-88-9. Molecular formula: MgO4S. Mole weight: 120.37. Appearance: Slightly gray powder. Purity: 99%+. IUPACName: Magnesium;sulfate. Canonical SMILES: [O-]S(=O)(=O)[O-].[Mg+2]. Density: 1.07 g/mL at 20 °C (lit.). ECNumber: 231-298-2. Catalog: ACM74 | |
| Methyl Ethanesulfonate | Methyl Ethanesulfonate (CAS# 1912-28-3 ) is a useful research chemical. Synonyms: TIMTEC-BB SBB009135; MORPHOLINOETHANE SULFONIC ACID; MES BUFFERED SALINE; 2-(N-MORPHOLINO)ETHANESULPHONIC ACID; 2-MORPHOLINOETHANESULFONIC ACID; 4-MORPHOLINOETHANESULFONIC ACID; Methyl ethane sulfonate; Methyl ethane sulphonate. CAS No. 1912-28-3. Molecular formula: C3H8O3S. Mole weight: 124.17. |  |
| Native Bacillus licheniformis α-Amylase | α-Amylase is a protein enzyme EC 3.2.1.1 that hydrolyses alpha bonds of large, alpha-linked polysaccharides, such as starch and glycogen, yielding glucose and maltose. It is the major form of amylase found in Humans and other mammals. It is also present in seeds containing starch as a food reserve, and is secreted by many fungi. Applications: Α-amylase is used to hydrolyze α bonds of α-linked polysaccharides, such as starch and glycogen. this product is from bacillus licheniformis and is type xii-a. α-amylase, from creative enzymes, has been used in various plant studies, such as metabolism studies in arabidopsis. Group: Enzymes. Synonyms: glycogenase; αamylase, α-amylase; 1,4-α-D-glucan glucanohydrolase; EC 3.2.1.1; 9001-19-8; endoamylase; Taka-amylase A. Enzyme Commission Number: EC 3.2.1.1. CAS No. 9001-19-8. α-Amylase. Activity: Type XII-A, saline solution, > 500 units/mg protein (biuret); Type B, liquid. Source: Bacillus licheniformis. glycogenase; αamylase, α-amylase; 1,4-α-D-glucan glucanohydrolase; EC 3.2.1.1; 9001-19-8; endoamylase; Taka-amylase A. Cat No: NATE-0742. | |
| Native Bovine Thrombin | Thrombin is a serine protease that in humans is encoded by the F2 gene. Prothrombin (coagulation factor II) is proteolytically cleaved to form thrombin in the coagulation cascade, which ultimately results in the reduction of blood loss. Thrombin in turn acts as a serine protease that converts soluble fibrinogen into insoluble strands of fibrin, as well as catalyzing many other coagulation-related reactions. Thrombin is the final coagulation protease in regard to hemostasis, promoting both procoagulant and anticoagulant effects. Applications: Thrombin is used for site specific cleavage of recombinant fusion proteins containing an accessible thrombin recognition site for removal of ...Ia; E thrombin; β-thrombin; γ-thrombin. Enzyme Commission Number: EC 3.4.21.5. CAS No. 9002-4-4. Thrombin. Activity: 600-2,000 NIH units/mg protein (biuret) or > 2,000 NIH units/mg protein (E1%/280 = 19.5); > 125 NIH units/mg protein (biuret). Form: Type I, Lyophilized from saline sodium Citrate buffer, pH 6.5; Type II, buffered aqueous solution, In 0.05 M phosphate buffer, pH 7.0. Source: Bovine plasma. Species: Bovine. thrombin; 9002-04-4; EC 3.4.21.5; fibrinogenase; thrombase; thrombofort; topical; thrombin-C; tropostasin; activated blood-coagulation factor II; blood-coagulation factor IIa; factor IIa; E thrombin; β-thrombin; γ-thrombin. Cat No: NATE-0698. | |
| Native Equine Ferritin | Ferritin is a highly specialized protein whose main function is to store excess iron intracellularly. It is widely distributed throughout the animal and plant kingdoms. In mammalian tissues, ferritin is present in concentrated form in spleen, liver and the intestinal mucosa. Ferritin is not a structurally homogeneous protein since purified preparations, when examined by polyacrylamide gel electrophoresis, show multiple bands. Immunologically, ferritins appear to be species specific but not organ specific. Iron: 30% (bipyridyl method). Group: Others. Purity: Not less than 90% as determined by electrophoresis on 4% polyacrylamide gels. Storage: Store at 4° C; Do not freeze. Form: Saline buffer. Source: Equine Spleen. Species: Equine. Ferritin. Cat No: NATE-1876. | |
| Native Fig tree latex Ficin | Ficin is classified as a thiol protease. It contains a single reactive cysteine at its active site. The amino acid homology of the active site is similar to that of papain. Ficin will cleave proteins at the carboxyl side of Gly, Ser, Thr, Met, Lys, Arg, Tyr, Ala, Asn, and Val. The reported Km for the chromogenic substrate pGlu-Phe-Leu-p-nitroanilide is 0.43 mM. Ficin is inhibited by iodoacetamide, iodoacetic acid, N-ethylmaleimide, mercuric chloride, DFP (diisopropyl fluorophosphate), TLCK (Na-p-Tosyl-lysine chloromethyl ketone), and TPCK (N-Tosyl-L-phenylalanine chloromethyl ketone). Ficin can be used to generate high yielding F (ab')2 fragments from mouse IgG1. Group: Enzymes. Synonyms: ficin; debricin; higueroxyl delabarre; EC 3.4.22.3; 9001-33-6; ficain. Enzyme Commission Number: EC 3.4.22.3. CAS No. 9001-33-6. Ficin. Mole weight: 23.8 kDa. Activity: > 1.0 units/mg protein. Form: saline suspension or lyophilized powder. Source: Fig tree latex. ficin; debricin; higueroxyl delabarre; EC 3.4.22.3; 9001-33-6; ficain. Cat No: NATE-0255. | |
| Native Human Cancer Antigen 125 | Cancer Antigen 125 (CA125) is a surface antigen associated with epithelial ovarian cancer. In serum, CA125 is associated with a high molecular weight glycoprotein. Published studies have indicated that elevated serum CA125 levels can be found in individuals with serious endometroid, clear-cell and undifferentiated ovarian carcinoma. Applications: Diagnostic controls; calibrators & standards; immunoassays; clinical chemistry; testing/assay validation; life science; elisa; blotting; manufacturing; tumor markers. Group: Others. Synonyms: MUCIN 16; muc16; CA-125; Cancer Antigen 125. Purity: > 95% (SDS-PAGE). Stability: 2 years. Storage: Store at -20°C. Form: Liquid in phosphate buffered saline, pH 7.4 with sucrose. Source: Human Ascites Fluid. Species: Human. MUCIN 16; muc16; CA-125; Cancer Antigen 125; MUC16. Cat No: NATE-0952. | |
