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| Product | Description | |
|---|---|---|
| Cyanogen-15N bromide | Cyanogen-15N bromide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Cyanogen-15N bromide, 63419-72-7. Product Category: Heterocyclic Organic Compound. CAS No. 63419-72-7. Molecular formula: CBrN. Mole weight: 106.91. Purity: 0.96. IUPACName: bromoformonitrile. Canonical SMILES: C(#N)Br. Product ID: ACM63419727. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Cyanogen bromide | 25g Pack Size. Group: Building Blocks, Inorganic Chemicals. Formula: CBrN. CAS No. 506-68-3. Prepack ID 16432166-25g. Molecular Weight 105.92. See USA prepack pricing. |  |
| Cyanogen bromide | 5g Pack Size. Group: Building Blocks, Inorganic Chemicals. Formula: CBrN. CAS No. 506-68-3. Prepack ID 16432166-5g. Molecular Weight 105.92. See USA prepack pricing. | |
| Cyanogen Bromide | Cyanogen bromide is a versatile solid reagent which is used widely in organic synthesis and biochemistry. Cyanogen bromide is usually written as CNBr, though this is misleading as the carbon atom has a triple bond to nitrogen and a single bond to bromine (N?C-Br). The electronegative bromine and nitrogen atoms shift electron density away from the carbon atom in this linear molecule, making it particularly electrophilic and susceptible to nucleophilic attack.The reagent has many uses in synthetic organic chemistry, being useful for the synthesis of guanidines, hydroxyguanidines, heterocyclic systems, ureas and thioureas.1CNBr is a source of electrophilic cyanide, and reacts with primary and secondary amines to yield cyanamides (1), which can be reacted further with amines or hydroxylamines to yield guanidines (2) and hydroxyguanidines (3) respectively. Group: Biochemicals. Alternative Names: Bromine Monocyanide; Bromocyan; Bromocyanide; Bromocyanogen; Campilit; NSC 89684. Grades: Highly Purified. CAS No. 506-68-3. Pack Sizes: 25g, 50g, 250g. Molecular Formula: CBrN. US Biological Life Sciences. |  Worldwide |
| Cyanogen bromide 34% w/w in dichloromethane | Cyanogen bromide 34% w/w in dichloromethane. Group: Biochemicals. Grades: Highly Purified. CAS No. 506-68-3. Pack Sizes: 100g, 250g, 500g, 1kg, 5kg. Molecular Formula: BrCN. US Biological Life Sciences. | Worldwide |
| Cyanogen bromide 50% w/w in acetone | Cyanogen bromide 50% w/w in acetone. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500g, 1kg, 2kg, 5kg, 10kg. US Biological Life Sciences. | Worldwide |
| Cyanogen bromide 50% w/w in acetonitrile | Cyanogen bromide 50% w/w in acetonitrile. Group: Biochemicals. Alternative Names: Bromine cyanide. Grades: Highly Purified. Pack Sizes: 500g, 1kg, 2kg, 5kg, 10kg. US Biological Life Sciences. | Worldwide |
| Cyanogen bromide 50% w/w in dichloromethane | Cyanogen bromide 50% w/w in dichloromethane. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 100g, 250g, 500g, 1kg, 5kg. US Biological Life Sciences. | Worldwide |
| Cyanogen bromide 50% w/w in toluene | Cyanogen bromide 50% w/w in toluene. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 250g, 500g, 1kg, 2kg, 5kg. US Biological Life Sciences. | Worldwide |
| 2-cyanogen-2-phenyl butyrate | 2-cyanogen-2-phenyl butyrate. Uses: For analytical and research use. Group: Impurity standards. CAS No. 718-71-8. Molecular Formula: C13H15NO2. Mole Weight: 217.27. Catalog: APB718718. |  |
