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| Product | Description | |
|---|---|---|
| Chitin | . also available in pharma grade. CAS No. 1398-61-4. Product ID: 4-00020. |  |
| Chitin | Chitin. Group: Molecular Biology. CAS No. 1398-61-4. Pack Sizes: 25g, 250g. Molecular Formula: C30H50N4O19. US Biological Life Sciences. |  Worldwide |
| Chitin | Chitin. Synonyms: Poly-(1→4)-β-N-acetyl-D-glucosamine. CAS No. 1398-61-4. Pack Sizes: 100 g, 1 kg. Product ID: CDC10-0010. Molecular formula: C8H15NO6. Category: Cosmetic Chemical Abrasives. Product Keywords: Cosmetic Ingredients; Cosmetic Chemical Abrasives; Chitin; CDC10-0010; 1398-61-4; C8H15NO6; Poly-(1→4)-β-N-acetyl-D-glucosamine; 215-744-3; MFCD00466914; 1398-61-4. Grade: practical grade. EC Number: 215-744-3. Physical State: Powder. Solubility: Dilute aqueous acid (pH <6.5).: soluble. Quality Level: 200. Boiling Point: 522.4ºC at 760 mmHg. Melting Point:>300°C (dec.). Density: 1.37 g/cm3. |  |
| Chitin | Chitin. We stock inventory in warehouses throughout the United States, allowing us to serve customers in all regions in a timely and cost effective manner. |  California |
| Chitin | It is produced by the strain of Fungi, yeasts, Marine vertebrates and arthropods. Chitin is often used as a trauma therapy and its product of the Chitosan can be used for water treatment and the preparation of photographic emulsion fluid. Uses: Occurs naturally in fungi, yeasts, marine invertebrates, and exoskeletons of arthropods; the second most abundant biopolymer on earth; used to make chitosan; used to control nematodes in various field crops, ornamentals, turf grown in fields, home gardens, and nurseries. Synonyms: Poly-(b1-4)-N-acetyl glucosamine; Poly-(a1-4)-N-acetyl glucosamine. CAS No. 1398-61-4. Molecular formula: (C8H13NO5)n. |  |
| Chitin | Poly(N-Acetylglucosamine). from crab shells. Grades: High purity powder. CAS No. 1398-61-4. Product ID: 4-00019. Properties: flakes, technical. Source : from crab shells. | |
| Chitin | The monomers are identified as N-Acetyl-Amnioglucose. Chitin is a polysaccharide containing nitrogen in which monomers occur with the glycosidically linked components beta 1,4. It is the same coupling as glucose with cellulose, however in chitin the hydroxyl group of the monomer is replaced with an acetyl amine group. The resulting, stronger hydrogen bond between the bordering polymers makes chitin harder and more stabile than cellulose. Group: Polymers. Alternative Names: (1,4)-N-acetyl-D-glucos-2-amine. CAS No. 1398-61-4. Pack Sizes: 1 ton. Product ID: N-[(2R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide. Molecular formula: 161.16. Mole weight: (C8H13NO5)n. CC(=O)NC1[C@@H](OC(C(C1O)O)CO)O. OVRNDRQMDRJTHS-WTZNIHQSSA-N. InChI=1S/C8H15NO6/c1-3 (11)9-5-7 (13)6 (12)4 (2-10)15-8 (5)14/h4-8, 10, 12-14H, 2H2, 1H3, (H, 9, 11)/t4?, 5?, 6?, 7?, 8-/m1/s1. 96%. |  |
| chitinase | Some chitinases also display the activity defined in EC 3.2.1.17 lysozyme. Group: Enzymes. Synonyms: chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase. Enzyme Commission Number: EC 3.2.1.14. CAS No. 9001-6-3. Chitinase. 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-3822; chitinase; EC 3.2.1.14; 9001-06-3; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase. Cat No: EXWM-3822. |  |
| CHITINASE | HGAPDH is an antifungal peptide isolated from Streptomyces violaceus. Synonyms: Glu-Gln-Pro-Gly-Gly-Asp-Lys-Val-Asn-Leu-Gly-Tyr-Phe-Thr-Asn. Grades: 96.9%. CAS No. 9001-6-3. Molecular formula: C72H107N19O25. Mole weight: 1638.75. | |
| Chitinase 18A from Bacillus cereus, Recombinant | Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.14. Purity: >90% by SDS-PAGE. Chitosanase. Mole weight: 38.3 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus cereus. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase; Chitosanase 18A. Cat No: NATE-1377. | |
| Chitinase 18A from Bacillus licheniformis, Recombinant | Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.14. Purity: >90% by SDS-PAGE. Chitosanase. Mole weight: 49.2 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus licheniformis. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase; Chitosanase 18A. Cat No: NATE-1378. | |