| Native Human Cancer Antigen 19-9 | Cancer Antigen 19-9 is a tumor marker elevated in blood of patients with carcinoma of the gastro-intestinal tract. Primarily used distinguishing pancreatic cancer from pancreatitis, CA 19-9 is not sufficiently specific for use as a cancer screening test. The specificity for pancreatic cancer increases with increasing levels, high levels showing a specificity of >97% for tumor presence. CA 19-9 can be elevated in many types of gastrointestinal cancer, such as colorectal cancer, esophageal cancer and hepatocellular carcinoma. A group of mucin type glycoprotein Sialosyl Lewis Antigens (SLA), such as CA19-9 and CA19-5, have come to be recognized as circulating cancer associated a...plications: Diagnostic controls; calibrators & standards; immunoassays; testing/assay validation; life science; validation studies; manufacturing; tumor markers. Group: Others. Synonyms: Tumor Marker 19-9; CA 19-9; Cancer Antigen 19-9; carbohydrate antigen 19-9; Sialylated Lewis (a) Antigen. Purity: High Purity - Low Cross Contamination of other cancer antigens (Gel filtration & ion-exchange chromatography). Activity: Typically > 500 kU/mL. Stability: 2 years. Appearance: Clear and Colorless. Storage: Store at -20°C. Form: Liquid in phosphate buffered saline, pH 7.4 with sucrose and 0.05% sodium azide. Source: Human Liver Metastases. Species: Human. Tumor Marker 19-9; CA 19-9 | |
| Native Human Cancer Antigen 72-4 | Elevated CA 72-4 levels in serum and plasma have been reported in various malignant diseases including carcinomas of pancreas, stomach, gallbladder, colon, ovaries, cervix and endometrium. The highest diagnostic sensitivities, according to current studies, are found for carcinomas of the gastrointestinal tract and ovaries. Although some benign diseases such as rheumatic diseases or ovary cysts may also result in elevated levels of CA 72-4, clinical studies demonstrated diagnostic specificity of more than 95% for gastrointestinal and ovarian malignancies. There is a good correlation between CA 72-4 levels and tumor stage and size. CA 72-4 is the marker of choice for the therap...dependent marker for the therapeutic monitoring and follow-up care of ovarian cancer patients, in particular in CA 125 negative patients. Applications: Diagnostic controls; calibrators & standards; immunoassays; clinical chemistry; testing/assay validation; life science; elisa; blotting; manufacturing; tumor markers. Group: Others. Synonyms: CA 72-4; Cancer Antigen 72-4. Purity: > 90% (SDS-PAGE). Activity: > 100 kU/mL. Stability: 2 years. Appearance: Clear and colorless. Storage: Store at -20°C. Form: Liquid in phosphate buffered saline, pH 7.4 with sucrose and 0.05% sodium azide. Source: Human Liver Metastases. Species: Human. CA 72-4; Cancer Antigen 72-4. Cat No: NATE-0953. | |
| Native Porcine α-Amylase | α-Amylase is a protein enzyme EC 3.2.1.1 that hydrolyses alpha bonds of large, alpha-linked polysaccharides, such as starch and glycogen, yielding glucose and maltose. It is the major form of amylase found in Humans and other mammals. It is also present in seeds containing starch as a food reserve, and is secreted by many fungi. Applications: Α-amylase is used to hydrolyze α bonds of α-linked polysaccharides, such as starch and glycogen. this product is from porcine pancreas and is type i-a. α-amylase, from creative enzymes, has been used in various plant studies, such as metabolism studies in arabidopsis. Group: Enzymes. Synonyms: glycogenase; αamylase, α-amylase; 1,4-α-D-glucan glucanohydrolase; EC 3.2.1.1; 9001-19-8; endoamylase; Taka-amylase A. Enzyme Commission Number: EC 3.2.1.1. CAS No. 9001-19-8. α-Amylase. Mole weight: 51-54 kDa. Activity: > 1000 units/mg protein (E1%/280); > 10 units/mg solid; 700-1400 units/mg protein (E1%/280). Storage: 2-8°C. Form: saline suspension. Suspension in 2.9 M NaCl solution containing 3 mM CaCl2. Source: Porcine pancreas. Species: Porcine. glycogenase; αamylase, α-amylase; 1,4-α-D-glucan glucanohydrolase; EC 3.2.1.1; 9001-19-8; endoamylase; Taka-amylase A. Cat No: NATE-0745. | |
| Native Rabbit Thrombin | Thrombin is a serine protease that in humans is encoded by the F2 gene. Prothrombin (coagulation factor II) is proteolytically cleaved to form thrombin in the coagulation cascade, which ultimately results in the reduction of blood loss. Thrombin in turn acts as a serine protease that converts soluble fibrinogen into insoluble strands of fibrin, as well as catalyzing many other coagulation-related reactions. The nih assay procedure uses 0.2 ml diluted plasma (1:1 with saline) as a substrate and 0.1 ml of thrombin sample (stabilized in a 1% buffered albumin solution) based on a modification of the method of biggs. only clotting times in the range of 15-25 seconds are used for determining thrombin concentrations. activity is expressed in nih units obtained by direct comparison to a nih thrombin reference standard. Group: Enzymes. Synonyms: thrombin; 9002-04-4; EC 3.4.21. Enzyme Commission Number: EC 3.4.21.5. CAS No. 9002-4-4. Thrombin. Activity: 600-2,000 NIH units/mg protein (biuret) or > 2,000 NIH units/mg protein (E1%/280 = 19.5); > 125 NIH units/mg protein (biuret). Source: Rabbit plasma. Species: Rabbit. thrombin; 9002-04-4; EC 3.4.21.5; fibrinogenase; thrombase; thrombofort; topical; thrombin-C; tropostasin; activated blood-coagulation factor II; blood-coagulation factor IIa; factor IIa; E thrombin; β-thrombin; γ-thrombin. Cat No: NATE-0700. | |