| 4-Aminoacetophenone | A novel utilization of aminophenone derivative in toxicology, for treating intoxications with cyanogenic toxic substances. Group: Biochemicals. Alternative Names: 1-(4-Aminophenyl)ethanone; 1-(4-Aminophenyl)ethanone; 1-Acetyl-4-aminobenzene; 4-Acetylaniline; 4-Acetylphenylamine; 4-Aminophenyl Methyl Ketone; NSC 3242; p-Aminoacetophenone. Grades: Highly Purified. CAS No. 99-92-3. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| 4'-Aminoacetophenone | 4-Aminoacetophenone is a novel utilization of aminophenone derivative in toxicology, for treating intoxications with cyanogenic toxic substances. Synonyms: 1-(4-aminophenyl)ethanone; 1-(4-aminophenyl)ethanone. Grades: > 95 %. CAS No. 99-92-3. Molecular formula: C8H9NO. Mole weight: 135.16. |  |
| 4-hydroxyphenylacetaldehyde oxime monooxygenase | This enzyme is involved in the biosynthesis of the cyanogenic glucoside dhurrin in sorghum, along with EC 1.14.13.41, tyrosine N-monooxygenase and EC 2.4.1.85, cyanohydrin β-glucosyltransferase. Group: Enzymes. Synonyms: 4-hydroxybenzeneacetaldehyde oxime monooxygenase; cytochrome P450II-dependent monooxygenase; NADPH-cytochrome P450 reductase (CYP71E1); CYP71E1; 4-hydroxyphenylacetaldehyde oxime,NADPH:oxygen oxidoreductase. Enzyme Commission Number: EC 1.14.13.68. 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-0874; 4-hydroxyphenylacetaldehyde oxime monooxygenase; EC 1.14.13.68; 4-hydroxybenzeneacetaldehyde oxime monooxygenase; cytochrome P450II-dependent monooxygenase; NADPH-cytochrome P450 reductase (CYP71E1); CYP71E1; 4-hydroxyphenylacetaldehyde oxime,NADPH:oxygen oxidoreductase. Cat No: EXWM-0874. |  |
| 4-Morpholinecarbonitrile | 4-Morpholinecarbonitrile is used in the production of Rimacalib (R505015). 4-Morpholinecarbonitrile is selectively formed through a one-step nucleophilic substitution reaction of allylic tertiary amines with cyanogen bromide. Group: Biochemicals. Grades: Highly Purified. CAS No. 1530-89-8. Pack Sizes: 1g, 5g. Molecular Formula: C5H8N2O, Molecular Weight: 112.13. US Biological Life Sciences. | Worldwide |
| aliphatic (R)-hydroxynitrile lyase | The enzyme contains Zn2+. The enzyme catalyses the stereoselective synthesis of aliphatic (R)-cyanohydrins. No activity towards mandelonitrile and 4-hydroxymandelonitrile. Natural substrates for the (R)-oxynitrilase from Linum usitatissimum are acetone and butan-2-one, which are the building blocks of the cyanogen glycosides in Linum, linamarin and lotaustralin, or linustatin and neolinustatin, respectively. Group: Enzymes. Synonyms: (R)-HNL; (R)-oxynitrilase; (R)-hydroxynitrile lyase; LuHNL. Enzyme Commission Number: EC 4.1.2.46. 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-4882; aliphatic (R)-hydroxynitrile lyase; EC 4.1.2.46; (R)-HNL; (R)-oxynitrilase; (R)-hydroxynitrile lyase; LuHNL. Cat No: EXWM-4882. | |