| Chitinase 18A from Clostridium thermocellum, Recombinant | Chitosanase catalyzes the endohydrolysis of β (1,4) linkages between N-acetyl-D-glucosamine and D-glucosamine residues in partially deacetylated chitosan. Chitosanase from Streptomyces griseus is capable of hydrolyzing both chitosan and carboxymethyl cellulose. It is used for the lysis of cell walls of fungi belonging to the group Mucorales. It is found in several types of microorganisms. Group: Enzymes. Synonyms: Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase. Enzyme Commission Number: EC 3.2.1.14. Purity: >90% by SDS-PAGE. Chitosanase. Mole weight: 43.9 kDa. Activity: 25 U/mg. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Clostridium thermocellum. Chitosanase; EC 3.2.1.132; 51570-20-8; Chitosan N-acetylglucosaminohydrolase; Chitosanase 18A. Cat No: NATE-1379. | |
| Chitinase from Aspergillus niger (food grade) | Chitinase is an extracellular enzyme complex that degrades chitin. Chitin is degraded to N-acetyl-D-glucosamine in 2 enzymatic reactions. Group: Enzymes. Synonyms: Chitinase; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Enzyme Commission Number: EC 3.2.1.14. CAS No. 9001-6-3. Chitinase. Activity: 200U/g min. Stability: 1 year when properly stored. Storage: STORED HUMIDITY PROTECTED (RH LESS THAN 60) AT TEMPERATURE BELOW 25°C. Form: Light-brown Powder. Source: Aspergillus niger. Chitinase; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Cat No: DIS-1010. | |
| Chitinase from Clostridium thermocellum, Recombinant | Chitinase is an extracellular enzyme complex that degrades chitin and has a molecular mass of approximately 30 kDa. Chitin is degraded to N-acetyl-D-glucosamine in 2 enzymatic reactions. Firstly, chitobiose units are removed from chitin by chitodextrinase-chitinase. The second reaction involves N-acetyl-glucosaminidase-chitobiase, which cleaves the disaccharide to its monomer subunits (that comprise of N-acetyl-D-glucosamine). Group: Enzymes. Synonyms: Chitinase; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Enzyme Commission Number: EC 3.2.1.14. Purity: > 80 % as judged by SDS-PAGE. Chitinase. Mole weight: 43927.1 Da. Activity: 25 U/mg. Storage: Store at -20°C (shipped at room temperature). Form: Glycerol/buffer solution. Source: Clostridium thermocellum ATCC 27405. Chitinase; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Cat No: NATE-1201. | |
| Chitinase-IN-1 | Chitinase-IN-1 is a insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide; 50 uM/20uM compound concentration's inhibitory percentage are 75%/67% for chitinase/N- acetyl-hexosaminidase respectively. Synonyms: Chitinase-IN-1. Grades: >98%. CAS No. 1579991-61-9. Molecular formula: C18H16N4O2S. Mole weight: 352.41. | |
| Chitinase-IN-2 | Chitinase-IN-2 is a insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide; 50 uM/20uM compound concentration's inhibitory percentage are 98%/92% for chitinase/N- acetyl-hexosaminidase respectively. Synonyms: Chitinase-IN-2. Grades: >98%. CAS No. 1579991-63-1. Molecular formula: C20H21N5O2S. Mole weight: 395.48. | |
| Chitinase, Serratia marcescens | Chitinase, Serratia marcescens (EC 3.2.1.14) has partial lysozyme activity and is widely found in bacteria, fungi, animals and some plants. Chitinase belongs to the glycosyl hydrolase family. Chitinase catalyzes chito-oligosaccharide hydrolysis. Chitinases also can serve as prognostic biomarkers of disease progression. Chitinase can be used in the research of pathogenesis of various human fibrotic and inflammatory disorders, particularly those of the lung (idiopathic pulmonary fibrosis, chronic obstructive pulmonary disease, sarcoidosis, and asthma) and the gastrointestinal tract (inflammatory bowel diseases (IBDs) and colon cancer) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AMCase, Serratia marcescens. CAS No. 9001-6-3. Pack Sizes: 5 U. Product ID: HY-P2797. |  |
| Chitinase, Streptomyces griseus | Chitinase, Streptomyces griseus is a chitinase mainly found in Bacillus species and uses colloidal chitin as a substrate. The Km and Vmax of Chitinase are 4.28 mg/mL and 14.29 μg/(Min·mL) respectively. The final enzymatic hydrolysis product is N-acetylglucosamine, and the monomer and dimer contents are 14.33% and 85.67% respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AMCase, Streptomyces griseus. CAS No. 9001-6-3. Pack Sizes: 1 g; 5 g. Product ID: HY-P2797A. | |
| Chitin azure | Chitin azure. Group: Natural polymers and biopolymers. | |
| Chitin azure | Chitin azure has been used as a substrate to determine chitinase activity. | |
| Chitin Azure | suitable for determining polygalacturonase activity. Product ID: 9-01082. Purity: 'dye content ~5-7 mol%. Properties: Reference: J Biol Chem.,,279, 21888, 2004; Cancer Res., 54, 4516, 1994. | |