| Native Rat Angiotensin Converting Enzyme | Angiotensin-converting enzyme (EC 3.4.15.1), or "ACE" indirectly increases blood pressure by causing blood vessels to constrict. It does that by converting angiotensin I to angiotensin II, which constricts the vessels. For this reason, drugs known as ACE inhibitors are used to lower blood pressure. ACE, angiotensin I and angiotensin II are part of the renin-angiotensin system (RAS), which controls blood pressure by regulating the volume of fluids in the body. ACE is secreted in the lungs and kidneys by cells in the endothelium (inner layer) of blood vessels. Applications: Positive control. Group: Enzymes. Synonyms: ACE; Angiotensin Converting Enzyme; EC 3.4.15.1; dipeptid....1 M phosphate buffer and 300 mM NaCl at pH 8.3 at 37°C. Storage: Maintain at -20°C in undiluted aliquots for up to 6 months. Avoid repeated freeze/thaw cycles. Form: Liquid in 100 mM phosphate buffered saline, 150 mM NaCl, pH 7.4 with 0.2mM CHAPS. Source: Rat lung. Species: Rat. ACE; Angiotensin Converting Enzyme; EC 3.4.15.1; dipeptidyl carboxypeptidase I; peptidase P; dipeptide hydrolase, peptidyl dipeptidase; angiotensin converting enzyme; kininase II; angiotensin I-converting enzyme; carboxycathepsin; dipeptidyl carboxypeptidase; "hypertensin converting enzyme" peptidyl dipeptidase I; peptidyl-dipeptide hydrolase; peptidyldipeptide hydrolase; endothelial cell peptidy | |
| Parecoxib Impurity 1 | An impurity of Parecoxib. The prodrug Parecoxib as well as its active metabolite val have a specific affinity to the cannabinoid (CB) receptor measured in CB1-expressing HEK 293 cells and rat brain tissue. Adult male Sprague-Dawley rats were administered parecoxib (10 or 30 mg kg(-1), IP) or isotonic saline twice a day starting 24 h after middle cerebral artery occlusion (MCAO) for three consecutive days. The selective COX-2 inhibitor parecoxib was delivered 20 min before or 20 min after the incision by intraperitoneal injection. Pretreatment with parecoxib markedly attenuated the pain hypersensitivity induced by incision. Synonyms: Valdecoxib Disulfonamide Impurity; Parecoxib Impurity H. Grades: 95%. CAS No. 1708094-99-8. Molecular formula: C22H23N3O7S2. Mole weight: 505.56. | |
| Parecoxib Impurity 24 | An impurity of Parecoxib. The prodrug Parecoxib as well as its active metabolite val have a specific affinity to the cannabinoid (CB) receptor measured in CB1-expressing HEK 293 cells and rat brain tissue. Adult male Sprague-Dawley rats were administered parecoxib (10 or 30 mg kg(-1), IP) or isotonic saline twice a day starting 24 h after middle cerebral artery occlusion (MCAO) for three consecutive days. The selective COX-2 inhibitor parecoxib was delivered 20 min before or 20 min after the incision by intraperitoneal injection. Pretreatment with parecoxib markedly attenuated the pain hypersensitivity induced by incision. Synonyms: N-((4-(5-Methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)isobutyramide; 2-methyl-N-[4-(5-methyl-3-phenyl-1,2-oxazol-4-yl)phenyl]sulfonylpropanamide; Propanamide, 2-methyl-N-[[4-(5-methyl-3-phenyl-4-isoxazolyl)phenyl]sulfonyl]-; SCHEMBL5069872; DTXSID50627261; AS-80624; CS-0255351; F83303; 2-Methyl-N-[[4- (5-methyl-3-phenyl-4-isoxazolyl) phenyl]sulfonyl]propanamide; 2-Methyl-N-[4-(5-methyl-3-phenyl-1,2-oxazol-4-yl)benzene-1-sulfonyl]propanamide; 2-METHYL-N-[4-(5-METHYL-3-PHENYL-1,2-OXAZOL-4-YL)BENZENESULFONYL]PROPANAMIDE; N-((4-(5-Methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)isobutyramide (Palbociclib Impurity). Grades: 95%. CAS No. 198470-82-5. Molecular formula: C20H20N2O4S. Mole weight: 384.45. | |
| Potassium bromide crystal optic disc, 13mm x 2mm, polished both sides | Potassium bromide appears as odorless colorless crystals or white crystalline powder or white granular solid with a pungent bitter saline taste. Aqueous solutions are neutral (pH about 7). (NTP, 1992);DryPowder; OtherSolid; PelletsLargeCrystals. Group: Windows & spheres. Product ID: potassium; bromide. Molecular formula: 119g/mol. Mole weight: KBr;BrK. [K+].[Br-]. InChI=1S/BrH.K/h1H;/q;+1/p-1. IOLCXVTUBQKXJR-UHFFFAOYSA-M. | |
| Potassium bromide crystal optic rectangle, 30mm x 15mm x 4mm, unpolished | Potassium bromide appears as odorless colorless crystals or white crystalline powder or white granular solid with a pungent bitter saline taste. Aqueous solutions are neutral (pH about 7). (NTP, 1992);DryPowder; OtherSolid; PelletsLargeCrystals. Group: Windows & spheres. Product ID: potassium; bromide. Molecular formula: 119g/mol. Mole weight: KBr;BrK. [K+].[Br-]. InChI=1S/BrH.K/h1H;/q;+1/p-1. IOLCXVTUBQKXJR-UHFFFAOYSA-M. | |
| Potassium bromide crystal optic rectangle, 38.5mm x 19.5mm x 4mm (drilled), polished both sides | Potassium bromide appears as odorless colorless crystals or white crystalline powder or white granular solid with a pungent bitter saline taste. Aqueous solutions are neutral (pH about 7). (NTP, 1992);DryPowder; OtherSolid; PelletsLargeCrystals. Group: Windows & spheres. Product ID: potassium; bromide. Molecular formula: 119g/mol. Mole weight: KBr;BrK. [K+].[Br-]. InChI=1S/BrH.K/h1H;/q;+1/p-1. IOLCXVTUBQKXJR-UHFFFAOYSA-M. | |
| Potassium chloride crystal optic disc, 13mm x 1mm, polished both sides | Potassium chloride appears as white colorless cubic crystals. Strong saline taste. (NTP, 1992);DryPowder; DryPowder, Liquid; Liquid; OtherSolid; OtherSolid, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, Liquid;Colourless, elongated, prismatic or cubital crystals or white granular powder. Odourless;COLOURLESS HYGROSCOPIC CRYSTALS. Group: Windows & spheres. Product ID: potassium; chloride. Molecular formula: 74.55g/mol. Mole weight: KCl;KCl;KCl;ClK. [Cl-].[K+]. InChI=1S/ClH.K/h1H;/q;+1/p-1. WCUXLLCKKVVCTQ-UHFFFAOYSA-M. | |
