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| Product | Description | |
|---|---|---|
| barium sulfate | Barium Sulfate. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! Categories: Barium sulphate; BaSO4..top product . |  Texas TX |
| Ammonium sulfates | Our wide distribution network, with locations coast-to-coast, helps guarantee fast, reliable service to Univar's customers. |  |
| 2, 2, 2-tri chloroethoxysulfuryl-N- methyl imidazolium Triflate | A reagent for introduction of 2,2,2-trichloroethyl-protected sulfates into monosaccharides. Group: Biochemicals. Alternative Names: 1-Methyl-3-[ (2, 2, 2-trichloroethoxy) sulfonyl]-1H-imidazolium 1, 1, 1-Trifluoromethane sulfonate. Grades: Highly Purified. CAS No. 903587-97-3. Pack Sizes: 25mg. US Biological Life Sciences. |  Worldwide |
| Boc-D-cysteine | Boc-D-cysteine is an N-Boc-protected form of D-Cysteine. D-Cysteine is a strong inhibitor of Escherichia coli growth and also functions to provide inorganic sulfates for the sulfation of xenobiotics. D-Cysteine is a non-physiological isomer of L-Cysteine, and is not involved in protein or glutathione synthesis. Synonyms: Boc-D-Cys-OH; N-Boc-D-cysteine; Boc-D-cysteine; (S)-2-((tert-Butoxycarbonyl)amino)-3-mercaptopropanoic acid; D-Cysteine, N-[(1,1-dimethylethoxy)carbonyl]-; (tert-Butoxycarbonyl)-D-cysteine; Boc-D-Cys-OH; (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-sulfanylpropanoic acid; AmbotzBAA1170; N-[(1,1-dimethylethoxy)carbonyl]-D-cysteine; Boc D Cys OH. Grades: ≥ 99% (Assay by titration). CAS No. 149270-12-2. Molecular formula: C8H15NO4S. Mole weight: 221.30. |  |
| cerebroside-sulfatase | Hydrolyses galactose-3-sulfate residues in a number of lipids. Also hydrolyses ascorbate 2-sulfate and many phenol sulfates. Group: Enzymes. Synonyms: arylsulfatase A; cerebroside sulfate sulfatase. Enzyme Commission Number: EC 3.1.6.8. CAS No. 9068-68-2. 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-3758; cerebroside-sulfatase; EC 3.1.6.8; 9068-68-2; arylsulfatase A; cerebroside sulfate sulfatase. Cat No: EXWM-3758. |  |
| Cetylpyridinium Chloride, Monohydrate, USP | Hexadecylpyridinium Chloride. SDS mixture of sodium alkyl sulfates consisting chiefly of sodium lauryl sulfate. Grades: USP. CAS No. 6004-24-6. Product ID: 8-01596. Molecular formula: C21H38NCl H2O. Mole weight: 358.00 . |  |
| chondro-4-sulfatase | Also acts on the saturated analogue but not on higher oligosaccharides, nor any 6-sulfates. Group: Enzymes. Synonyms: chondroitin-4-sulfatase; 4-deoxy-β-D-gluc-4-enuronosyl-(1,3)-N-acetyl-D-galactosamine-4-sulfate 4-sulfohydrolase. Enzyme Commission Number: EC 3.1.6.9. CAS No. 9045-75-4. 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-3759; chondro-4-sulfatase; EC 3.1.6.9; 9045-75-4; chondroitin-4-sulfatase; 4-deoxy-β-D-gluc-4-enuronosyl-(1,3)-N-acetyl-D-galactosamine-4-sulfate 4-sulfohydrolase. Cat No: EXWM-3759. | |
| Chondroitin-4-sulfate sodium salt | chondroitin sulfate A. CAS No. 39455-18-0. Product ID: 4-00054. Purity: 85.0+%. Properties: Also available: fractionated dermatan sulfates with Av. Mw 25,000 ± 2,500 and 50,000 ± 5,000 and different Anti-Xa and Anti-IIa activities. Please inquire. Reference: Low-Molecular Weight Heparins in Prophylaxis and Therapy of Thromboembolic Diseases, H. Bounameaux, ed., Marcel-Dekker, New York, 1995; Biomimetic Polymers, Linhardt, R. J, Loganathan, D., Plenum Press, New York, 1990; Ann. NY Acad. Sci., 556, 468, 1989. | |
| Chondroitinase ABC from Proteus vulgaris, Recombinant | Chondroitinase ABC cleaves, via an elimination mechanism, sulfated and non-sulfated polysaccharide chains containing 1-4 linkages between hexosamines and glucuronic acid residues. The reaction yields oligosaccharide products (mainly disaccharides) containing unsaturated uronic acids which can be detected by UV spectroscopy at 232 nm. The enzyme is active on chondroitin sulfates A and C, chondroitin sulfates B (dermatan sulfate), chondroitin and hyaluronic acid. Applications: Determination of contents of chondroitin sulfates by hplcprocessing animal tissues before further investigationspreparation of chondroitin and hyaluronic acid derived unsaturated disaccharidespreparation of hyaluronic acid derived unsaturated disaccharide. Group: Enzymes. Synonyms: EC 4.2.2.4, chondroitinase; ch. Enzyme Commission Number: EC 4.2.2.20. CAS No. 9024-13-9. Chondroitinase ABC. Mole weight: 117.3 kDa. Activity: > 100 IU/mg (substrate: chondroitin sulfate A). Stability: Expiration is at least 12 months from manufacturing date, kept at -20 °C. Source: E.coli. Species: Proteus vulgaris. EC 4.2.2.4, chondroitinase; chondroitin ABC eliminase; chondroitinase ABC; chondroitin ABC lyase; chondroitin sulfate ABC lyase; ChS ABC lyase; chondroitin sulfate ABC endoeliminase; chondroitin sulfate ABC endolyase; ChS ABC lyase I; 9024-13-9. Cat No: NATE-1949. | |
| Chondroitinase AC from Flavobacterium heparinum, Recombinant | Chondroitinase AC from Flavobacteriun heparinum is an eliminase that degrades chondroitin sulfates A and C, but not chondroitin sulfate B. The enzyme cleaves, via an elimination mechanism, both sulfated and non-sulfated polysaccharide chains that contain (1?4)-linkages between hexosamines and glucuronic acid residues. The reaction yields oligosaccharide products, mainly disaccharides, with unsaturated uronic acids that can be detected by UV spectroscopy at 232 nm. Applications: Chondroitinase ac was shown to inhibit melanoma invasion and proliferation, endothelial proliferation, and angiogenesis. chondroitinase ac, but not chondroitinase b, has also been shown t..., and protease activities. ChnAC. Activity: >200 units/mg protein. Appearance: Powder. Storage: Store the product at -20?C. When stored properly and unopened at -20?C, the enzyme has a recommended retest date of 2 years. After reconstitution, the product may be kept at 4?C for 4 days, but it is recommended to store the solution in working aliquots at -20 ?C. Form: The enzyme is supplied as a lyophilized powder containing potassium phosphate, NaCl, and a stabilizer. Source: E. coli. Species: Flavobacterium heparinum. chondroitinase (ambiguous); chondroitin sulfate lyase; chondroitin AC eliminase; chondroitinase AC; ChnAC; 9047-57-8; EC 4.2.2.5. Cat No: NATE-1738. | |