| Chitin-binding protein 3 | Chitin-binding protein 3 is an antifungal peptide isolated from Moringa oleifera. It has activity against gram-negative bacteria and fungi. Synonyms: Mo-CBP3; Cys-Pro-Ala-Ile-Gln-Arg-Cys-Cys-Gln-Gln-Leu-Arg-Asn-Ile-Gln-Pro-Pro-Cys-Arg-Cys-Cys-Gln. | |
| chitin deacetylase | Hydrolyses the N-acetamido groups of N-acetyl-D-glucosamine residues in chitin. Group: Enzymes. Enzyme Commission Number: EC 3.5.1.41. CAS No. 56379-60-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4430; chitin deacetylase; EC 3.5.1.41; 56379-60-3. Cat No: EXWM-4430. | |
| chitin disaccharide deacetylase | Chitin oligosaccharide deacetylase is a key enzyme in the chitin catabolic cascade of chitinolytic Vibrio strains. Besides being a nutrient, the heterodisaccharide product 4-O-(N-acetyl-β-D-glucosaminyl)-D-glucosamine is a unique inducer of chitinase production in Vibrio parahemolyticus. In contrast to EC 3.5.1.41 (chitin deacetylase) this enzyme is specific for the chitin disaccharide. It also deacetylates the chitin trisaccharide with lower efficiency. No activity with higher polymers of GlcNAc. Group: Enzymes. Synonyms: chitobiose amidohydolase; COD; chitin oligosaccharide deacetylase; chitin oligosaccharide amidohydolase; 2-(acetylamino)-4-O-[2-(acetylamino)-2-deoxy-β-D-glucopyranosyl]-2-deoxy-D-glucopyranose acetylhydrolase. Enzyme Commission Number: EC 3.5.1.105. 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-4384; chitin disaccharide deacetylase; EC 3.5.1.105; chitobiose amidohydolase; COD; chitin oligosaccharide deacetylase; chitin oligosaccharide amidohydolase; 2-(acetylamino)-4-O-[2-(acetylamino)-2-deoxy-β-D-glucopyranosyl]-2-deoxy-D-glucopyranose acetylhydrolase. Cat No: EXWM-4384. | |
| Chitin, ethylene glycol | also available in pharma grade. CAS No. 9056-32-0. Product ID: 4-00021. Properties: granule size <0.2 mm. Source : from crab shells. | |
| Chitin from shrimp shells | Chitin from shrimp shells. Group: Natural polymers and biopolymerspolysaccharide. Alternative Names: (1,4)-N-acetyl-D-glucos-2-amine. CAS No. 1398-61-4. CC (=O)N[C@@H]1[C@H] (O)O[C@@H] (CO)[C@H] (O)[C@H]1O. 1S/C8H15NO6/c1-3 (11)9-5-7 (13)6 (12)4 (2-10)15-8 (5)14/h4-8, 10, 12-14H, 2H2, 1H3, (H, 9, 11)/t4?, 5?, 6?, 7?, 8-/m1/s1. OVRNDRQMDRJTHS-WTZNIHQSSA-N. | |
| Chitin Nanoparticles | Chitin Nanoparticles. Group: Clay nanopowders. CAS No. 1398-61-4. Molecular formula: 770.8g/mol. Mole weight: C30H50N4O19. >99%. | |
| Chitin Oligosaccharides | Chitin Oligosaccharides. CAS No. 1398-61-4. Product ID: 4-00647. | |
| Chitinovorin A | Chitinovorin A is produced by the strain of Flavobacerium chitinovorum PB-5016 and PB-5246. Molecular formula: C26H41N9O11S. Mole weight: 687.73. | |
| Chitinovorin B | Chitinovorin B is produced by the strain of Flavobacerium chitinovorum PB-5016 and PB-5246. Synonyms: L-Alaninamide, L-alanyl-N-(4-((7-((5-amino-5-carboxy-1-oxopentyl)amino)-2-carboxy-7-(formylamino)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-en-3-yl)methoxy)-1-(3-((aminoiminomethyl)amino)propyl)-2-hydroxy-4-oxobutyl)-, (6R-(3(1S*,2R*),6alpha,7beta(R*)))-. Grades: >98%. CAS No. 95722-76-2. Molecular formula: C29H46N10O12S. Mole weight: 758.80. | |
| Chitinovorin C | Chitinovorin C is produced by the strain of Flavobacerium chitinovorum PB-5016 and PB-5246. It has weak anti-gram-negative bacterial activity. Synonyms: 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 7-((5-amino-5-carboxy-1-oxopentyl)amino)-7-(formylamino)-3-(hydroxymethyl)-8-oxo-, (6R-(6alpha,7beta(R*)))-; 7-[(5-Amino-5-carboxy-1-hydroxypentylidene)amino]-3-(hydroxymethyl)-7-[(hydroxymethylidene)amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. CAS No. 95230-98-1. Molecular formula: C15H20N4O8S. Mole weight: 416.41. | |
| Chitin phosphate | Chitin phosphate. Product ID: 5-02283. Purity: highly phosphorylated chitin (P 5-7%). Properties: water insoluble. | |
| Chitin phosphate sulphate | phosphorylated and sulfated chitin. Product ID: 5-02284. Properties: Water soluble, salt free sulfated with potential biological activity. | |
| Chitin sulphate | Chitin sulphate. Product ID: 5-02537. Properties: Water soluble, salt free anionic polysaccharide with potential biological activity. | |