| Potassium chloride crystal optic disc, 13mm x 2mm, unpolished | Potassium chloride appears as white colorless cubic crystals. Strong saline taste. (NTP, 1992);DryPowder; DryPowder, Liquid; Liquid; OtherSolid; OtherSolid, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, Liquid;Colourless, elongated, prismatic or cubital crystals or white granular powder. Odourless;COLOURLESS HYGROSCOPIC CRYSTALS. Group: Windows & spheres. Product ID: potassium; chloride. Molecular formula: 74.55g/mol. Mole weight: KCl;KCl;KCl;ClK. [Cl-].[K+]. InChI=1S/ClH.K/h1H;/q;+1/p-1. WCUXLLCKKVVCTQ-UHFFFAOYSA-M. | |
| Potassium chloride crystal optic disc, 25mm x 2mm, polished both sides | Potassium chloride appears as white colorless cubic crystals. Strong saline taste. (NTP, 1992);DryPowder; DryPowder, Liquid; Liquid; OtherSolid; OtherSolid, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, Liquid;Colourless, elongated, prismatic or cubital crystals or white granular powder. Odourless;COLOURLESS HYGROSCOPIC CRYSTALS. Group: Windows & spheres. Product ID: potassium; chloride. Molecular formula: 74.55g/mol. Mole weight: KCl;KCl;KCl;ClK. [Cl-].[K+]. InChI=1S/ClH.K/h1H;/q;+1/p-1. WCUXLLCKKVVCTQ-UHFFFAOYSA-M. | |
| Potassium chloride crystal optic disc, 32mm x 3mm (drilled), polished both sides | Potassium chloride appears as white colorless cubic crystals. Strong saline taste. (NTP, 1992);DryPowder; DryPowder, Liquid; Liquid; OtherSolid; OtherSolid, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, Liquid;Colourless, elongated, prismatic or cubital crystals or white granular powder. Odourless;COLOURLESS HYGROSCOPIC CRYSTALS. Group: Windows & spheres. Product ID: potassium; chloride. Molecular formula: 74.55g/mol. Mole weight: KCl;KCl;KCl;ClK. [Cl-].[K+]. InChI=1S/ClH.K/h1H;/q;+1/p-1. WCUXLLCKKVVCTQ-UHFFFAOYSA-M. | |
| Potassium chloride crystal optic disc, 32mm x 3mm, polished both sides | Potassium chloride appears as white colorless cubic crystals. Strong saline taste. (NTP, 1992);DryPowder; DryPowder, Liquid; Liquid; OtherSolid; OtherSolid, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, Liquid;Colourless, elongated, prismatic or cubital crystals or white granular powder. Odourless;COLOURLESS HYGROSCOPIC CRYSTALS. Group: Windows & spheres. Product ID: potassium; chloride. Molecular formula: 74.55g/mol. Mole weight: KCl;KCl;KCl;ClK. [Cl-].[K+]. InChI=1S/ClH.K/h1H;/q;+1/p-1. WCUXLLCKKVVCTQ-UHFFFAOYSA-M. | |
| Potassium chloride crystal optic disc, 32mm x 3mm, unpolished | Potassium chloride appears as white colorless cubic crystals. Strong saline taste. (NTP, 1992);DryPowder; DryPowder, Liquid; Liquid; OtherSolid; OtherSolid, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, Liquid;Colourless, elongated, prismatic or cubital crystals or white granular powder. Odourless;COLOURLESS HYGROSCOPIC CRYSTALS. Group: Windows & spheres. Product ID: potassium; chloride. Molecular formula: 74.55g/mol. Mole weight: KCl;KCl;KCl;ClK. [Cl-].[K+]. InChI=1S/ClH.K/h1H;/q;+1/p-1. WCUXLLCKKVVCTQ-UHFFFAOYSA-M. | |
| Potassium chloride crystal optic disc, 38mm x 6mm, polished both sides | Potassium chloride appears as white colorless cubic crystals. Strong saline taste. (NTP, 1992);DryPowder; DryPowder, Liquid; Liquid; OtherSolid; OtherSolid, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, Liquid;Colourless, elongated, prismatic or cubital crystals or white granular powder. Odourless;COLOURLESS HYGROSCOPIC CRYSTALS. Group: Windows & spheres. Product ID: potassium; chloride. Molecular formula: 74.55g/mol. Mole weight: KCl;KCl;KCl;ClK. [Cl-].[K+]. InChI=1S/ClH.K/h1H;/q;+1/p-1. WCUXLLCKKVVCTQ-UHFFFAOYSA-M. | |
| Potassium chloride crystal optic rectangle, 30mm x 15mm x 4mm, (drilled), polished both sides | Potassium chloride appears as white colorless cubic crystals. Strong saline taste. (NTP, 1992);DryPowder; DryPowder, Liquid; Liquid; OtherSolid; OtherSolid, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, Liquid;Colourless, elongated, prismatic or cubital crystals or white granular powder. Odourless;COLOURLESS HYGROSCOPIC CRYSTALS. Group: Windows & spheres. Product ID: potassium; chloride. Molecular formula: 74.55g/mol. Mole weight: KCl;KCl;KCl;ClK. [Cl-].[K+]. InChI=1S/ClH.K/h1H;/q;+1/p-1. WCUXLLCKKVVCTQ-UHFFFAOYSA-M. | |
| Potassium chloride crystal optic rectangle, 30mm x 15mm x 4mm, polished both sides | Potassium chloride appears as white colorless cubic crystals. Strong saline taste. (NTP, 1992);DryPowder; DryPowder, Liquid; Liquid; OtherSolid; OtherSolid, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, Liquid;Colourless, elongated, prismatic or cubital crystals or white granular powder. Odourless;COLOURLESS HYGROSCOPIC CRYSTALS. Group: Windows & spheres. Product ID: potassium; chloride. Molecular formula: 74.55g/mol. Mole weight: KCl;KCl;KCl;ClK. [Cl-].[K+]. InChI=1S/ClH.K/h1H;/q;+1/p-1. WCUXLLCKKVVCTQ-UHFFFAOYSA-M. | |
| Potassium chloride crystal optic rectangle, 38.5mm x 19.5mm x 4mm, unpolished | Potassium chloride appears as white colorless cubic crystals. Strong saline taste. (NTP, 1992);DryPowder; DryPowder, Liquid; Liquid; OtherSolid; OtherSolid, Liquid; PelletsLargeCrystals; PelletsLargeCrystals, Liquid;Colourless, elongated, prismatic or cubital crystals or white granular powder. Odourless;COLOURLESS HYGROSCOPIC CRYSTALS. Group: Windows & spheres. Product ID: potassium; chloride. Molecular formula: 74.55g/mol. Mole weight: KCl;KCl;KCl;ClK. [Cl-].[K+]. InChI=1S/ClH.K/h1H;/q;+1/p-1. WCUXLLCKKVVCTQ-UHFFFAOYSA-M. | |
| Potassium fluoride | Potassium fluoride appears as white powder or crystals with a sharp saline taste. Shipped as a solid or an aqueous solution. Strongly irritates skin, eyes and mucous membranes. Toxic by ingestion. Used in insecticides, solder flux and etching glass.;DryPowder; DryPowder, Liquid; Liquid; PelletsLargeCrystals. Group: Kf. Product ID: potassium; fluoride. Molecular formula: 58.097g/mol. Mole weight: FK. InChI=1S/FH.K/h1H;/q;+1/p-1. NROKBHXJSPEDAR-UHFFFAOYSA-M. 0.9999. | |