| Chondroitin disaccharide Δdi-6S disodium salt | It is produced by various chondroitin sulfates through the action of chondroitin enzymes ABC, AC-1 and C. Synonyms: Disodium 2-acetamido-2-deoxy-3-O-(4-deoxy-L-threo-hex-4-enopyranuronosyl)-6-O-sulfonato-D-galactopyranose; Alpha-delta-ua-[1->3]-galnac-6s sodium salt; Chondroitin disaccharide delta-di-6S sodium salt; sodium (3R,4S)-2-((3R,4R,5R,6R)-3-acetamido-2,5-dihydroxy-6-(sulfonatooxymethyl)tetrahydro-2H-pyran-4-yloxy)-3,4-dihydroxy-3,4-dihydro-2H-pyran-6-carboxylate; D-Galactopyranose, 2-(acetylamino)-2-deoxy-3-O-(4-deoxy-L-threo-hex-4-enopyranuronosyl)-, 6-(hydrogen sulfate), sodium salt (1:2). Grades: ≥98%. CAS No. 136132-72-4. Molecular formula: C14H19NNa2O14S. Mole weight: 503.34. | |
| Chondroitin disaccharide di-0S sodium salt | It is produced by various chondroitin sulfates through the action of chondroitin enzymes ABC, AC-1 and C. Synonyms: D-Galactose, 2-(acetylamino)-2-deoxy-3-O-(4-deoxy-alpha-L-threo-hex-4-enopyranuronosyl)-, monosodium salt; 2-Acetamido-2-deoxy-3-O-(b-D-gluco-4-enepyranosyl uronic acid)-D-galactose sodium salt; GlcAb(1-4)GalNAc; α-ΔUA-[1?3]-GalNAc. Grades: ≥95%. CAS No. 136132-69-9. Molecular formula: C14H20NNaO11. Mole weight: 401.30. | |
| Chondroitin disaccharide di-diSB trisodium salt | It is produced from various chondroitin sulfates by the action of chondroitin enzymes ABC and/or B, and most typically from chondroitin sulfate B (dermatan sulfate). Synonyms: Chondroitin disaccharide (delta-DiSB, sodium salt); 2-Acetamido-2-deoxy-3-O-(2-O-sulfo-beta-D-gluco-4-enepyranosyluronic acid)-4-O-sulfo-D-galactose sodium salt; sodium (3R,4S)-2-((3R,4R,5R,6R)-3-acetamido-2-hydroxy-6-(hydroxymethyl)-5-(sulfonatooxy)tetrahydro-2H-pyran-4-yloxy)-4-hydroxy-3-(sulfonatooxy)-3,4-dihydro-2H-pyran-6-carboxylate. Grades: ≥90%. CAS No. 136132-71-3. Molecular formula: C14H18NNa3O17S2. Mole weight: 605.39. | |
| Chondroitin disaccharide di-diSD trisodium salt | It is produced by various chondroitin sulfates through the action of chondroitin enzyme ABC. Synonyms: Chondroitin disaccharide Δdi-disD Disodium Salt. Grades: ≥95%. CAS No. 149368-03-6. Molecular formula: C14H18NO17S2Na3. Mole weight: 605.39. | |
| Chondroitine sulfate | Chondroitin sulfate can be found in the Shark cartilage. Chondroitin is in dietary supplements used as an alternative medicine to treat osteoarthritis and also approved and regulated as a symptomatic slow-acting drug for this disease (SYSADOA) in Europe and some other countries. The hydrolysis and transglycosylation reactions of bovine testicular hyaluronidase were dose-dependently inhibited by Chondroitin sulfate oligosaccharides. Uses: Antihyperlipemic. Synonyms: poly-1(2/3)-n-acetyl-2-amino-2-deoxy-3-o-beta-d-glucopyranurosyl-4-(6)sulfonyl-d-galactose; chondroitinpolysulfate; chondroitinsulfates; chondroitinsulfuricacid; chondroitinsulfuricacids; chonsurid; CHONDROITIN SULPHATE; CHONDROITINE SULPHATE. Grades: >90%. CAS No. 9007-28-7. Molecular formula: (C14H21NO14S)n. Mole weight: 463.37. | |
| D-Cysteine | D-Cysteine is a strong inhibitor of Escherichia coli growth and also functions to provide inorganic sulfates for the sulfation of xenobiotics. D-Cysteine is a non-physiological isomer of L-Cysteine, and is not involved in protein or glutathione synthesis. Synonyms: (S)-Cysteine; (S)-2-amino-3-mercaptopropanoic acid; D-Zystein; D-Amino-3-mercaptopropionic acid; D-Cys; (2S)-2-amino-3-mercaptopropanoic acid. Grades: ≥97%. CAS No. 921-01-7. Molecular formula: C3H7NO2S. Mole weight: 121.16. | |
| Dermatan sulfate | chondroitin sulfate B from porcine intestinal mucosa[uronic acid-b-1,4-N-acetyl-D-galactosamine]n. CAS No. 54328-33-5. Product ID: 4-00055. Mole weight: Av. Mw 30,000. Purity: Anti-IIa activity >5 units/mg. Properties: Also available fractionated heparan sulfates with lower molecular weights and different Anti-IIa activities. Source : porcine. | |
| Dysprosium Sulfide | Dysprosium Sulfide is a moderately water and acid soluble Dysprosium source for uses compatible with sulfates. Sulfate compounds are salts or esters of sulfuric acid formed by replacing one or both of the hydrogens with a metal. Most metal sulfate compounds are readily soluble in water for uses such as water treatment, unlike fluorides and oxides which tend to be insoluble. Uses: Designed for use in research and industrial production. Additional or Alternative Names: DYSPROSIUM SULFIDE;DYSPROSIUM SULFIDE 99.9%. Product Category: Heterocyclic Organic Compound. Appearance: Powder. CAS No. 12133-06-1. Molecular formula: DyS. Mole weight: 195g/mol. Product ID: ACM12133061. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Erbium Sulfide | Erbium Sulfide is a moderately water and acid soluble Erbium source for uses compatible with sulfates. Uses: Designed for use in research and industrial production. Additional or Alternative Names: ERBIUM SULFIDE;dierbium trisulphide;ERBIUM SULFIDE 99.9%;ERBIUM SULPHIDE;Erbium sulfide, min. 99% powder;Erbium sulfide, 99.9% (REO). Product Category: Heterocyclic Organic Compound. Appearance: Powder. CAS No. 12159-66-9. Molecular formula: Er2S3. Mole weight: 431g/mol. Purity: 0.96. IUPACName: erbium(3+) trisulfide. Density: 6.07g/mL. Product ID: ACM12159669. Alfa Chemistry ISO 9001:2015 Certified. Categories: Erbium sulfide (Er2S3). | |
| Fmoc-D-cysteine | Fmoc-D-cysteine is an N-Fmoc-protected form of D-Cysteine. D-Cysteine is a strong inhibitor of Escherichia coli growth and also functions to provide inorganic sulfates for the sulfation of xenobiotics. D-Cysteine is a non-physiological isomer of L-Cysteine, and is not involved in protein or glutathione synthesis. Synonyms: N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-cysteine; Fmoc-L-Cys-OH; Fmoc-cysteine; N-(9-Fluorenylmethoxycarbonyl)cysteine. Grades: 96%. CAS No. 157355-80-1. Molecular formula: C18H17NO4S. Mole weight: 343.40. | |
| Fucoidan | Fucoidan is a fucan sulfate present in brown marine algae (Phaeophyta, typically Ascophyllum nodosum and Laminaria digitata) and has anticoagulant activity. The main constituents are α(1-4) and α(1-2) linked L-focus sulfates, although galactose also occurs and there are many variations of the basic structure found in different species of Phaeophyta. | |