| chitin synthase | Converts UDP-N-acetyl-α-D-glucosamine into chitin and UDP. Group: Enzymes. Synonyms: chitin-UDP N-acetylglucosaminyltransferase; chitin-uridine diphosphate acetylglucosaminyltransferase; chitin synthetase; trans-N-acetylglucosaminosylase; UDP-N-acetyl-D-glucosamine:chitin 4-β-N-acetylglucosaminyl-transferase. Enzyme Commission Number: EC 2.4.1.16. CAS No. 9030-18-6. 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-2384; chitin synthase; EC 2.4.1.16; 9030-18-6; chitin-UDP N-acetylglucosaminyltransferase; chitin-uridine diphosphate acetylglucosaminyltransferase; chitin synthetase; trans-N-acetylglucosaminosylase; UDP-N-acetyl-D-glucosamine:chitin 4-β-N-acetylglucosaminyl-transferase. Cat No: EXWM-2384. | |
| 6-O-Carboxymethyl chitin | 6O-CMC. Product ID: 5-00934. Purity: Purified powder water soluble, salt free. Properties: prevents postsurgical adhesion. | |
| 6-O-Oxychitin | Oxidized chitin. biodegradable anti-scaling agent. Product ID: 5-02531. Purity: purified powder water soluble, salt free. | |
| Acidic Mammalian Chitinase Inhibitor, Bisdionin F | A cell-permeable, competitive Acidic Mammalian Chitinase (AMCase) Inhibitor (IC50=0.92uM and Ki=0.42uM for hAMCase, and IC50=2.2uM for mAMCase, in vitro) that demonstrates 20-fold selectivity for hAMCase over hCHIT1. It is shown to decrease chitinase enzymatic activity (5mg/kg, i.p.) in the lungs of control PBS- and OVA-challenged mice. Furthermore, it attenuates lung chitinase activity, reduces eosinophil influx, and improves ventilatory function, in vivo, in a murine model of allergic inflammation. It also causes neutrophilia in the lungs of OVA-challenged mice. Group: Biochemicals. Alternative Names: AMCase Inhibitor, 3,7-dimethyl-1-(3-(3-methyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-1-yl)propyl)-1H-purine-2,6(3H,7H)-dione. Grades: Highly Purified. CAS No. 917877-86-2. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Ethylene Glycol Chitin | Ethylene Glycol Chitin. Uses: Designed for use in research and industrial production. Appearance: Lyophilisate. CAS No. 9056-32-0. Purity: 0.95. Product ID: ACM9056320. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Lytic chitin monooxygenase from Bacillus licheniformis, Recombinant | Lytic chitin monooxygenase is a copper-dependent lytic polysaccharide monooxygenase (LPMO). Copper-dependent lytic polysaccharide monooxygenases (LPMOs) are key players in the enzymatic conversion of biomass. LPMOs catalyze oxidative cleavage of glycosidic bonds in a process involving molecular oxygen and an electron donor, such as cellobiose dehydrogenase (CDH). Group: Enzymes. Synonyms: copper-dependent lytic polysaccharide monooxygenase; LPMO; lytic polysaccharide monooxygenase. Enzyme Commission Number: EC 1.-.-.-. Purity: >90% as judged by SDS-PAGE. Lytic polysaccharide monooxygenase. Mole weight: 21.2 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus licheniformis. copper-dependent lytic polysaccharide monooxygenase; LPMO; lytic polysaccharide monooxygenase. Cat No: NATE-1566. | |
| Lytic chitin monooxygenase from Lactococcus lactis, Recombinant | Lytic chitin monooxygenase is a copper-dependent lytic polysaccharide monooxygenase (LPMO). Copper-dependent lytic polysaccharide monooxygenases (LPMOs) are key players in the enzymatic conversion of biomass. LPMOs catalyze oxidative cleavage of glycosidic bonds in a process involving molecular oxygen and an electron donor, such as cellobiose dehydrogenase (CDH). Group: Enzymes. Synonyms: copper-dependent lytic polysaccharide monooxygenase; LPMO; lytic polysaccharide monooxygenase. Enzyme Commission Number: EC 1.-.-.-. Purity: >90% as judged by SDS-PAGE. Lytic polysaccharide monooxygenase. Mole weight: 21.8 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Lactococcus lactis. copper-dependent lytic polysaccharide monooxygenase; LPMO; lytic polysaccharide monooxygenase. Cat No: NATE-1567. | |
| Native Streptomyces griseus Chitinase | Chitinase is an extracellular enzyme complex that degrades chitin and has a molecular mass of approximately 30 kDa. Chitin is degraded to N-acetyl-D-glucosamine in 2 enzymatic reactions. Firstly, chitobiose units are removed from chitin by chitodextrinase-chitinase. The second reaction involves N-acetyl-glucosaminidase-chitobiase, which cleaves the disaccharide to its monomer subunits (that comprise of N-acetyl-D-glucosamine). Applications: Chitinase from streptomyces griseus has been used to study the effect of the allosamidin on the regulatory system for chitinase production. it has also been used to study the enrichment of chitinolytic microorganisms. this enrichment wa...;-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Enzyme Commission Number: EC 3.2.1.14. CAS No. 9001-6-3. Chitinase. Activity: > 200 units/g solid. Storage: -20°C. Form: lyophilized powder (essentially salt free). Source: Streptomyces griseus. Chitinase; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Cat No: NATE-0123. | |