| Potassium fluoride on alumina | Potassium fluoride appears as white powder or crystals with a sharp saline taste. Shipped as a solid or an aqueous solution. Strongly irritates skin, eyes and mucous membranes. Toxic by ingestion. Used in insecticides, solder flux and etching glass.;DryPowder; DryPowder, Liquid; Liquid; PelletsLargeCrystals. Group: Electrolytes. Product ID: potassium; fluoride. Molecular formula: 58.097g/mol. Mole weight: KF;FK. [F-].[K+]. InChI=1S/FH.K/h1H;/q;+1/p-1. NROKBHXJSPEDAR-UHFFFAOYSA-M. | |
| Reactive blue 2 | Reactive blue 2. Alternative Names: BASILEN BLUE E-3G;CI NO 61211;CI 61211;CIBACRON BLUE F3GA;CIBACRON BLUE 3G-A;1-AMINO-4-[[4-[[4-CHLORO-6-[[3 (OR 4)-SULFOPHENYL]AMINO]-1,3,5-TRIAZIN-2-YL]AMINO]-3-SULFOPHENYL]AMINO]-9,10-DIHYDRO-9,10-DIOXO-2-ANTHRACENESULFONIC ACID;REACTIVE BLUE 2;PROCION BLUE HB. CAS No. 12236-82-7. Molecular formula: C29H20ClN7O11S3. Mole weight: 774.16. Appearance: saline suspension. Purity: 0.96. IUPACName: 1-amino-4-[4-[[4-chloro-6-(3-sulfoanilino)-1,3,5-triazin-2-yl]amino]-3-sulfoanilino]-9,10-dioxoanthracene-2-sulfonicacid. Canonical SMILES: C1=CC=C2C (=C1)C (=O)C3=C (C2=O)C (=C (C=C3NC4=CC (=C (C=C4)NC5=NC (=NC (=N5)NC6=CC (=CC=C6)S (=O) (=O)O)Cl)S (=O) (=O)O)S (=O) (=O)O)N. Density: 1.845 g/cm³. ECNumber: 235-465-0. Catalog: ACM12236827. | |
| Sodium 2-Hydroxypropiomate Solution | Sodium lactate occurs as a clear, colorless, slightly syrupy liquid. It is odorless, or has a slight odor with a characteristic saline taste. It is hygroscopic. Synonyms: E325; 2-hydroxypropanoic acid monosodium salt; Lacolin; lactic. acid monosodium salt; lactic acid sodium salt; natrii lactatis solutio. Patlac; Purasal; Ritalac NAL; sodium a-hydroxypropionate. CAS No. 72-17-3. Product ID: PE0407. Molecular formula: C3H5NaO3. Mole weight: 112.06. Category: Humectants; Stabilizers; pH adjuster; Wetting agents. Product Keywords: Pharmaceutical Excipients; Other Materials; Humectants; Sodium 2-Hydroxypropiomate Solution; PE0407; TU7HW0W0QT; 72-17-3; 72-17-3. UNII: TU7HW0W0QT. Chemical Name: Sodium lactate. Grade: Pharmceutical Excipients. Administration route: Infiltration; Intraperitoneal; Intravenous; Oral; Intracardiac; Intramuscular; Subcutaneous. Dosage Form: Epidural, IM, IV, and SC injections; oral. suspensions; topical gels and solutions. Stability and Storage Conditions: Sodium lactate should be stored in a well-closed container in a cool,dry, place. Sodium lactate is combustible and decomposes upon heating. Commonly used amount and the maximum amount: The maximum dosage for intravenous injection: 50mg; the maximum dosage for general topical preparations: 51.3mg/g. Source and Preparation: Add sodium hydroxide to lactic acid under cooling conditions to carry out neutralization reaction, th |  |
| Sodium Bicarbonate | Sodium bicarbonate occurs as an odorless, white, crystalline powder with a saline, slightly alkaline taste. The crystal structure is monoclinic prisms. Grades with different particle sizes, from a fine powder to free-flowing uniform granules, are commercially available. Synonyms: Baking soda; E500; Effer-Soda; monosodium carbonate; natrii hydrogenocarbonas; Sal de Vichy; sodium acid carbonate; sodium hydrogen carbonate. CAS No. 144-55-8. Product ID: PE-0619. Molecular formula: NaHCO3. Mole weight: 84.01. Category: Alkalizing Agents; therapeutic AgentsAcid-Base regulator; Effervescent Disintegrant; Buffer (in solution); Freeze-drying Stabilizer; Gas forming Agents. Product Keywords: Other Materials; Stabilizers; PE-0619; Sodium Bicarbonate; Alkalizing Agents; therapeutic AgentsAcid-Base regulator; Effervescent Disintegrant; Buffer (in solution); Freeze-drying Stabilizer; Gas forming Agents; NaHCO3; 144-55-8. UNII: 8MDF5V39QO. Chemical Name: Carbonic acid monosodium salt. Grade: Pharmceutical Excipients. Administration route: Injections; ophthalmic; oral. Dosage Form: Injections; ophthalmic preparations; oral capsules, solutions, and tablets. Stability and Storage Conditions: When heated to about 50°C, sodium bicarbonate begins to dissociate into carbon dioxide, sodium carbonate, and water; on heating to 250-300°C, for a short time, sodium bicarbonate is completely converted into anhydrous sodium carbonate. Source a | |
| Sodium Citrate | Sodium citrate dihydrate consists of odorless, colorless, monoclinic crystals, or a white crystalline powder with a cooling, saline taste. It is slightly deliquescent in moist air, and in warm dry air it is efflorescent. Although most pharmacopeias specify that sodium citrate is the dihydrate, the USP states that sodium citrate may be either the dihydrate or anhydrous material. Synonyms: Citric acid trisodium salt; E331; natrii citras; sodium citrate tertiary; trisodium citrate. CAS No. 6132-4-3. Product ID: PE-0124. Molecular formula: C6H5Na3O7·2H2O. Mole weight: 294.1. Category: Alkalizing Agents; Buffering Agents; Emulsifying Agents; Sequestering Agents. Product Keywords: Flavoring Agents; Stabilizers; pH Modifier Excipients; ; PE-0124; Sodium Citrate; Alkalizing Agents; Buffering Agents; Emulsifying Agents; Sequestering Agents; C6H5Na3O7·2H2O; 6132-04-03. UNII: 1Q73Q2JULR. Chemical Name: Trisodium 2-hydroxypropane-1, 2, 3-tricarboxylate dihydrate. Grade: Pharmceutical Excipients. Administration route: Inhalations; injections; ophthalmic; oral; nasal, otic, rectal, topical, transdermal, and vaginal. Dosage Form: Inhalations; injections; ophthalmic products; oral solutions, suspensions, syrups and tablets; nasal, otic, rectal, topical, transdermal, and vaginal preparations. Stability and Storage Conditions: Sodium citrate dihydrate is a stable material. Aqueous solutions may be sterilized by autoclaving. On storag | |