| galactosylgalactosylxylosylprotein 3-β-glucuronosyltransferase | Involved in the biosynthesis of the linkage region of glycosaminoglycan chains as part of proteoglycan biosynthesis (chondroitin, dermatan and heparan sulfates). Requires Mn2+. Group: Enzymes. Synonyms: glucuronosyltransferase I; uridine diphosphate glucuronic acid:acceptor glucuronosyltransferase; UDP-glucuronate:3-β-D-galactosyl-4-β-D-galactosyl-O-β-D-xylosyl-protein D-glucuronosyltransferase; UDP-glucuronate:3-β-D-galactosyl-4-β-D-galactosyl-O-β-D-xylosylprotein D-glucuronosyltransferase. Enzyme Commission Number: EC 2.4.1.135. CAS No. 227184-75-0. 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-2360; galactosylgalactosylxylosylprotein 3-β-glucuronosyltransferase; EC 2.4.1.135; 227184-75-0; glucuronosyltransferase I; uridine diphosphate glucuronic acid:acceptor glucuronosyltransferase; UDP-glucuronate:3-β-D-galactosyl-4-β-D-galactosyl-O-β-D-xylosyl-protein D-glucuronosyltransferase; UDP-glucuronate:3-β-D-galactosyl-4-β-D-galactosyl-O-β-D-xylosylprotein D-glucuronosyltransferase. Cat No: EXWM-2360. | |
| galactosylxylosylprotein 3-β-galactosyltransferase | Involved in the biosynthesis of the linkage region of glycosaminoglycan chains as part of proteoglycan biosynthesis (chondroitin, dermatan and heparan sulfates). Requires Mn2+. Group: Enzymes. Synonyms: galactosyltransferase II; uridine diphosphogalactose-galactosylxylose galactosyltransferase; UDP-galactose:4-β-D-galactosyl-O-β-D-xylosylprotein 3-β-D-galactosyltransferase; UDP-α-D-galactose:4-β-D-galactosyl-O-β-D-xylosylprotein 3-β-D-galactosyltransferase. Enzyme Commission Number: EC 2.4.1.134. CAS No. 56626-21-2, 56626-19-8. 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-2359; galactosylxylosylprotein 3-β-galactosyltransferase; EC 2.4.1.134; 56626-21-2, 56626-19-8; galactosyltransferase II; uridine diphosphogalactose-galactosylxylose galactosyltransferase; UDP-galactose:4-β-D-galactosyl-O-β-D-xylosylprotein 3-β-D-galactosyltransferase; UDP-α-D-galactose:4-β-D-galactosyl-O-β-D-xylosylprotein 3-β-D-galactosyltransferase. Cat No: EXWM-2359. | |
| glucuronylgalactosylproteoglycan 4-β-N-acetylgalactosaminyltransferase | Requires Mn2+. Involved in the biosynthesis of chondroitin sulfate. Key enzyme activity for the initiation of chondroitin and dermatan sulfates, transferring GalNAc to the GlcA-Gal-Gal-Xyl-Ser core. Group: Enzymes. Synonyms: N-acetylgalactosaminyltransferase I; glucuronylgalactosylproteoglycan β-1,4-N-acetylgalactosaminyltransferase; uridine diphosphoacetylgalactosamine-chondroitin acetylgalactosaminyltransferase I; UDP-N-acetyl-D-galactosamine:D-glucuronyl-1,3-β-D-galactosyl-proteoglycan β-1,4-N-acetylgalactosaminyltransferase; UD. Enzyme Commission Number: EC 2.4.1.174. CAS No. 96189-39-8. 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-2399; glucuronylgalactosylproteoglycan 4-β-N-acetylgalactosaminyltransferase; EC 2.4.1.174; 96189-39-8; N-acetylgalactosaminyltransferase I; glucuronylgalactosylproteoglycan β-1,4-N-acetylgalactosaminyltransferase; uridine diphosphoacetylgalactosamine-chondroitin acetylgalactosaminyltransferase I; UDP-N-acetyl-D-galactosamine:D-glucuronyl-1,3-β-D-galactosyl-proteoglycan β-1,4-N-acetylgalactosaminyltransferase; UDP-N-acetyl-D-galactosamine:D-glucuronyl-(1?3)-β-D-galactosyl-proteoglycan 4-β-N-acetylgalactosaminyltransferase. Cat No: EXWM-2399. | |
| glycochenodeoxycholate sulfotransferase | The enzyme specifically sulfates glycochenodeoxycholate at the 7α-position (see also EC 2.8.2.14 bile-salt sulfotransferase). The monohydroxy bile acids glycolithocholate, chenodeoxycholate and ursodeoxycholate act as inhibitors. Group: Enzymes. Synonyms: bile acid:3'-phosphoadenosine-5'-phosphosulfate sulfotransferase; bile acid:PAPS:sulfotransferase; BAST. Enzyme Commission Number: EC 2.8.2.34. CAS No. 72668-90-7. 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-3394; glycochenodeoxycholate sulfotransferase; EC 2.8.2.34; 72668-90-7; bile acid:3'-phosphoadenosine-5'-phosphosulfate sulfotransferase; bile acid:PAPS:sulfotransferase; BAST. Cat No: EXWM-3394. | |
| glycosulfatase | Also acts on other sulfates of monosaccharides and disaccharides and on adenosine 5'-sulfate. Group: Enzymes. Synonyms: glucosulfatase. Enzyme Commission Number: EC 3.1.6.3. CAS No. 9025-61-0. 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-3754; glycosulfatase; EC 3.1.6.3; 9025-61-0; glucosulfatase. Cat No: EXWM-3754. | |
| [heparan sulfate]-glucosamine 3-sulfotransferase 2 | This enzyme sulfates the residues marked with an asterisk in sequences containing at least ? IdoA2S? GlcN*? or ? GlcA2S? GlcN*? (symbols as in 2-Carb-38). Preference for GlcN2S vs. unmodified GlcN has not yet been established. Additional structural features are presumably required for substrate recognition, since the 3-O-sulfated residue is of low abundance, whereas the above IdoA-containing sequence is quite abundant. This enzyme differs from the other [heparan sulfate]-glucosamine 3-sulfotransferases by modifying selected glucosamine residues preceded by GlcA2S; EC 2.8.2.23 ([heparan sulfate]-glucosamine 3-sulfotransferase 1) prefers GlcA or IdoA, whereas EC 2.8.2.30 ([heparan sulfate]-glucosamine 3-sulfotransferase 3) prefers IdoA2S. Group: Enzymes. Synonyms: glucosaminyl 3-O-sulfotransferase; heparan sulfate D-glucosaminyl 3-O-sulfotransferase; isoform/isozyme 2 (3-OST-2, HS3ST2). Enzyme Commission Number: EC 2.8.2.29. 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-3388; [heparan sulfate]-glucosamine 3-sulfotransferase 2; EC 2.8.2.29; glucosaminyl 3-O-sulfotransferase; heparan sulfate D-glucosaminyl 3-O-sulfotransferase; isoform/isozyme 2 (3-OST-2, HS3ST2). Cat No: EXWM-3388. | |
| hyaluronoglucosaminidase | Also hydrolyses 1,4-β-D-glycosidic linkages between N-acetyl-galactosamine or N-acetylgalactosamine sulfate and glucuronic acid in chondroitin, chondroitin 4- and 6-sulfates, and dermatan. Group: Enzymes. Synonyms: hyaluronidase; hyaluronoglucosidase; chondroitinase; chondroitinase I. Enzyme Commission Number: EC 3.2.1.35. CAS No. 37326-33-3. Hyaluronidase. 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-3897; hyaluronoglucosaminidase; EC 3.2.1.35; 37326-33-3; hyaluronidase; hyaluronoglucosidase; chondroitinase; chondroitinase I. Cat No: EXWM-3897. | |
| Iron Disulfide | Iron Sulfide is a moderately water and acid soluble Iron source for uses compatible with sulfates. Sulfate compounds are salts or esters of sulfuric acid formed by replacing one or both of the hydrogens with a metal. Group: Nanoparticlesbattery materials. Alternative Names: Iron(II) disulfide, Ferrous disulfide, Iron disulphide, Marcasite (CAS 1317-66-4), Hydropyrite, Iron(2+) disulfide, 23949-99-7, 58440-06-5. CAS No. 12068-85-8. Product ID: bis(sulfanylidene)iron. Molecular formula: 119.97499999999999. Mole weight: FeS2. S=[Fe]=S. InChI=1S/Fe.S2/c;1-2/q+2;-2. NIFIFKQPDTWWGU-UHFFFAOYSA-N. 0.99999000000000005. |  |