| Cyanamide | Cyanamide is used in the synthesis of H2 receptor histamine antagonists. Also use in the synthesis of oxadiazoles and 1,2,4-thiaziazoles as dual 5-lipoxygenase and cyclooxygenase inhibitors. Group: Biochemicals. Alternative Names: Alzogur; Amidocyanogen; Carbamonitrile; Carbimide; Cyanamide F 1000; Cyanoamine; Cyanogen nitride; Cyanogenamide; Deurbraak; Dormex; F 1000; Hydrogen cyanamide; N-Cyanoamine; NSC 24133; TsAKS. Grades: Highly Purified. CAS No. 420-04-2. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| cyanohydrin β-glucosyltransferase | Acts on a wide range of substrates in vitro, including cyanohydrins, terpenoids, phenolics, hexanol derivatives and plant hormones, in a regiospecific manner. This enzyme is involved in the biosynthesis of the cyanogenic glucoside dhurrin in sorghum, along with EC 1.14.13.41, tyrosine N-monooxygenase and EC 1.14.13.68, 4-hydroxyphenylacetaldehyde oxime monooxygenase. This reaction prevents the disocciation and release of toxic hydrogen cyanide. Group: Enzymes. Synonyms: uridine diphosphoglucose-p-hydroxymandelonitrile glucosyltransferase; UDP-glucose-p-hydroxymandelonitrile glucosyltransferase; uridine diphosphoglucose-cyanohydrin glucosyltransferase; uridine diphosphogluc. Enzyme Commission Number: EC 2.4.1.85. CAS No. 55354-52-4. 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-2625; cyanohydrin β-glucosyltransferase; EC 2.4.1.85; 55354-52-4; uridine diphosphoglucose-p-hydroxymandelonitrile glucosyltransferase; UDP-glucose-p-hydroxymandelonitrile glucosyltransferase; uridine diphosphoglucose-cyanohydrin glucosyltransferase; uridine diphosphoglucose:aldehyde cyanohydrin β-glucosyltransferase; UDP-glucose:(S)-4-hydroxymandelonitrile β-D-glucosyltransferase; UGT85B1; UDP-glucose:p-hydroxymandelonitrile-O-glucosyltransferase. Cat No: EXWM-2625. | |
| isoleucine N-monooxygenase | A heme-thiolate protein (P-450). This enzyme catalyses two successive N-hydroxylations of L-isoleucine, the first committed steps in the biosynthesis of the cyanogenic glucoside lotaustralin in the plant Lotus japonicus. The product of the two hydroxylations, N,N-dihydroxy-L-isoleucine, is extremely labile and dehydrates spontaneously. The dehydrated product is then subject to a decarboxylation that produces the oxime. It is still not known whether the decarboxylation is spontaneous or catalysed by the enzyme. The product, (E)-2-methylbutanal oxime, undergoes a spontaneous isomerization to the (Z) form. The enzyme can also accept L-valine as substrate, with a lower activity. It is different from EC 1.14.13.118 (valine N-monooxygenase), which prefers L-valine. Group: Enzymes. Synonyms: CYP79D3; CYP79D4. Enzyme Commission Number: EC 1.14.13.117. 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-0717; isoleucine N-monooxygenase; EC 1.14.13.117; CYP79D3; CYP79D4. Cat No: EXWM-0717. | |
| Lotaustralin | Lotaustralin is a cyanogenic glucoside isolated from Manihot esculenta [1]. Uses: Scientific research. Group: Natural products. CAS No. 1973415-50-7. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N5079. |  |
| Native Almonds Mandelonitrile Lyase | In enzymology, a mandelonitrile lyase is an enzyme that catalyzes the chemical reaction:mandelonitrile<-> hydrogen cyanide + benzaldehyde. Hence, this enzyme has one substrate, mandelonitrile, and two products, hydrogen cyanide and benzaldehyde. This enzyme belongs to the family of lyases, specifically the aldehyde-lyases, which cleave carbon-carbon bonds. This enzyme participates in cyanoamino acid metabolism. It has 2 cofactors:flavin, and flavoprotein. Mandelonitrile lyase is a cyanogenic enzyme. Applications: Mandelonitrile lyase from almonds has been used in a study to assess the apoplastic antioxidant system in prunus. it has also been used in a study to investigate screening for