| Native Trichoderma viride Chitinase | Chitinase is an extracellular enzyme complex that degrades chitin and has a molecular mass of approximately 30 kDa. Chitin is degraded to N-acetyl-D-glucosamine in 2 enzymatic reactions. Firstly, chitobiose units are removed from chitin by chitodextrinase-chitinase. The second reaction involves N-acetyl-glucosaminidase-chitobiase, which cleaves the disaccharide to its monomer subunits (that comprise of N-acetyl-D-glucosamine). Applications: Chitinase from trichoderma viride has been used in a study to investigate the differential release of high mannose structural isoforms by fungal and bacterial endo-β-n-acetylglucosaminidases. chitinase from trichoderma viride has al...glucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Enzyme Commission Number: EC 3.2.1.14. CAS No. 9001-6-3. Chitinase. Activity: > 600 units/g solid. Storage: -20°C. Form: lyophilized powder. Source: Trichoderma viride. Chitinase; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Cat No: NATE-0124. | |
| N,O-Ethylamine chitin | suitable for coupling to carboxyl- or aldehyde-containing ligands. Product ID: 5-00040. | |
| 1,3,4,6-Tetra-O-acetyl-2-[(2-aminoacetyl)amino]-2-deoxy-a-D-glucopyranose | 1,3,4,6-Tetra-O-acetyl-2-[(2-aminoacetyl)amino]-2-deoxy-a-D-glucopyranose, commonly referred to as TAAAG, serves as a vital chemical compound in the biomedical industry. Its application as a precursor to chitin synthesis inhibitors makes it an integral aspect of fungal infection and pest control treatment. The complex molecular structure of TAAAG has shown to impede chitin formation and thus, hinder fungal growth and pest development. Advanced research utilizing TAAAG has shown to provide exceptional results, making it an essential component for a myriad of biomedical applications. CAS No. 47577-85-5. Molecular formula: C16H24N2O10. Mole weight: 404.37. | |
| 1,3,4,6-Tetra-O-acetyl-2-tetrachlorophthalimide-2-deoxy-D-glucopyranose | 1,3,4,6-Tetra-O-acetyl-2-tetrachlorophthalimide-2-deoxy-D-glucopyranose is an intermediate formed in the synthesis of N-Acetylchitooctaose (A168460), a chitooligosaccharide used to activate Saccharomyces cerevisiae chitin biosynthesis. N-Acetylchitooctaose has affinity for NKR-P1A protein, the major activating receptor at the surface of rat natural killer (NK) cells, and may be useful in human therapy in cancer treatment (colon cancer, melanoma). Group: Biochemicals. Grades: Highly Purified. CAS No. 174356-26-4. Pack Sizes: 50mg, 100 mg. Molecular Formula: C22H19Cl4NO11, Molecular Weight: 615.2. US Biological Life Sciences. | Worldwide |
| 2,3,6-tri-O-Acetyl-2-tetrachlorophthalimide-1-benzenethiol-1,2-dideoxy- β-D-glucopyranose | 2,3,6-tri-O-Acetyl-2-tetrachlorophthalimide-1-benzenethiol-1,2-dideoxy- β-D-glucopyranose is an intermediate formed in the synthesis of N-Acetylchitooctaose (A168460), a chitooligosaccharide used to activate Saccharomyces cerevisiae chitin biosynthesis. N-Acetylchitooctaose has affinity for NKR-P1A protein, the major activating receptor at the surface of rat natural killer (NK) cells, and may be useful in human therapy in cancer treatment (colon cancer, melanoma). Group: Biochemicals. Grades: Highly Purified. CAS No. 217814-68-1. Pack Sizes: 25mg, 100mg. Molecular Formula: C26H21Cl4NO9S. US Biological Life Sciences. | Worldwide |
| 2,3,6-tri-O-Acetyl-2-tetrachlorophthalimide-1-benzenethiol-1,2-dideoxy-β-D-glucopyranose | 2,3,6-tri-O-Acetyl-2-tetrachlorophthalimide-1-benzenethiol-1,2-dideoxy-β-D-glucopyranose is an intermediate formed in the synthesis of N-Acetylchitooctaose, a chitooligosaccharide used to activate Saccharomyces cerevisiae chitin biosynthesis. N-Acetylchitooctaose has affinity for NKR-P1A protein, the major activating receptor at the surface of rat natural killer (NK) cells, and may be useful in human therapy in cancer treatment (colon cancer, melanoma). Synonyms: (2R,3S,4R,5R,6S)-2-(Acetoxymethyl)-6-(phenylthio)-5-(4,5,6,7-tetrachloro-1,3-dioxoisoindolin-2-yl)tetrahydro-2H-pyran-3,4-diyl Diacetate. CAS No. 217814-68-1. Molecular formula: C26H21Cl4NO9S. Mole weight: 665.32. | |