| Irosustat | Irosustat, also known as STX64, BN83495 and 667 coumate, is a potent, irreversible inhibitor of steroid sulfatase. Inhibition of steroid sulfatase (STS), the enzyme responsible for the hydrolysis of steroid sulfates, represents a potential novel treatment for postmenopausal women with hormone-dependent breast cancer. Estrone and DHEA are formed by this sulfatase pathway and can be converted to steroids (estradiol and androstenediol, respectively), which have potent estrogenic properties. STX64 (667 coumate) is a potent tricylic coumarin-based sulfamate that irreversibly inhibits STS activity (IC50= 8 nM in a placental microsomal assay system). Estrone sulfamate (EMATE) is also a potent STS inhibitor, but has estrogenic activity. Synonyms: BN83495; BN-83495; BN 83495; STX 64; STX-64; STX64; 667-Coumate; Sulfamic acid, 6,7,8,9,10,11-hexahydro-6-oxobenzo[b]cyclohepta[d]pyran-3-yl ester. CAS No. 288628-05-7. Molecular formula: C14H15NO5S. Mole weight: 309.34. | |
| κ-carrageenan | Carrageenan is a hydrophilic colloid that is extracted from red algae seaweeds such as unicornia, celery, and carrageen. Their chemical structures are calcium, potassium, sodium and ammonium salts of polysaccharide sulfates composed of galactose and anhydrogalactose. Carrageenan can be divided into 7 types, including K-type (Kappa), I-type (Iota), and L-type (Lambda), according to the different positions where the half-ester sulfate group is attached to galactose. The gel properties of carrageenan are mainly related to its chemical composition, structure and molecular size. Based on the properties of carrageenan, they are widely used in the food industry, medicine and other fields. Uses: ·adhesives, thickeners, emulsifiers and stabilizers in the food industry ·culture medium, medicament, anticoagulant, hypolipidemic agent and laxative in the field of medicine ·used as an antistatic agent for photosensitive emulsions and photosensitive emulsion layers ·embedding material for immobilized enzyme carrier and bacteria ·for leather industry, ceramic industry, textile industry and paper. Group: Polysaccharidepolymers. CAS No. 11114-20-8. Product ID: [(2R,3S,4R,5R,6S)-6-[[(1R,3S,4R,5R,8S)-3,4-dihydroxy-2,6-dioxabicyclo[3.2.1]octan-8-yl]oxy]-4-[[(1R,3R,4R,5R,8S)-8-[(2S,3R,4R,5R,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-sulfonatooxyoxan-2-yl]oxy-4-hydroxy-2,6-dioxabicyclo[3.2.1]octan-3-yl]oxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] | |
| Lactosamine | Lactosamine forms the backbone of several cell surface glycans such as sialylated glycans or keratin sulfates. Also, it is a basic structural element of Lewis type, and human milk oligosaccharides. Group: Biochemicals. Grades: Highly Purified. CAS No. 13000-25-4. Pack Sizes: 5mg, 10mg. Molecular Formula: C12H23NO10, Molecular Weight: 341.31. US Biological Life Sciences. | Worldwide |
| Native Abalone Sulfatase | Sulfatases EC 3.1.6.1 are enzymes of the esterase class that catalyze the hydrolysis of sulfate esters. These may be found on a range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. In the latter case the resultant N-sulfates can also be termed sulfamates. Sulfatases play important roles in the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodelling sulfated glycosaminoglycans in the extracellular space. Together with sulfotransferases, sulfatases form the major catalytic machinery for the synthesis and breakage of sulfa...ne conjugates from hamster embryo fibroblasts. Group: Enzymes. Synonyms: EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Enzyme Commission Number: EC 3.1.6.1. CAS No. 9016-17-5. Sulfatases. Activity: 20-40 units/mg solid. Storage: -20°C. Form: lyophilized powder. Source: Abalone entrails. Species: Abalone. EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Cat No: NATE-0685. | |
| Native Aerobacter aerogenes Sulfatase | Sulfatases EC 3.1.6.1 are enzymes of the esterase class that catalyze the hydrolysis of sulfate esters. These may be found on a range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. In the latter case the resultant N-sulfates can also be termed sulfamates. Sulfatases play important roles in the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodelling sulfated glycosaminoglycans in the extracellular space. Together with sulfotransferases, sulfatases form the major catalytic machinery for the synthesis and breakage o...17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Enzyme Commission Number: EC 3.1.6.1. CAS No. 9016-17-5. Sulfatases. Activity: 2-5 units/mg protein (biuret), 10-20 units/mL. Storage: -20°C. Form: buffered aqueous glycerol solution; Solution in 50% glycerol containing 0.01 M Tris, pH 7.5. Source: Aerobacter aerogenes. EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Cat No: NATE-0686. | |
| Native Bovine Hyaluronidase | Hyaluronidase degrades hyaluronan and has been found to be inappropriately regulated during cancer progression. These enzymes randomly cleave β-N-acetylhexosamine-[1?4] glycosidic bonds in hyaluronic acid, chondroitin, and chondroitin sulfates. Group: Enzymes. Synonyms: hyaluronoglucosaminidase; hyaluronidase; hyaluronoglucosidase; chondroitinase; chondroitinase I; hyaluronate 4-glycanohydrolase; EC 3.2.1.35; 37326-33-3. Enzyme Commission Number: EC 3.2.1.35. CAS No. 37326-33-3. Hyaluronidase. Mole weight: mol wt ~55 kDa (four subunits of 14 kDa each). Activity: Type I, 750-3000 units/mg solid; Type II, 300-1,000 units/mg; Type III, 3,000-15,000 units/mg solid; Type IV, 400-1000 units/mg solid. Storage: -20°C. Form: lyophilized powder. Source: Bovine testes. Species: Bovine. hyaluronoglucosaminidase; hyaluronidase; hyaluronoglucosidase; chondroitinase; chondroitinase I; hyaluronate 4-glycanohydrolase; EC 3.2.1.35; 37326-33-3. Cat No: NATE-0347. | |
| Native Flavobacterium heparinum Chondroitinase AC | Chondroitinase AC from Flavobacterium heparinum is an enzyme that cleaves sulfated and non-sulfated polysaccharide chains with (1-4) linkages between hexosamines and glucuronic acid residues, by an elimination mechanism. The resulting oligosaccharide products are mainly disaccharides with unsatuRated uronic acids. Chondroitinase AC specifically degrades chondroitin sulfates A and C, but not chondroitin sulfate B (dermatan sulfate). Applications: Chondroitinase ac from creative enzymes has been used for the large scale preparation of glycosaminoglycan (gag) fractions during the study of structural and sequence motifs in dermatan sulfate. Group: Enzymes. Synonyms: EC 4.2.2.5; 9047-57-8; chondroitin AC lyase; chondroitinase; chondroitin sulfate lyase; chondroitin AC eliminase; chondroitin AC lyase; chondroitinase AC; ChnAC. Enzyme Commission Number: EC 4.2.2.5. CAS No. 9047-57-8. ChnAC. Activity: 0.5-1.5 units/mg solid (using chondroitin sulfate A as substrate, also cleaves chondroitin sulfate C). Storage: -20°C. Form: lyophilized powder. Source: Flavobacterium heparinum. EC 4.2.2.5; 9047-57-8; chondroitin AC lyase; chondroitinase; chondroitin sulfate lyase; chondroitin AC eliminase; chondroitin AC lyase; chondroitinase AC; ChnAC. Cat No: NATE-0126. | |