| Sodium Citrate Dihydrate | Sodium citrate dihydrate consists of odorless, colorless, monoclinic crystals, or a white crystalline powder with a cooling, saline taste. It is slightly deliquescent in moist air, and in warm dry air it is efflorescent. Although most pharmacopeias specify that sodium citrate is the dihydrate, the USP states that sodium citrate may be either the dihydrate or anhydrous material. Synonyms: Citric acid trisodium salt; E331; natrii citras; sodium citrate tertiary; trisodium citrate. CAS No. 6132-4-3. Product ID: PE-0542. Molecular formula: C6H5Na3O7·2H2O. Mole weight: 294.1. Category: Alkalizing Agents; Buffering Agents; Emulsifying Agents; Sequestering Agents. Product Keywords: Excipients for Liquid Dosage Form; Emulsifier Excipients; PE-0542; Sodium Citrate Dihydrate; Alkalizing Agents; Buffering Agents; Emulsifying Agents; Sequestering Agents; C6H5Na3O7·2H2O; 6132-04-3. UNII: 1Q73Q2JULR. Chemical Name: Trisodium 2-hydroxypropane-1, 2, 3-tricarboxylate dihydrate. Grade: Pharmceutical Excipients. Administration route: Inhalations; injections; ophthalmic; oral; nasal, otic, rectal, topical, transdermal, and vaginal. Dosage Form: Inhalations; injections; ophthalmic products; oral solutions, suspensions, syrups and tablets; nasal, otic, rectal, topical, transdermal, and vaginal preparations. Stability and Storage Conditions: Sodium citrate dihydrate is a stable material. Aqueous solutions may be sterilized by au | |
| Sodium Lactate | Sodium lactate occurs as a clear, colorless, slightly syrupy liquid. It is odorless, or has a slight odor with a characteristic saline taste. It is hygroscopic. Synonyms: E325; 2-hydroxypropanoic acid monosodium salt; Lacolin; lactic acid monosodium salt; lactic acid sodium salt; natrii lactatis solutio; Patlac; Purasal; Ritalac NAL; sodium a-hydroxypropionate. CAS No. 72-17-3. Product ID: PE-0556. Molecular formula: C3H5NaO3. Mole weight: 112.06. Category: Antimicrobial Preservative; Buffering Agents; Emulsifying Agents; flavoring Agents; Humectant. Product Keywords: Stabilizers; Emulsifier Excipients; PE-0556; Sodium Lactate; Antimicrobial Preservative; Buffering Agents; Emulsifying Agents; flavoring Agents; Humectant; C3H5NaO3; 72-17-3. UNII: TU7HW0W0QT. Chemical Name: Sodium lactate. Grade: Pharmceutical Excipients. Administration route: Infiltration; Intraperitoneal; Intravenous; Oral; Intracardiac; Intramuscular; Subcutaneous. Dosage Form: Epidural, IM, IV, and SC injections; oral suspensions; topical gels and solutions. Stability and Storage Conditions: Sodium lactate should be stored in a well-closed container in a cool, dry, place. Sodium lactate is combustible and decomposes upon heating. Commonly used amount and the maximum amount: The maximum dosage for intravenous injection: 50mg; the maximum dosage for general topical preparations: 51.3mg/g. Source and Preparation: Add sodium hydroxide to lactic acid u | |
| Tetrapotassium hexacyanoferrate trihydrate | Tetrapotassium hexacyanoferrate trihydrate. Synonyms: potassiumhexacyanide; potassiumhexacyanoferrate(iv); tetrapotassium, (oc-6-11)-ferrate(4-hexakis(cyano-c)-; tetrapotassiumferrocyanide; Tetrapotassium hexac;IODINE BROMIDE SOLUTION PHE;hexacyano-ferrate(4-tetrapotassium;hexakis(cyano-C)-,tetrapotassium,(OC-6-11)-Ferrate(4-). CAS No. 13943-58-3. Pack Sizes: 1 kg. Product ID: CDF4-0006. Molecular formula: C24H6Fe4K4N24O3-8. Category: Anticaking Agents. Product Keywords: Food Ingredients; Anticaking Agents; Tetrapotassium hexacyanoferrate trihydrate; CDF4-0006; 13943-58-3; C24H6Fe4K4N24O3-8; 237-722-2; 13943-58-3. Purity: 0.98. Color: Yellow granules (rough estimate). EC Number: 237-722-2. Application: Potassium cyanide and ferricyanide, dry colors, tempering steel, dyeing, explosives, process engrav- ing and lithography, laboratory reagent. Boiling Point: 104.2 °C. Melting Point: 70 °C. Density: 1.85 g/mL. Product Description: Also known as yellow prussiate of potash, K4Fe(CN)6.3H20 is yellow crystals with a saline taste that are soluble in water,insoluble in alcohol and loses water at 60°C. Used in medicine,dry colors,explosives, and as an analytical reagent. | |
| Thymus Extract, Calf | Calf Thymus Extract forms precipitins with autoantibodies that bind Sm, nRNP, La/SS-B, and Jo-1 when tested by immunodiffusion. Calf thymus is extracted in phosphate buffered saline. Insoluble material is removed. Extractable nuclear antigens are lyophilized. Group: Biologicals. Grades: Purified. Pack Sizes: 500ul. US Biological Life Sciences. | Worldwide |
| Tissue, Acetone Powder, Human Brain HisTek | Tissue powders are produced by saline wash of ruptured cells obtained from tissue and multiple precipitations in acetone, removing lipids. Suitable for use as a specific adsorbent to remove unwanted reactivities or as a source material. It is relatively stable, and is used in the preparation of some enzymes. Group: Biologicals. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Tissue, Acetone Powder, Human Liver HisTek | Tissue powders are produced by saline wash of ruptured cells obtained from tissue and multiple precipitations in acetone, removing lipids. Suitable for use as a specific adsorbent to remove unwanted reactivities or as a source material. It is relatively stable, and is used in the preparation of some enzymes. Group: Biologicals. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Tissue, Acetone Powder, Mouse Liver HisTek | Tissue powders are produced by saline wash of ruptured cells obtained from tissue and multiple precipitations in acetone, removing lipids. Group: Biologicals. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Valdecoxib Impurity J | The prodrug Parecoxib as well as its active metabolite val have a specific affinity to the cannabinoid (CB) receptor measured in CB1-expressing HEK 293 cells and rat brain tissue. Adult male Sprague-Dawley rats were administered parecoxib (10 or 30 mg kg(-1), IP) or isotonic saline twice a day starting 24 h after middle cerebral artery occlusion (MCAO) for three consecutive days. The selective COX-2 inhibitor parecoxib was delivered 20 min before or 20 min after the incision by intraperitoneal injection. Pretreatment with parecoxib markedly attenuated the pain hypersensitivity induced by incision. Uses: Cyclooxygenase 2 inhibitors. Synonyms: SC 69124; SC69124; SC-69124; Valus-P; Vorth-P. Grades: >98%. CAS No. 198470-84-7. Molecular formula: C19H18N2O4S. Mole weight: 370.42. | |