| 2-Iodopropane-d7 | 2-Iodopropane-d7 is the isotope labelled analog of 2-Iodopropane (I718795); a reagent used in the synthesis of 4'-O-alkyl-chitobiosyl-4-methylumbelliferone as human chitinase fluorogenic substrates. Group: Biochemicals. Grades: Highly Purified. CAS No. 101927-33-7. Pack Sizes: 10mg, 100 mg. Molecular Formula: C3D7I, Molecular Weight: 177. US Biological Life Sciences. | Worldwide |
| 2-Iodopropane (Stabilized with Copper) | 2-Iodopropane is used as a reagent in the synthesis of 4'-O-alkyl-chitobiosyl-4-methylumbelliferone as human chitinase fluorogenic substrates. Group: Biochemicals. Grades: Highly Purified. CAS No. 75-30-9. Pack Sizes: 1g, 10g. Molecular Formula: C3H7I. US Biological Life Sciences. | Worldwide |
| 3,6-O-diBenzyl-2-tetrachlorophthalimide-1-benzenethiol-1,2-dideoxy-β-D-glucopyranose | 3,6-O-diBenzyl-2-tetrachlorophthalimide-1-benzenethiol-1,2-dideoxy-β-D-glucopyranose is an intermediate formed in the synthesis of N-Acetylchitooctaose, a chitooligosaccharide used to activate Saccharomyces cerevisiae chitin biosynthesis. N-Acetylchitooctaose has affinity for NKR-P1A protein, the major activating receptor at the surface of rat natural killer (NK) cells, and may be useful in human therapy in cancer treatment (colon cancer, melanoma). Synonyms: 2-((2S,3R,4R,5S,6R)-4-(Benzyloxy)-6-((benzyloxy)methyl)-5-hydroxy-2-(phenylthio)tetrahydro-2H-pyran-3-yl)-4,5,6,7-tetrachloroisoindoline-1,3-dione. Molecular formula: C34H27Cl4NO6S. Mole weight: 719.46. | |
| 3,6-O-diBenzyl-4-O-tert-butyldimethylsilyl-2-tetrachlorophthalimide-1-benzenethiol-1,2-dideoxy-β-D-glucopyranose | 3,6-O-diBenzyl-4-O-tert-butyldimethylsilyl-2-tetrachlorophthalimide-1-benzenethiol-1,2-dideoxy-β-D-glucopyranose is an intermediate formed in the synthesis of N-Acetylchitooctaose, a chitooligosaccharide used to activate Saccharomyces cerevisiae chitin biosynthesis. N-Acetylchitooctaose has affinity for NKR-P1A protein, the major activating receptor at the surface of rat natural killer (NK) cells, and may be useful in human therapy in cancer treatment (colon cancer, melanoma). Synonyms: 2-((2S,3R,4R,5S,6R)-4-(Benzyloxy)-6-((benzyloxy)methyl)-5-((tert-butyldimethylsilyl)oxy)-2-(phenylthio)tetrahydro-2H-pyran-3-yl)-4,5,6,7-tetrachloroisoindoline-1,3-dione. CAS No. 935268-62-5. Molecular formula: C40H41Cl4NO6SSi. Mole weight: 833.72. | |
| (4-Azidophenyl)-1,3-dithiopropionate dextran | chitin synthase inhibitor. Product ID: 9-00303. Mole weight: Mw 40,000. Properties: competitive inhibitor of glucosidase I and II; pig kidney trehalase inhibitor. Reference: J. Org. Chem., 64, 1782, 1999; J. Antibiot., 44, 716, 1991; Helv. Chim. Acta, 75, 1515, 1991; Tetrahedron Lett.. 27, 2475, 1986; J. Gen. Microbiol., 137, 615, 1991; Pesticide Sci., 50, 312, 1997; Infection Immunity, 63, 4770, 1995; J. Soc. Fermentation B. | |
| 4-Methylumbelliferyl 2-acetamido-2-deoxy-a-D-glucopyranoside | 4-Methylumbelliferyl 2-acetamido-2-deoxy-a-D-glucopyranoside, a fluorogenic substrate, is primarily employed in assay development for chitinases and other glycosidases. Its utility lies in its ability to discern the substrate specificities of chitinases, alongside affording a quantitative measurement of chitinase activity. Synonyms: 4-Methylumbelliferyl N-acetyl-a-D-glucosaminide 4MU-a-GlcNAc. CAS No. 80265-04-9. Molecular formula: C18H21NO8. Mole weight: 379.36. | |
| 4-Methylumbelliferyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-galactopyranoside | 4-Methylumbelliferyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-galactopyranoside, a vital compound utilized in biomedical research, exhibits immense intricacy. Its fluorigenic substrate properties make it indispensable in studying chitinase activity, especially in relation to carbohydrate metabolism enzymes. This exceptional compound finds extensive utility in assays dedicated to comprehending the pathogenesis of diverse ailments, comprising fungal infections and inflammatory disorders. Synonyms: 4-Methylumbelliferyl 2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-beta-D-Galactopyranoside; 4-Methylumbelliferyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-galactopyranoside; [(2R,3R,4R,5R,6S)-5-acetamido-3,4-diacetyloxy-6-(4-methyl-2-oxochromen-7-yl)oxyoxan-2-yl]methyl acetate; (2R,3R,4R,5R,6S)-5-Acetamido-2-(acetoxymethyl)-6-((4-methyl-2-oxo-2H-chromen-7-yl)oxy)tetrahydro-2H-pyran-3,4-diyl diacetate; W-200973; 4-Methylumbelliferyl 2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-?-D-Galactopyranoside; [(2R,3R,4R,5R,6S)-3,4-bis(acetyloxy)-5-acetamido-6-[(4-methyl-2-oxo-2H-chromen-7-yl)oxy]oxan-2-yl]methyl acetate. CAS No. 124167-46-0. Molecular formula: C24H27NO11. Mole weight: 505.47. | |