| Native Flavobacterium heparinum Chondroitinase B | Chondroitinase B cleaves, via an elimination mechanism, polysaccharide chains containing 1-4 linkages between hexosamines and iduronic acid residues in dermatan sulfate (chondroitin B).The reaction yields oligosaccharide products (mainly disaccharides) containing unsaturated uronic acids which can be detected by UV spectroscopy at 232 nm. Applications: Research reagent (glycobiology, preparation of oligosaccharide libraries from dermatan sulfate).determination of contents of chondrotin sulfates by hplc. Group: Enzymes. Synonyms: Chondroitinase B; EC 4.2.2.19; chondroitin B lyase; ChonB; ChnB. Enzyme Commission Number: EC 4.2.2.19. CAS No. 52227-83-5. ChonB. Mole weight: 55 kDa. Activity: >200 IU/mg (substrate: dermatan sulfate). Stability: 12 months frozen at -20°C in aqueous buffers containing sodium phosphate and sucrose 5%. Source: Flavobacterium heparinum. Chondroitinase B; EC 4.2.2.19; chondroitin B lyase; ChonB; ChnB. Cat No: NATE-1950. | |
| Native Helix pomatia Sulfatase | Sulfatases EC 3.1.6.1 are enzymes of the esterase class that catalyze the hydrolysis of sulfate esters. These may be found on a range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. In the latter case the resultant N-sulfates can also be termed sulfamates. Sulfatases play important roles in the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodelling sulfated glycosaminoglycans in the extracellular space. Together with sulfotransferases, sulfatases form the major catalytic machinery for the synthesis and breakage of su...n. Group: Enzymes. Synonyms: EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Enzyme Commission Number: EC 3.1.6.1. CAS No. 9016-17-5. Sulfatases. Activity: Type I, > 10 ,000 units/g solid; Type II, > 2 ,000 units/mL. Storage: -20°C. Form: Type I, powder; Type II, aqueous solution. Source: Helix pomatia. EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Cat No: NATE-0687. | |
| Native Human Tryptase | Tryptase is a member of the serine protease S1 family. It is the predominant neutral protease of the mast cell granules. Within the mast cell granule it exists as a heparin-stabilized active tetramer. Stabilization is a result of the high negative charge density of the glycosaminoglycan. This stabilization activity is observed with heparins with a MW > 6 kDa as well as other glycosaminoglycans such as dextran sulfate or chondroitin sulfates. Removal of heparin results in dissociation of the tetramer and inactivation of the enzyme. High concentrations of NaCl will result in the dissociation of heparin. Tryptase is a glycoprotein released from mast cells during anaphylaxis, which pe...acterized recombinant rat mast cell protease 7 expressed in pichia pastoris. tryptase has also been used in a study to investigate drug allergies in mast cell disease. Group: Enzymes. Synonyms: tryptase; mast cell tryptase; mast cell protease II; skin tryptase; lung tryptase; pituitary tryptase; mast cell neutral proteinase; mast cell tryptase; mast cell neutral proteinase; mast cell serine proteinase II; mast cell proteinase II; mast cell serine proteinase tryptase; rat mast cell protease II; tryptase M; EC 3.4.21.59. Enzyme Commission Number: EC 3.4.21.59. CAS No. 97501-93-4. Tryptase. Mole weight: Molecular Weight: ~135 kDa (Human) (Non-covalently linked tetramer with two sets o | |
| Native Patella vulgata (keyhole limpet) Sulfatase | Sulfatases EC 3.1.6.1 are enzymes of the esterase class that catalyze the hydrolysis of sulfate esters. These may be found on a range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. In the latter case the resultant N-sulfates can also be termed sulfamates. Sulfatases play important roles in the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodelling sulfated glycosaminoglycans in the extracellular space. Together with sulfotransferases, sulfatases form the major catalytic machinery for the synthesis and breakage of sulfate esters. Group: Enzymes. Synonyms: EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbellifery. Enzyme Commission Number: EC 3.1.6.1. CAS No. 9016-17-5. Sulfatases. Activity: Type I, > 10 units/mg solid; Type II, > 5 units/mg solid. Storage: -20°C. Form: essentially salt-free, lyophilized powder. Source: Patella vulgata (keyhole limpet). EC 3.1.6.1; 9016-17-5; sulfatase; nitrocatechol sulfatase; phenolsulfatase; phenylsulfatase; p-nitrophenyl sulfatase; arylsulfohydrolase; 4-methylumbelliferyl sulfatase; estrogen sulfatase; arylsulfatase. Cat No: NATE-0688. | |
| Native Sheep Hyaluronidase | Hyaluronidase degrades hyaluronan and has been found to be inappropriately regulated during cancer progression. These enzymes randomly cleave β-N-acetylhexosamine-[1?4] glycosidic bonds in hyaluronic acid, chondroitin, and chondroitin sulfates. Group: Enzymes. Synonyms: hyaluronoglucosaminidase; hyaluronidase; hyaluronoglucosidase; chondroitinase; chondroitinase I; hyaluronate 4-glycanohydrolase; EC 3.2.1.35; 37326-33-3. Enzyme Commission Number: EC 3.2.1.35. CAS No. 37326-33-3. Hyaluronidase. Mole weight: mol wt 55 kDa. Activity: Type I, > 1,500 units/mg solid; Type II, > 300 units/mg solid. Storage: -20°C. Form: Type I, lyophilized powder; Type II, Lyophilized powder containing lactose. Source: Sheep testes. Species: Sheep. hyaluronoglucosaminidase; hyaluronidase; hyaluronoglucosidase; chondroitinase; chondroitinase I; hyaluronate 4-glycanohydrolase; EC 3.2.1.35; 37326-33-3. Cat No: NATE-0348. | |