new hydroxynitrilases from plants. Group: Enzymes. Synonyms: mandelonitrile lyase; EC 4.1.2.10; (R)-oxynit. Enzyme Commission Number: EC 4.1.2.10. CAS No. 9024-43-5. PhaMDL. Activity: 80-240 units/mg protein (biuret). Storage: 2-8°C. Form: ammonium sulfate suspension; Suspension in 50 mM imidazole, 2.8 M (NH4)2SO4, pH 6.0. Source: Almonds. mandelonitrile lyase; EC 4.1.2.10; (R)-oxynitrilase; oxynitrilase; D-oxynitrilase; D-α-hydroxynitrile lyase; mandelonitrile benzaldehyde-lyase; PaHNL; AtHNL; PhaMDL; (R)-HNL; (R)-PeHNL; (R)-hydroxynitrile lyase; R-selective hydroxynitrile lyase; R-selective HNL; (R)-(+)-mandelonitrile lyase; 9024-43-5. Cat No: NATE-0557. | |
| Rhodiocyanoside A | Rhodiocyanoside A is a cyanogenic glucoside found in the Rhodiola quadrifida with inhibitory activity against histamine. Synonyms: (2Z)-4-(beta-D-glucopyranosyloxy)-2-methylbut-2-enenitrile; (2Z)-2-methyl-4-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}but-2-enenitrile. Grades: >98%. CAS No. 168433-86-1. Molecular formula: C11H17NO6. Mole weight: 259.258. | |
| (S)-Prunasin | It is useful to the synthesis of cyanogen glycoside, a component contains in antiperspirants, deodorants, body soaps, shampoos, hair rinses, and hair, which inhibits volatile steroid formation by resident bacteria. Uses: Used in the synthesis of cyanogen glycoside. a component contains in antiperspirants, deodorants, body soaps, shampoos, hair rinses, and hair. Synonyms: (α S) -α - (β -D-Glucopyranosyloxy) benzeneacetonitrile; L-Prunasin; Sambunigrin; (2S)-Sambunigrin. Grades: 95%. CAS No. 99-19-4. Molecular formula: C14H17NO6. Mole weight: 295.29. | |
| tyrosine N-monooxygenase | A heme-thiolate protein (P-450). This enzyme is involved in the biosynthesis of the cyanogenic glucoside dhurrin in sorghum, along with EC 1.14.13.68, 4-hydroxyphenylacetaldehyde oxime monooxygenase and EC 2.4.1.85, cyanohydrin β-glucosyltransferase. Some 2-(4-hydroxyphenyl)-1-nitroethane is formed as a side product. Group: Enzymes. Synonyms: tyrosine N-hydroxylase; CYP79A1. Enzyme Commission Number: EC 1.14.13.41. CAS No. 159447-19-5. 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-0849; tyrosine N-monooxygenase; EC 1.14.13.41; 159447-19-5; tyrosine N-hydroxylase; CYP79A1. Cat No: EXWM-0849. | |
| valine N-monooxygenase | A heme-thiolate protein (P-450). This enzyme catalyses two successive N-hydroxylations of L-valine, the first committed steps in the biosynthesis of the cyanogenic glucoside linamarin in Manihot esculenta (cassava). The product of the two hydroxylations, N,N-dihydroxy-L-valine, is extremely labile and dehydrates spontaneously. The dehydrated product is then subject to a decarboxylation that produces the oxime. It is still not known whether the decarboxylation is spontaneous or catalysed by the enzyme. The product, (E)-2-methylpropanal oxime, undergoes a spontaneous isomerization to the (Z) form. The enzyme can also accept L-isoleucine as substrate, with a lower activity. It is different from EC 1.14.13.117 (isoleucine N-monooxygenase), which prefers L-isoleucine. Group: Enzymes. Synonyms: CYP79D1; CYP79D2. Enzyme Commission Number: EC 1.14.13.118. 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-0718; valine N-monooxygenase; EC 1.14.13.118; CYP79D1; CYP79D2. Cat No: EXWM-0718. | |
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