| 4-Methylumbelliferyl 4-Deoxy-β-D-chitobiose Peracetate | 4-Methylumbelliferyl 4-Deoxy-β-D-chitobiose Peracetate is a highly noteworthy substance, serving as an indispensable instrument for studying the intricacies surrounding chitinase function. With its remarkable precision and sensitivity, this compound impeccably facilitates the identification and analysis of chitinase activity. Synonyms: 4-Methylumbelliferyl 4-Deoxy-|A-D-chitobiose Peracetate; 4-Methylumbelliferyl 4-Deoxy-beta-D-chitobiose Peracetate; [(2S,4S,5R,6S)-5-acetamido-6-[(2R,3S,4R,5R,6S)-5-acetamido-4-acetyloxy-2-(acetyloxymethyl)-6-(4-methyl-2-oxochromen-7-yl)oxyoxan-3-yl]oxy-4-acetyloxyoxan-2-yl]methyl acetate; 4-Methylumbelliferyl 4-Deoxy-b-D-chitobiose Peracetate; DTXSID50673187; 4-Methyl-2-oxo-2H-1-benzopyran-7-yl 2-acetamido-4-O-(2-acetamido-3,6-di-O-acetyl-2,4-dideoxy-beta-D-xylo-hexopyranosyl)-3,6-di-O-acetyl-2-deoxy-beta-D-glucopyranoside. CAS No. 1228931-52-9. Molecular formula: C34H42N2O15. Mole weight: 718.70. | |
| 4-Methylumbelliferyl 4-deoxychitobiose | 4-Methylumbelliferyl 4-deoxychitobiose is an incredibly valuable compound, specifically focusing on the intricate study of carbohydrates and enzyme conduct. As a fluorogenic substrate, it serves as a key facet in the appraisal of chitinases and their enzymatic behaviors. Synonyms: 4-Methylumbelliferyl 4-deoxychitobiose; 618446-98-3; 4-Methylumbelliferyl 4-Deoxy-?-D-chitobiose. CAS No. 618446-98-3. Molecular formula: C26H34N2O12. Mole weight: 566.55. | |
| 4-Methylumbelliferyl a-D-glucosaminide | 4-Methylumbelliferyl α-D-glucosaminide is a valuable tool in research for detecting chitinase activity. This substrate can be hydrolyzed by chitinases, enzymes involved in various diseases such as asthma is arthritis is and gastrointestinal disorders. Its fluorescent properties allow for easy detection and quantification, making it ideal for studying chitinase-related diseases and developing potential researchs. Synonyms: 4-Methylumbelliferyl 2-amino-2-deoxy-a-D-glucopyranoside. CAS No. 137687-00-4. Molecular formula: C16H19NO7. Mole weight: 337.32. | |
| 4-Methylumbelliferyl-β-D-N,N',N''-Triacetylchitotrioside | 4-Methylumbelliferyl-β-D-N,N',N''-triacetylchitotrioside is a fluorogenic substrate for chitinases and chitotriosidases. It is cleaved by chitinases and chitotriosidases to release the fluorescent moiety 4-methylumbelliferyl (4-MU). Synonyms: 7-[[O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1?4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1?4)-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl]oxy]-4-methyl-2H-1-benzopyran-2-one; MUF-triNAG. Grades: ≥98%. CAS No. 53643-13-3. Molecular formula: C34H47N3O18. Mole weight: 785.8. | |
| 4-Methylumbelliferyl N,N-diacetyl-b-D-chitobioside | 4-Methylumbelliferyl N,N-diacetyl-b-D-chitobioside, a remarkable biomedicine offering, thrives within the realm of the biomedical industry. Its paramount function revolves around serving as an impeccable substrate for detecting, as well as quantifying chitinase activity. This extraordinary compound devoutly aids researchers in delving into the intricacies of chitinase enzymes, thereby unraveling their involvement in multifarious biological processes. Synonyms: N,N-Diacetyl-4-methylumbelliferyl-b-D-chitobioside. CAS No. 53643-12-2. Molecular formula: C26H34N2O13. Mole weight: 582.55. | |
| 4-Methylumbelliferyl N,N,N,N-tetraacetyl-b-D-chitotetraoside | 4-Methylumbelliferyl N,N,N,N-tetraacetyl-b-D-chitotetraoside is a vital compound extensively used in biomedicine. This product plays a crucial role in the study of chitinase enzymes and their involvement in various diseases. Synonyms: GlcNAc1-b-4GlcNAc1-b-4GlcNAc1-b-4GlcNAc1-b-4MU. CAS No. 53643-14-4. Molecular formula: C42H60N4O23. Mole weight: 988.94. | |