| Native Streptomyces hyalurolyticus Hyaluronidase | Hyaluronidase degrades hyaluronan and has been found to be inappropriately regulated during cancer progression. These enzymes randomly cleave β-N-acetylhexosamine-[1?4] glycosidic bonds in hyaluronic acid, chondroitin, and chondroitin sulfates. Group: Enzymes. Synonyms: hyaluronoglucosaminidase; hyaluronidase; hyaluronoglucosidase; chondroitinase; chondroitinase I; hyaluronate 4-glycanohydrolase; EC 3.2.1.35; 37326-33-3. Enzyme Commission Number: EC 3.2.1.35. CAS No. 37326-33-3. Hyaluronidase. Activity: Type I, > 1,500 units/mg solid; Type II, > 300 units/mg solid. Storage: -20°C. Form: lyophilized powder. Source: Streptomyces hyalurolyticus. hyaluronoglucosaminidase; hyaluronidase; hyaluronoglucosidase; chondroitinase; chondroitinase I; hyaluronate 4-glycanohydrolase; EC 3.2.1.35; 37326-33-3. Pack: ampule of 300 × units. Cat No: NATE-0349. | |
| Potassium sulfate | Potassium sulfate. CAS No. 7778-80-5. Pack Sizes: 500 g in poly bottle. Product ID: CDC10-0239. Molecular formula: K2O4S. Category: Buffering Agents. Product Keywords: Cosmetic Ingredients; Buffering Agents; Potassium sulfate; CDC10-0239; 7778-80-5; K2O4S; 231-915-5; MFCD00011388; 7778-80-5. Purity: 0.98. Color: White Crystalline. EC Number: 231-915-5. Physical State: Powder. Quality Level: 200. Storage: Store at RT. Boiling Point: 1689°C. Melting Point: 1067°C. Density: 2.662 g/cm3. Product Description: Potassium sulfate (K2SO4)is a colorless compound having rhombic or hexagonal crystals. It readily forms double salts with the sulfate of trivalent metals, which are known as Alums. It also forms double salts with calcium, magnesium and sodium sulfates. It is widely employed as a fertilizer. K2SO4 can be extracted from various complex salts in nature, such as Kainite, langbeinite and carpathein mineral ores. It can be synthesized by reacting KCl and sulfuric acid, via Mannheim process. |  |
| Protamine sulfate | Protamine sulfate is used as an antidote against the anticoagulant effects of negatively charged heparin, for example in heart surgery. Synonyms: Protamines, sulfates; Novo protamine sulfate; Protamine sulfates. Grades: 95%. CAS No. 9009-65-8. | |
| protein xylosyltransferase | Involved in the biosynthesis of the linkage region of glycosaminoglycan chains as part of proteoglycan biosynthesis (chondroitin, dermatan and heparan sulfates). Group: Enzymes. Synonyms: UDP-D-xylose:core protein β-D-xylosyltransferase; UDP-D-xylose:core protein xylosyltransferase; UDP-D-xylose:proteoglycan core protein β-D-xylosyltransferase; UDP-xylose-core protein β-D-xylosyltransferase; uridine diphosphoxylose-core protein β-xylosyltransferase; uridine diphosphoxylose-protein xylosyltransferase. Enzyme Commission Number: EC 2.4.2.26. CAS No. 55576-38-0. 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-2653; protein xylosyltransferase; EC 2.4.2.26; 55576-38-0; UDP-D-xylose:core protein β-D-xylosyltransferase; UDP-D-xylose:core protein xylosyltransferase; UDP-D-xylose:proteoglycan core protein β-D-xylosyltransferase; UDP-xylose-core protein β-D-xylosyltransferase; uridine diphosphoxylose-core protein β-xylosyltransferase; uridine diphosphoxylose-protein xylosyltransferase. Cat No: EXWM-2653. | |
| (R)-specific secondary-alkylsulfatase | The enzyme from Rhodococcus ruber is involved in the biodegradation of alkyl sulfate esters used as detergents and released into the environment. The prefered substrates are linear secondary-alkyl sulfate esters, particularly octan-2-yl, octan-3-yl, and octan-4-yl sulfates. The enzyme from Pseudomonas sp. DSM6611 utilizes a range of secondary-alkyl sulfate esters bearing aromatic, olefinic and acetylenic moieties. Perfect enantioselectivities are obtained for substrates bearing groups of different size adjacent to the sulfate moiety. The enzymic hydrolysis proceeds through inversion of the configuration at the stereogenic carbon atom. The enzyme contains a Zn2+ ion. Group: Enzymes. Synonyms: S3 secondary alkylsulphohydrolase; Pisa1; secondary alkylsulphohydrolase; (R)-specific sec-alkylsulfatase; sec-alkylsulfatase. Enzyme Commission Number: EC 3.1.6.19. 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-3752; (R)-specific secondary-alkylsulfatase; EC 3.1.6.19; S3 secondary alkylsulphohydrolase; Pisa1; secondary alkylsulphohydrolase; (R)-specific sec-alkylsulfatase; sec-alkylsulfatase. Cat No: EXWM-3752. | |
| Samarium Sulfide | Samarium Sulfide is a moderately water and acid soluble Samarium source for uses compatible with sulfates. Uses: Designed for use in research and industrial production. Additional or Alternative Names: SAMARIUM SULFIDE;disamarium trisulphide;SAMARIUM SULFIDE 99.9%. Product Category: Heterocyclic Organic Compound. Appearance: red-brown crystals. CAS No. 12067-22-0. Molecular formula: Sm2S3. Mole weight: 397g/mol. Purity: 0.96. IUPACName: samarium(3+) trisulfide. Canonical SMILES: [S-2].[S-2].[S-2].[Sm+3].[Sm+3]. Density: 5.87g/mL. ECNumber: 235-076-6. Product ID: ACM12067220. Alfa Chemistry ISO 9001:2015 Certified. | |
| Scandium Sulfide | Scandium Sulfide is a moderately water and acid soluble Scandium source for uses compatible with sulfates. Sulfate compounds are salts or esters of sulfuric acid formed by replacing one or both of the hydrogens with a metal. Most metal sulfate compounds are readily soluble in water for uses such as water treatment, unlike fluorides and oxides which tend to be insoluble. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Scandium sulfide, Discandium trisulphide, Scandium sulfide (Sc2S3), EINECS 235-320-1, CID166646, 12166-29-9. Product Category: Heterocyclic Organic Compound. Appearance: yellow crystals. CAS No. 12166-29-9. Molecular formula: Sc2S3. Mole weight: 186g/mol. Purity: 0.96. IUPACName: scandium(3+) trisulfide. Density: 2.91g/mL. Product ID: ACM12166299. Alfa Chemistry ISO 9001:2015 Certified. | |
| SLES | SLES is an anionic surfactant which is widely used in rinse off products as a primary surfactant. In addition to excellent detergency (also referred as cleansing), it also has excellent emulsification and foamability. It is major component of rinse-off products. It is compatible with all surfactants except cationic. Uses: Detergents: SLES is a key ingredient in the production of laundry detergents, dishwashing liquids, and other cleaning agents. It helps to remove dirt, grease, and stains from surfaces and fabrics.Personal care products: SLES is used as a surfactant in the production of personal care products such as shampoos, body washes, and shower gels. It helps to create a lather and cleanse the skin and hair.Oil and gas industry: SLESis used in the oil and gas industry as a drilling and fracturing fluid, as well as a gelling agent in the production of drilling muds.Industrial cleaning: SLES is used as a cleaning agent in a variety of industrial applications, including in the production of paints, inks, and other coatings.Other uses: SLES may also be used in the production of emulsifiers, wetting agents, and other chemical intermediates. Group: surfactant. Alternative Names: (Alcohols, C12-14, ethoxylated, sulfates, sodium salts;) (Linear C12-14-alkanol, ethoxylated, sulfated, sodium salt;) SLES 70%; SLES 70% 2EO; SLES 70% 3EO; Sodium Laureth Sulfate. CAS No. 9004-82-4. Pack Sizes: 200 KG / HDPE Drums Packing. |  |
