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| Product | Description | |
|---|---|---|
| 1,2,2,6,6-Pentamethylpiperidine | 1,2,2,6,6-Pentamethylpiperidine is a ganglion-blocking drug. It is one of the most strongly basic tertiary amine. It is ued as an oral treatment for hypertension and used as an organic structure directing agent (OSDA) in the synthesis of the RTH-type zeolites. It is also used in the synthesis of BN-fused polycyclic aromatic molecules for potential application to electronic materials and apparatus. It is also a catalyst for the chemoselective silylation of benzylic alcohols. Uses: 1,2,2,6,6-pentamethylpiperidine is ued as an oral treatment for hypertension and used as an organic structure directing agent (osda) in the synthesis of the rth-type zeolites. it is also used in the synthesis of bn-fused polycyclic aromatic molecules for potential application to electronic materials and apparatus. Synonyms: 1,2,2,6,6-pentamethylpiperidine. Grades: > 98 %. CAS No. 79-55-0. Molecular formula: C10H21N. Mole weight: 155.28. |  |
| 1, 3-Diaminotetrafluoro Benzene | 1, 3-Diaminotetrafluoro Benzene is used for carcinogenicity and toxicity testing for aromatic amines. Also in the prepartion of tissue adhesive composition, e.g. (use of polyurethane adhesive in closing incisions). Group: Biochemicals. Grades: Highly Purified. CAS No. 1198-63-6. Pack Sizes: 100mg, 250mg. Molecular Formula: C6H4F4N2, Molecular Weight: 180.1. US Biological Life Sciences. |  Worldwide |
| 1,5-Diaminonaphthalene | Aromatic amines likely to have high carcinogenic potency. QSARs of aromatic amines. Group: Biochemicals. Alternative Names: 1,5-DAN; 1,5-Diaminonaphthalene; 1,5-Naphthylenediamine; NSC 401110. Grades: Highly Purified. CAS No. 2243-62-1. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| 1,5-Diaminonaphthalene-d6 | 1,5-Diaminonaphthalene. Aromatic amines likely to have high carcinogenic potency. QSARs of aromatic amines. Group: Biochemicals. Alternative Names: 1,5-DAN-d6; 1,5-Diaminonaphthalene-d6; 1,5-Naphthylenediamine-d6; NSC 401110-d6. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| 1,7-Dimethyl-1H-imidazo[4,5-g]quinoxalin-2-amine. | An abundant mutagenic heterocyclic aromatic amine (HAA) formed in cooked beef and other meats. Group: Biochemicals. Alternative Names: 2-Amino-1,7-dimethyl-1H-imidazo[4,5-g]quinoxaline; 7-MeIgQx. Grades: Highly Purified. CAS No. 934333-16-1. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| (1R,2R)-(-)-N-p-Tosyl-1,2-diphenylethylenediamine | (1R,2R)-(-)-N-p-Tosyl-1,2-diphenylethylenediamine (CAS# 144222-34-4) is used as a catalyst in stereoselective preparation of aromatic ketone derivatives as well as other chiral organic compounds. Synonyms: N-[(1R,2R)-2-amino-1,2-diphenylethyl]-4-methylbenzenesulfonamide; N-[(1R,2R)-2-amino-1,2-diphenylethyl]-4-methylbenzenesulfonamide. Grades: ≥ 98 %, ≥ 95 % e.e. CAS No. 144222-34-4. Molecular formula: C21H22N2O2S. Mole weight: 366.48. | |
| 2,4-Diaminotoluene | Aromatic amines likely to have high carcinogenic potency. QSARs of aromatic amines. Group: Biochemicals. Grades: Highly Purified. CAS No. 95-80-7. Pack Sizes: 1g, 10g, 50g. Molecular Formula: C?H??N?. US Biological Life Sciences. | Worldwide |
| 2,4-Diaminotoluene-13C6 | 2,4-Diaminotoluene-13C6 is a isotope labelled analog of 2,4-Diaminotoluene (D416780). 2,4-Diaminotoluene is an aromatic amines likely to have high carcinogenic potency. QSARs of aromatic amines. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C13C6H10N2. US Biological Life Sciences. | Worldwide |