| 4-Nitrophenyl N,N,N-triacetyl-b-D-chitotriose | 4-Nitrophenyl N,N,N-triacetyl-b-D-chitotriose is a biomedical compound of significant interest, offering immense potential in the research of diverse diseases. Remarkably, it exhibiting remarkable anti-inflammatory properties, rendering it an invaluable resource for drug development specifically targeting inflammatory ailments, including arthritis and asthma. Synonyms: 4-Nitrophenyl beta-D-N,N',N''-triacetylchitotriose; N-[2-[5-acetamido-6-[5-acetamido-4-hydroxy-2-(hydroxymethyl)-6-(4-nitrophenoxy)oxan-3-yl]oxy-4-hydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide;4-Nitrophenyl beta-D-N,N',N''-triacetylchitotriose, chitinase and lysozyme substrate; 4-Nitrophenyl 2-acetamido-2-deoxyhexopyranosyl-(1->4)-2-acetamido-2-deoxyhexopyranosyl-(1->4)-2-acetamido-2-deoxyhexopyranoside. CAS No. 7699-38-9. Molecular formula: C30H44N4O18. Mole weight: 748.69. | |
| 4-(p-Azidosalicylamido)butylamine dextran | natural chitin synthase inhibitor. Product ID: 9-00302. Mole weight: Mw 40,000. Purity: ~5 mmol substitution. Properties: selectively inhibits a-D-mannosidases 1A/B and processing of N-linked glycoproteins, competitive, active site-directed inhibitor of mammalian Golgi a-D-mannosidase I. Reference: J. Virol., 68, 7933, 1994; Arch. Biochem. Biophys., 316, 821, 1995; J. Biol. Chem., 257, 14155 1982. | |
| 5-(Biotinamido)-pentylamine | Biotincadaverine. Chitinase substrate for colorimetric assay. CAS No. 115416-38-1. Product ID: 9-00906. Molecular formula: C15H28N4O2S. Mole weight: 328.5. Properties: | |
| Allosamidin | It is produced by the strain of Streptomyces sp. Chitinase specific inhibitor. Synonyms: A82516; A-82516; beta-D-Allopyranoside, 2-(dimethylamino)-3a,5,6,6a-tetrahydro-4-hydroxy-6-(hydroxymethyl)-4H-cyclopentoxazol-5-yl 2-(acetylamino)-4-O-(2-(acetylamino)-2-deoxy-beta-D-allopyranosyl)-2-deoxy-, (3aalpha,4beta,5beta,6alpha,6aalpha)-; Allosamidine; A 82516; 1,2-Dideoxy-2'-dimethylamino-alpha-D-glucopyranoso-[2,1-d]-DELTA2'-thiazoline; CHEMBL118668; DTXSID90883122; BDBM50331851; ZINC53683592; DB04628; LS-171885; C05346; W-200706; Q27095365; (3aR,4R,5R,6S,6aS)-2-(dimethylamino)-4-hydroxy-6-(hydroxymethyl)-4,5,6,6a-tetrahydro-3aH-cyclopenta[d][1,3]oxazol-5-yl 2-(acetylamino)-4-O-[2-(acetylamino)-2-deoxy-beta-D-allopyranosyl]-2-deoxy-beta-D-allopyranoside. Grades: 99%. CAS No. 103782-08-7. Molecular formula: C25H42N4O14. Mole weight: 622.62. | |
| Antifungal peptide 2 | Antifungal peptide 2 is an antimicrobial peptide found in Eucommia ulmoides (Hardy rubber tree). It has antifungal activity. EAFP2 adopts a compact global fold composed of a 3(10) helix (Cys3-Arg6), an alpha-helix (Ala27-Cys31) and a three-stranded antiparallel beta-sheet (Cys16-Ser18, Cys23-Ser25, and Cys35-Cys37) and cross-linked by five disulfide bridges. The tertiary structure of EAFP2 shows a chitin-binding domain. Synonyms: EAFP2 (Plant defensin); Gln-Thr-Cys-Ala-Ser-Arg-Cys-Pro-Arg-Pro-Cys-Asn-Ala-Gly-Leu-Cys-Cys-Ser-Ile-Tyr-Gly-Tyr-Cys-Gly-Ser-Gly-Ala-Ala-Tyr-Cys-Gly-Ala-Gly-Asn-Cys-Arg-Cys-Gln-Cys-Arg-Gly. Grades: >98%. | |
| Argifin | Argifin is a sub-nanomolar chitinase inhibitor produced by soil microorganisms, with IC50s of 0.025 μM, 6.4 μM , 1.1 μM and 4.5 μM for SmChiA (Serratia marcescens chitinaese A), SmChiB, Aspergillus fumigatus chitinase B1 and human chitotriosidase, respectively. CAS No. 243975-37-3. Molecular formula: C29H41N9O10. Mole weight: 675.69. | |
| Asperfuran | Asperfuran is an antifungal antibiotic produced by Asperfuran oryzae. Asperfuran has fungal activity and can inhibit fungal chitin synthase, but the effect can be completely offset by lecithin. It also has inhibitory effect on HeLa S3 cells and L1210 cells. Synonyms: Asperfuran; 5,7-Benzofurandiol, 2,3-dihydro-2-(1,3-pentadienyl)-, (R-(E,E))-. CAS No. 129277-10-7. Molecular formula: C13H14O3. Mole weight: 218.25. | |
| Benzyl 2,2,2-trichloroacetimidate | Benzyl 2,2,2-Trichloroacetimidate is a reactant used in the synthesis of Allosamidin; an insect chitinase inhibitor. Synonyms: 2,2,2-Trichloroethanimidic Acid Phenylmethyl Ester; 2,2,2-Trichloroacetimidic Acid Benzyl Ester; Benzyl Trichloroacetimidate; O-Benzyl 2,2,2-Trichloroacetimidate; Benzyltrichloroacetimidate; Trichloroacetimidic Acid Benzyl Ester; Ethanimidic acid, 2,2,2-trichloro-, phenylmethyl ester. Grades: > 98 %. CAS No. 81927-55-1. Molecular formula: C9H8Cl3NO. Mole weight: 252.52. | |
| Benzyl 2,2,2-Trichloroacetimidate | Benzyl 2,2,2-Trichloroacetimidate is a reactant used in the synthesis of Allosamidin (A547900); an insect chitinase inhibitor. Group: Biochemicals. Grades: Highly Purified. CAS No. 81927-55-1. Pack Sizes: 10g, 25g. Molecular Formula: C9H8Cl3NO. US Biological Life Sciences. | Worldwide |
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