| steryl-sulfatase | Also acts on some related steryl sulfates. Group: Enzymes. Synonyms: arylsulfatase; steroid sulfatase; sterol sulfatase; dehydroepiandrosterone sulfate sulfatase; arylsulfatase C; steroid 3-sulfatase; steroid sulfate sulfohydrolase; dehydroepiandrosterone sulfatase; pregnenolone sulfatase; phenolic steroid sulfatase; 3-β-hydroxysteroid sulfate sulfatase. Enzyme Commission Number: EC 3.1.6.2. CAS No. 9025-62-1. 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-3753; steryl-sulfatase; EC 3.1.6.2; 9025-62-1; arylsulfatase; steroid sulfatase; sterol sulfatase; dehydroepiandrosterone sulfate sulfatase; arylsulfatase C; steroid 3-sulfatase; steroid sulfate sulfohydrolase; dehydroepiandrosterone sulfatase; pregnenolone sulfatase; phenolic steroid sulfatase; 3-β-hydroxysteroid sulfate sulfatase. Cat No: EXWM-3753. | |
| Sulfuric acid,titanium(3+) salt (3:2) | Sulfuric acid,titanium(3+) salt (3:2). Uses: Designed for use in research and industrial production. Additional or Alternative Names: dititaniumtris(sulphate); Titanoussulfatesolution; TITANIUM SULFATE; Sulfuric acid,titaniumsalt; Titanoussulphate; TITANIUM (III) SULFA; Titanous sulphate,solution; titanium sesquisulfate. Product Category: Heterocyclic Organic Compound. CAS No. 10343-61-0. Molecular formula: H2O4 S. 2/3 Ti. Mole weight: 383.92. Purity: 0.96. IUPACName: titanium(3+) trisulfate. Canonical SMILES: [O-]S(=O)(=O)[O-].[O-]S(=O)(=O)[O-].[O-]S(=O)(=O)[O-].[Ti+3].[Ti+3]. Density: 1.456 g/mL at 25ºC. ECNumber: 233-749-9. Product ID: ACM10343610. Alfa Chemistry ISO 9001:2015 Certified. | |
| Thulium Sulfide | Thulium Sulfide is a moderately water and acid soluble Thulium source for uses compatible with sulfates. Sulfate compounds are salts or esters of sulfuric acid formed by replacing one or both of the hydrogens with a metal. Uses: Designed for use in research and industrial production. Additional or Alternative Names: THULIUM SULFIDE;dithulium trisulphide;THULIUM SULFIDE, 99.99%;thuliumsulfide99.9%;Thulium (III) sulfide, 99.9% (REO). Product Category: Heterocyclic Organic Compound. Appearance: Powder. CAS No. 12166-30-2. Molecular formula: Tm2S3. Mole weight: 434g/mol. Product ID: ACM12166302. Alfa Chemistry ISO 9001:2015 Certified. | |
| xylosylprotein 4-β-galactosyltransferase | Involved in the biosynthesis of the linkage region of glycosaminoglycan chains as part of proteoglycan biosynthesis (chondroitin, dermatan and heparan sulfates). Requires Mn2+. Group: Enzymes. Synonyms: UDP-D-galactose:D-xylose galactosyltransferase; UDP-D-galactose:xylose galactosyltransferase; galactosyltransferase I; uridine diphosphogalactose-xylose galactosyltransferase; UDP-galactose:O-β-D-xylosylprotein 4-β-D-galactosyltransferase; UDP-α-D-galactose:O-β-D-xylosylprotein 4-β-D-galactosyltransferase; UDP-α-D-galactose:O-β-D-xylosyl-[protein] 4-β-D-galactosyltransferase. Enzyme Commission Number: EC 2.4.1.133. CAS No. 52227-72-2. 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-2358; xylosylprotein 4-β-galactosyltransferase; EC 2.4.1.133; 52227-72-2; UDP-D-galactose:D-xylose galactosyltransferase; UDP-D-galactose:xylose galactosyltransferase; galactosyltransferase I; uridine diphosphogalactose-xylose galactosyltransferase; UDP-galactose:O-β-D-xylosylprotein 4-β-D-galactosyltransferase; UDP-α-D-galactose:O-β-D-xylosylprotein 4-β-D-galactosyltransferase; UDP-α-D-galactose:O-β-D-xylosyl-[protein] 4-β-D-galactosyltransferase. Cat No: EXWM-2358. | |
| Ytterbium atomic absorption standard solution | Ytterbium atomic absorption standard solution. Uses: Thulium sulfate octahydrate, also called thulium sulphate, has specialized uses in ceramics, glass, phosphors, lasers, also is the important dopant for fibre amplifiers. thulium sulfate is a moderately water and acid soluble thulium source for uses compatible with sulfates. sulfate compounds are salts or esters of sulfuric acid formed by replacing one or both of the hydrogens with a metal. Group: Reference-calibration standards. | |
| Ytterbium(III) acetate tetrahydrate | Ytterbium(III) acetate tetrahydrate. Uses: Thulium sulfate octahydrate, also called thulium sulphate, has specialized uses in ceramics, glass, phosphors, lasers, also is the important dopant for fibre amplifiers. thulium sulfate is a moderately water and acid soluble thulium source for uses compatible with sulfates. sulfate compounds are salts or esters of sulfuric acid formed by replacing one or both of the hydrogens with a metal. Group: Solution deposition precursors. Alternative Names: KS-00000ETU; ytterbium(iII)acetate hydrate; 7722AF; C6H9O6Yb.4H2O; K-4840; 15280-58-7; Ytterbium(III) acetate hydrate. CAS No. 15280-58-7. Product ID: acetic acid; ytterbium; tetrahydrate. Molecular formula: 425.27g/mol. Mole weight: C6H20O10Yb. CC(=O)O. CC(=O)O. CC(=O)O. O. O. O. O. [Yb]. InChI=1S/3C2H4O2.4H2O.Yb/c3*1-2(3)4; ; ; ; ; /h3*1H3, (H, 3, 4); 4*1H2;. QBNWQWZCQVJAAD-UHFFFAOYSA-N. | |
| [1,1'-Biphenyl]-4-yl(1-trityl-1H-imidazol-5-yl)methanone | [1,1'-Biphenyl]-4-yl(1-trityl-1H-imidazol-5-yl)methanone is an intermediate in synthesizing 2-Biphenylyl Sulfate-d5 Potassium Salt (B397897), which is the isotope labelled analog of 2-Biphenylyl Sulfate Potassium Salt. 2-Biphenylyl Sulfate Potassium Salt is a derivative of 2-Phenylphenol (P335870). 2-Phenylphenol is a agriculture fungicide and is no longer used as a food additive. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 25mg, 50mg. Molecular Formula: C35H26N2O. US Biological Life Sciences. | Worldwide |
| [1,1'-Biphenyl]-4-yl(phenyl)(1-trityl-1H-imidazol-5-yl)methanol | [1,1'-Biphenyl]-4-yl(phenyl)(1-trityl-1H-imidazol-5-yl)methanol is an intermediate in synthesizing 2-Biphenylyl Sulfate-d5 Potassium Salt (B397897), which is the isotope labelled analog of 2-Biphenylyl Sulfate Potassium Salt. 2-Biphenylyl Sulfate Potassium Salt is a derivative of 2-Phenylphenol (P335870). 2-Phenylphenol is a agriculture fungicide and is no longer used as a food additive. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg, 25mg. Molecular Formula: C41H32N2O. US Biological Life Sciences. | Worldwide |