| acyl-lipid (11-3)-desaturase | The enzyme, characterized from the protist Euglena gracilis and the microalga Rebecca salina, introduces a cis double bond at the 8-position in 20-carbon fatty acids that are incorporated into a glycerolipid and have an existing Δ11 desaturation. The enzyme is a front-end desaturase, introducing the new double bond between the pre-existing double bond and the carboxyl-end of the fatty acid. It contains a cytochrome b5 domain that acts as the direct electron donor to the active site of the desaturase, and does not require an external cytochrome. Involved in alternative pathways for the biosynthesis of the polyunsaturated fatty acids arachidonate and icosapentaenoate. Group: Enzymes. Synonyms: acyl-lipid 8-desaturase; Δ8 fatty acid desaturase; Δ8-desaturase; Δ8-fatty-acid desaturase; efd1 (gene name); D8Des (gene name); phytosphinganine,hydrogen donor:oxygen Δ. Enzyme Commission Number: EC 1.14.19.4. 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-1004; acyl-lipid (11-3)-desaturase; EC 1.14.19.4; acyl-lipid 8-desaturase; Δ8 fatty acid desaturase; Δ8-desaturase; Δ8-fatty-acid desaturase; efd1 (gene name); D8Des (gene name); phytosphinganine,hydrogen donor:oxygen Δ8-oxidoreductase (incorrect); SLD. Cat No: EXWM-1004. | |
| acyl-lipid (8-3)-desaturase | The enzyme, which has been characterized from multiple organisms including the moss Physcomitrella patens, the marine microalga Rebecca salina, and the filamentous fungus Mortierella alpina, introduces a cis double bond at the 5-position in 20-carbon polyunsaturated fatty acids incorporated in a glycerolipid that contain a Δ8 double bond. The enzyme contains a cytochrome b5 domain that acts as the direct electron donor to the active site of the desaturase, and does not require an external cytochrome. Group: Enzymes. Synonyms: acyl-lipid 5-desaturase; Δ5-fatty-acid desaturase; DES5 (gene name); D5des (gene name); FADS1. Enzyme Commission Number: EC 1.14.19.30. 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-0994; acyl-lipid (8-3)-desaturase; EC 1.14.19.30; acyl-lipid 5-desaturase; Δ5-fatty-acid desaturase; DES5 (gene name); D5des (gene name); FADS1. Cat No: EXWM-0994. | |
| adenosyl-chloride synthase | This enzyme, isolated from the marine bacterium Salinispora tropica, catalyses an early step in the pathway leading to biosynthesis of the proteosome inhibitor salinosporamide A. The enzyme is very similar to EC 2.5.1.63, adenosyl-fluoride synthase, but does not accept fluoride. Group: Enzymes. Synonyms: chlorinase; 5'-chloro-5'-deoxyadenosine synthase. Enzyme Commission Number: EC 2.5.1.94. 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-2833; adenosyl-chloride synthase; EC 2.5.1.94; chlorinase; 5'-chloro-5'-deoxyadenosine synthase. Cat No: EXWM-2833. | |
| Deoxyfusapyrone | It is a broad spectrum antifungal metabolite isolated from several fusarium species. It exhibits low zoo-toxicity as evidenced by a lack of toxicity against artemia salina. It is a useful candidate for control of postharvest crop diseases. Synonyms: Deoxyneofusapyrone; 3-(4-deoxy-β-xylo-hexopyranosyl)-2-hydroxy-6-[(3E,5E,8Z)-2-hydroxy-1,1,5,7,9,11-hexamethyl-3,5,8-heptadecatrien-1-yl]-4H-pyran-4-one. Grades: >98% by HPLC. CAS No. 156856-32-5. Molecular formula: C34H54O8. Mole weight: 590.79. | |
| Desotamide | It is a cyclic hexapeptide antibiotic first isolated from streptomyces sp. It was found to produce Salinamide A, an inhibitor of bacterial RNA polymerase. It has activity against S. aureus, S. pneumoniae and methicillin-resistant S. epidermidis. Synonyms: Cyclo(L-alloisoleucyl-L-asparaginylglycyl-L-tryptophyl-L-leucyl-D-leucyl); cyclo[L-asparagyl-glycyl-L-tryptophyl-L-leucyl-D-leucyl-L-alloisoleucyl]; Desotamide A. Grades: >95% by HPLC. CAS No. 194660-14-5. Molecular formula: C35H52N8O7. Mole weight: 696.84. | |
| Desotamide | The cyclic hexapeptide, desotamide, was first isolated from a Streptomyces sp. found to produce salinamide A, an inhibitor of bacterial RNA polymerase. Little is known of its biological potency or intrinsic activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 194660-14-5. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Dunaliella Salina Micro-Algae Extract | Highly purified extract from the microalgae Dunaliella salina consisting of a powerful blend of active substances including amino acids and carbohydrates. Visibly energizes and rejuvenates skin. Has effective moisturizing and skin-conditioning properties. Uses: Anti-aging, rejuvenating, revitalizing skin care products. Group: Skin actives. CAS No. 7732-18-5 / 9004-78-8 / 532-32-1 / 24634-61-5. Appearance: Pale-yellow liquid. Catalog: CI-SC-1043. | |
| Dunaliella Salina P.E. 7.5% Carotenoids HPLC | Dunaliella Salina P.E. 7.5% Carotenoids HPLC. |  CA, FL & NJ |
| Fusapyrone | It is a broad spectrum antifungal metabolite isolated from several species of fusarium. It exhibits low animal-toxicity as evidenced by a lack of toxicity against artemia salina. It is a useful candidate for control of postharvest crop diseases. Synonyms: 3-(4-deoxy-β-xylo-hexopyranosyl)-2-hydroxy-6-[(3E,5E,8Z)-2-hydroxy-7-(hydroxymethyl)-1,1,5,9,11-pentamethyl-3,5,8-heptadecatrien-1-yl]-2H-pyran-2-one; Neofusapyrone. Grades: >95%. CAS No. 156856-31-4. Molecular formula: C34H54O9. Mole weight: 606.79. | |