| 1,1-Diethylguanidine sulfate | 1,1-Diethylguanidine sulfate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1,1-DIETHYLGUANIDINE SULFATE;N,N-DIETHYLGUANIDINE SULFATE (2:1);N,N-diethylguanidinium sulphate (2:1);2(1,1-Diethylguanidine)·sulfuric acid. Product Category: Heterocyclic Organic Compound. CAS No. 77297-00-8. Molecular formula: C10H28N6O4S. Mole weight: 328.43. Product ID: ACM77297008. Alfa Chemistry ISO 9001:2015 Certified. Categories: 54259-07-3. | |
| 1,1-Dimethyl guanidinium sulfate | 1,1-Dimethyl guanidinium sulfate. Group: Biochemicals. Grades: Highly Purified. CAS No. 598-65-2,1186-46-5. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C3H9N3·½H2SO4. US Biological Life Sciences. | Worldwide |
| 1,2,3-trimethylimidazolium methylsulfate | 1,2,3-trimethylimidazolium methylsulfate. Uses: Metal plating, electropolishing, metal reprocessing, phase transfer media, batteries fuel cells, nanomaterials, industrial solvents, nuclear fuel red waste, enzymatic catalysis, lubricants heat transfer and solar energy conversion. Group: Electrolytes. CAS No. 65086-12-6. Product ID: methyl sulfate; 1,2,3-trimethylimidazol-1-ium. Molecular formula: 222.26. Mole weight: C7H14N2O4S. CC1=[N+](C=CN1C)C.COS(=O)(=O)[O-]. InChI=1S/C6H11N2. CH4O4S/c1-6-7(2)4-5-8(6)3; 1-5-6(2, 3)4/h4-5H, 1-3H3; 1H3, (H, 2, 3, 4)/q+1; /p-1. OUAUEIYYLHUEPK-UHFFFAOYSA-M. 98% min. | |
| 1,2,5,6-Tetrahydro-4H-pyrrolo[3,2,1-ij]quinolin-8-amine sulfate | 1,2,5,6-Tetrahydro-4H-pyrrolo[3,2,1-ij]quinolin-8-amine sulfate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Lilolidine,8-amino-,sulfate (2:1) (crude); 1,2,5,6-Tetrahydro-8-amino-4H-pyrrolo(3,2,1-ij)quinoline sulfate (2:1) (crude); 1,2,5,6-Tetrahydro-4H-pyrrolo[3,2,1-ij]chinolin-8-ylamin,Sulfat; 4H-Pyrrolo(3,2,1-ij)quinoline,1,2,5,6-tetrahydro-8-amino-,sulfate (. Product Category: Heterocyclic Organic Compound. CAS No. 102280-97-7. Molecular formula: C22H30N4O4S. Mole weight: 446.56. Purity: 0.96. IUPACName: 8-Aminolilolidine 1/2 hydrosulfate (crude). Product ID: ACM102280977. Alfa Chemistry ISO 9001:2015 Certified. Categories: DB-225864. | |
| 12-Hydroxy Taurolithocholic Acid-2,2,3,4,4-d5 Sulfate Disodium Salt | 12-Hydroxy Taurolithocholic Acid-2,2,3,4,4-d5 Sulfate Disodium Salt is a laballed analogue of 2-Hydroxy Taurolithocholic Acid Sulfate Disodium Salt (H954090), an impurity of Cholic Acid (C432600), which is a choleretic produced by and isolated from liver cells. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug, 1mg. Molecular Formula: C26H38D5NNa2O9S2, Molecular Weight: 628.76. US Biological Life Sciences. | Worldwide |
| 12-Hydroxy Taurolithocholic Acid Sulfate Disodium Salt | 2-Hydroxy Taurolithocholic Acid Sulfate Disodium Salt is an impurity of Cholic Acid (C432600), a choleretic produced by and isolated from liver cells. Group: Biochemicals. Grades: Highly Purified. CAS No. 66874-07-5. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C26H43NNa2O9S2. US Biological Life Sciences. | Worldwide |
| 1-? (2-?Mercaptoethyl) ?guanidine Sulfate | MEG (sulfate) is a selective NOS2 inhibitor. MEG protects against plasma extravasation and bone destruction. Group: Biochemicals. Grades: Highly Purified. CAS No. 3979-00-8. Pack Sizes: 5mg, 10mg. Molecular Formula: C6H20N6O4S3, Molecular Weight: 336.46. US Biological Life Sciences. | Worldwide |
| 1-(2-Sulfosulfanylethylamino)decane | 1-(2-Sulfosulfanylethylamino)decane. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-n-Decylamino-ethanthioschwefelsaeure; 2-Decylamino-aethyl-thioschwefelsaeure; s-[2-(decylamino)ethyl] hydrogen sulfurothioate; 2-(n-Decylamino)-ethanethiosulfuric acid; Ethanethiol,2-decylamino-,hydrogen sulfate (ester); 2-(1-Decylamino)ethanethiosulfur. Product Category: Heterocyclic Organic Compound. CAS No. 3752-51-0. Molecular formula: C12H27NO3S2. Mole weight: 297.478 g/mol. Purity: 0.96. IUPACName: 1-(2-sulfosulfanylethylamino)decane. Canonical SMILES: CCCCCCCCCCNCCSS(=O)(=O)O. Density: 1.11g/cm³. Product ID: ACM3752510. Alfa Chemistry ISO 9001:2015 Certified. | |
| 1-(2-Sulfosulfanylethylamino)pentadecane | 1-(2-Sulfosulfanylethylamino)pentadecane. Group: other materials. Alternative Names: 2-Pentadecylaminoethanethiol hydrogen sulfate (ester), s-[2-(pentadecylamino)ethyl] hydrogen sulfurothioate, WR 2345, BRN 2380996, Thiosulfuric acid, S-(2-(pentadecylamino)ethyl) ester, Ethanethiol, 2-pentadecylamino-, hydrogen sulfate (ester), 929-44-2, AC1L2DNN, AC1Q6XQE, AR-1L3693, 1-(2-sulfosulfanylethylamino)pentadecane, LS-66059. CAS No. 92-94-4. Product ID: 1-(2-sulfosulfanylethylamino)pentadecane. Molecular formula: 367.611 g/mol. Mole weight: C17< / sub>H37< / sub>NO3< / sub>S2< / sub>. CCCCCCCCCCCCCCCNCCSS(=O)(=O)O. KUDPDOZAPFSKPG-UHFFFAOYSA-N. 96%. | |
| 1,3,2-Dioxathiane 2,2-Dioxide | 1,3,2-Dioxathiane 2,2-Dioxide. Group: Biochemicals. Alternative Names: 1,3-Propanediol Cyclic Sulfate; 1,3-Propylene Sulfate; Trimethylene Sulfate. Grades: Highly Purified. CAS No. 1073-05-8. Pack Sizes: 10g, 25g, 50g, 100g, 250g. US Biological Life Sciences. | Worldwide |
| 1,3,2-Dioxathiolane 2,2-Dioxide | 1,3,2-Dioxathiolane 2,2-Dioxide. Group: Battery materials. Alternative Names: Ethylene Sulfate. CAS No. 1072-53-3. Product ID: 1,3,2-dioxathiolane 2,2-dioxide. Molecular formula: 124.11. Mole weight: C2H4O4S. C1COS(=O)(=O)O1. InChI=1S/C2H4O4S/c3-7 (4)5-1-2-6-7/h1-2H2. ZPFAVCIQZKRBGF-UHFFFAOYSA-N. >98.0%(GC). | |
| 1,3,2-Dioxathiolane 2,2-Dioxide | 1,3,2-Dioxathiolane 2,2-Dioxide is an alkylating agent with carcinogenic activty. Group: Biochemicals. Alternative Names: Ethylene Glycol Cyclic Sulfate; 1,2-Ethylene Sulfate; Ethylene Sulfate; NSC 526594. Grades: Highly Purified. CAS No. 1072-53-3. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| 1,3,5(10),6,8-Estrapentaen-3-ol-17-one sulphate,sodium salt | 1,3,5(10),6,8-Estrapentaen-3-ol-17-one sulphate,sodium salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: EQUILENIN SODIUM SULFATE;EQUILENIN SODIUM SULPHATE;1,3,5(10)-6,8-ESTRAPENTAEN-3-OL-17-ONE 3-SULFATE SODIUM;1,3,5(10), 6,8-ESTRAPENTAEN-3-OL-17-ONE SULPHATE, SODIUM SALT;Estra-1,3,5,7,9-pentaen-17-one, 3-(sulfooxy)-, sodium salt;3-(Sodiosulfooxy)-1,3,5,7. Product Category: Heterocyclic Organic Compound. CAS No. 16680-48-1. Molecular formula: C18H17NaO5S. Mole weight: 368.38. Product ID: ACM16680481. Alfa Chemistry ISO 9001:2015 Certified. Categories: Sodium equilenin sulfate. | |
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