| Marizomib | Marizomib (Salinosporamide A) is a second-generation, irreversible, brain-penetrant, pan-proteasome inhibitor. Marizomib inhibits the CT-L (β5), CT-T-laspase-like (C-L, β1) and trypsin-like (T-L, β2) activities of the 20S proteasome (IC 50 =3.5, 28, and 430 nM, respectively) [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Salinosporamide A; NPI-0052. CAS No. 437742-34-2. Pack Sizes: 100 μg; 500 μg; 1 mg; 5 mg. Product ID: HY-10985. | |
| Miyakamide A1 | Miyakamide A1 is an antibiotic produced by Aspergillus flavus var. columnaris FKI-0739. It has insecticidal effect. Miyakamide A1 inhibits the growth of Artemia salina at a minimum concentration of 5 μg/mL. Miyakamide A1 has weak antixanthomonas activity. It inhibits P388 cells with an IC50 of 10.5 μg/mL. CAS No. 497252-38-7. Molecular formula: C31H32N4O3. Mole weight: 508.61. | |
| Miyakamide A2 | Miyakamide A2 is an antibiotic produced by Aspergillus flavus var. columnaris FKI-0739. It has insecticidal effect. Miyakamide A2 inhibits the growth of Artemia salina at a minimum concentration of 5 μg/mL. Miyakamide A1 has weak antixanthomonas activity. It inhibits P388 cells with an IC50 of 12.2 μg/mL. CAS No. 497252-39-8. Molecular formula: C31H32N4O3. Mole weight: 508.61. | |
| Miyakamide B1 | Miyakamide B1 is an antibiotic produced by Aspergillus flavus var. columnaris FKI-0739. It has insecticidal effect. Miyakamide B1 inhibits the growth of Artemia salina at a minimum concentration of 20 μg/mL. It inhibits P388 cells with an IC50 of 8.8 μg/mL. CAS No. 497182-82-8. Molecular formula: C31H32N4O4. Mole weight: 524.61. | |
| Miyakamide B2 | Miyakamide B2 is an antibiotic produced by Aspergillus flavus var. columnaris FKI-0739. It has insecticidal effect. Miyakamide B2 inhibits the growth of Artemia salina at a minimum concentration of 20 μg/mL. It inhibits P388 cells with an IC50 of 7.6 μg/mL. CAS No. 497182-83-9. Molecular formula: C31H32N4O4. Mole weight: 524.61. | |
| Narasin sodium | It is a polyether antibiotic produced by Str. aureo faciens NRRL 5758. It has broad spectrum activity against gram-positive bacteria, anaerobic bacteria and mycoplasma. It also has antiviral and limited antifungal activity. Synonyms: 4-Methylsalinomycin sodium; 1,6,8-Trioxadispiro[4.1.5.3]pentadecane, Salinomycin deriv.; (4S)-4-Methyl Salinomycin Monosodium Salt; Monteban sodium; Narasin A sodium. Grades: >98% by HPLC. CAS No. 58331-17-2. Molecular formula: C43H71NaO11. Mole weight: 787.01. | |
| Polyquaternium 7 | Polyquaternium 7 is a filtration reducer under high temperatures and high salinities. Group: Biochemicals. Grades: Highly Purified. CAS No. 26590-05-6. Pack Sizes: 100mg, 500mg, 1g. Molecular Formula: (C11H21ClN2O)x, Molecular Weight: 232.75. US Biological Life Sciences. | Worldwide |
| Salicylanilide | Salicylanilide has a wide range of biological activities, including antiviral, anti-inflammatory, antibacterial and so on. It inhibits HIV virus by targeting HIV-1 integrase or reverse transcriptase. It inhibits mycobacterial isocitrate lyase (ICL) and has a significant antimycobacterial effect. It can be used as an antiseptic. Synonyms: 2-Hydroxybenzanilide; 2-(N-Phenylcarboxamido)phenol; 2-(Phenylaminocarbonyl)phenol; Ansadol; Aseptolan; Hyanilid; N-Phenyl-2-hydroxybenzamide; N-Phenylsalicylamide; NSC 14881; Salicylanilid; Salicylic acid anilide; Salifebrin; Salinide; Salinidol; Salnide; Shirlan; o-Hydroxybenzanilide. Grades: ≥95%. CAS No. 87-17-2. Molecular formula: C13H11NO2. Mole weight: 213.23. | |
| Salinomycin | 5mg Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C42H70O11. CAS No. 53003-10-4. Prepack ID 10569390-5mg. Molecular Weight 751. See USA prepack pricing. |  |
| Salinomycin | from Streptomyces albus, ≥98% (HPLC). Uses: For analytical and research use. Group: Fluorescence/luminescence spectroscopy; chiral molecules. Alternative Names: 1,6,8-Trioxadispiro[4.1.5.3]pentadecane, salinomycin deriv., Stereoisomer of α-ethyl-6-[5-[2-(5-ethyltetrahydro-5-hydroxy-6-methyl-2H-pyran-2-yl)-15-hydroxy-2,10,12-trimethyl-1,6,8-trioxadispiro[4.1.5.3]pentadec-13-en-9-yl]-2-hydroxy-1,3-dimethyl-4-oxoheptyl]tetrahydro-5-methyl-2H-pyran-2-acetic acid, Salinomycin, Coxistac, Antibiotic 61477. CAS No. 53003-10-4. Pack Sizes: 5MG, 25MG, 50MG. IUPAC Name: (2R)-2-[(2R, 5S, 6R)-6-[(2S, 3S, 4S, 6R)-6-[(3S, 5S, 7R, 9S, 10S, 12R, 15R)-3-[(2R, 5R, 6S)-5-ethyl-5-hydroxy-6-methyloxan-2-yl]-15-hydroxy-3, 10, 12-trimethyl-4, 6, 8-trioxadispiro[4. 1. 5^{7}. 3^{5}]pentadec-13-en-9-yl]-3-hydroxy-4-methyl-5-oxooctan-2-yl]-5-methyloxan-2-yl]butanoic acid. Molecular Formula: C42H70O11. Mole Weight: 751.00. EC Number: 258-290-1. Catalog: APS53003104. Assay: ≥98% (HPLC). SMILES: CC[C@H] ([C@H]1CC[C@H] (C)[C@@H] (O1)[C@@H] (C)[C@H] (O)[C@H] (C)C (=O)[C@H] (CC)[C@H]2O[C@@]3 (O[C@@]4 (CC[C@] (C) (O4)[C@H]5CC[C@] (O) (CC)[C@H] (C)O5)[C@H] (O)C=C3)[C@H] (C)C[C@@H]2C)C (=O)O. Format: Neat. |  |
| Salinomycin | It is an antibiotic produced by the strain of Str. albus 80614. It has anti-gram-positive bacteria and mycobacterium effects. It also has the effect against gram-negative bacteria and fungi but the effect is weak. It has a therapeutic effect on chickens infected with coccidiococci. Synonyms: Procoxacin; Coxistac; AHR 3096; AHR3096; AHR-3096; HSDB 7032; HSDB7032; HSDB-7032; K 364; K364; K-364; Bio-Cox; Sacox; Salocin; 1, ?6, ?8-Trioxadispiro[4. 1. 5. ?3]?pentadecane; Antibiotic 61477; Salinomicina. Grades: 98%. CAS No. 53003-10-4. Molecular formula: C42H70O11. Mole weight: 751.01. | |
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