| 2,4-Diaminotoluene-d3 | 2,4-Diaminotoluene. Aromatic amines likely to have high carcinogenic potency. QSARs of aromatic amines. Group: Biochemicals. Alternative Names: 4-(Methyl-d3)-1,3-benzenediamine; Toluene-2,4-diamine-d3; 1,3-Diamino-4-(methyl-d3)benzene; 2,4-Diamino-1-(methyl-d3)benzene; 2,4-Tolylenediamine-d3; 3-Amino-4-(methyl-d3)aniline; 4-(Methyl-d3)-1,3-benzendiamine; 4-(Methyl-d3)-1,3-benzenediamine; 4-(Methyl-d3)-1,3-phenylenediamine; 4-(Methyl-d3)-m-phenylenediamine; Eucanine GB-d3; Fouramine J-d3; Fourrine M-d3; Pelagol J-d3; Renal MD-d3; TDA-d3; Zoba GKE-d3; m-Toluenediamine-d3; m-Tolylenediamine-d3. Grades: Highly Purified. CAS No. 71111-08-5. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| 2,6-Diaminotoluene | Aromatic amines likely to have high carcinogenic potency. QSARs of aromatic amines. Group: Biochemicals. Alternative Names: 2-Methyl-1,3-benzenediamine; Toluene-2,6-diamine; 1,3-Diamino-2-methylbenzene; 2,6-Diamino-1-methylbenzene; 2,6-Toluylenediamine; 2,6-Tolylenediamine; 2-Methyl-1,3-benzenediamine; 2-Methyl-1,3-phenylenediamine; 2-Methyl-m-phenylenediamine; NSC 147490. Grades: Highly Purified. CAS No. 823-40-5. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| 2,6-Diaminotoluene-13C6 | 2,6-Diaminotoluene-13C6 is labelled 2,6-Diaminotoluene which is an aromatic amine likely to have high carcinogenic potency. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 10mg. Molecular Formula: C13C6H10N2. US Biological Life Sciences. | Worldwide |
| 2,6-Diaminotoluene-d3 | Labeled 2,6-Diaminotoluene. Aromatic amines likely to have high carcinogenic potency. QSARs of aromatic amines. Group: Biochemicals. Alternative Names: 2-(Methyl-d3)-1,3-benzenediamine; Toluene-2,6-diamine-d3; 1,3-Diamino-2-(methyl-d3)benzene; 2,6-Diamino-1-(methyl-d3)benzene; 2,6-Toluylenediamine-d3; 2,6-Tolylenediamine-d3; 2-(Methyl-d3)-1,3-benzenediamine; 2-(Methyl-d3)-1,3-phenylenediamine; 2-(Methyl-d3)-m-phenylenediamine; NSC 147490-d3. Grades: Highly Purified. CAS No. 362049-58-9. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| 2-Amino-3,4-dimethylimidazo[4,5-f]quinoxaline | 2-Amino-3,4-dimethylimidazo[4,5-f]quinoxaline is used in analytical studies to identify abundant mutagenic heterocyclic aromatic amine that are formed in cooked beef. Group: Biochemicals. Grades: Highly Purified. CAS No. 108354-48-9. Pack Sizes: 5mg, 50mg. Molecular Formula: C11H11N5, Molecular Weight: 213.24. US Biological Life Sciences. | Worldwide |
| 2-Amino-3,4-dimethylimidazo[4,5-f]quinoxaline-d3 | 2-Amino-3,4-dimethylimidazo[4,5-f]quinoxaline-d3 is an isotope labelled analog of 2-Amino-3,4-dimethylimidazo[4,5-f]quinoxaline. 2-Amino-3,4-dimethylimidazo[4,5-f]quinoxaline is used in analytical studies to identify abundant mutagenic heterocyclic aromatic amine that are formed in cooked beef. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 10mg. Molecular Formula: C11H8D3N5, Molecular Weight: 216.26. US Biological Life Sciences. | Worldwide |
| 2-Amino-4,6-dichloro-s-triazine | An aromatic intermediate compound useful for the preparation of substituted melamine, ammelides, and ammelines. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| 2-Amino-4,6-dichloro-s-triazine-13C3 | 2-Amino-4,6-dichloro-s-triazine-13C3 is the isotopic analog of 2-Amino-4,6-dichloro-s-triazine (A604750). 2-Amino-4,6-dichloro-s-triazine is an aromatic intermediate compound useful for the preparation of substituted melamine, ammelides, and ammelines. 2-Amino-4,6-dichloro-s-triazine-13C3 is the intermediate in the synthesis of Ammelide -13C3 (A633652). Ammelide -13C3 is a labelled related compound of Melamine. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: 13C3H2Cl2N4. US Biological Life Sciences. | Worldwide |
| 2-Amino-4-hydroxy-6-chloro-s-triazine | An aromatic intermediate compound useful for the preparation of substituted melamine, ammelides, and ammelines. Group: Biochemicals. Alternative Names: 4-Amino-6-chloro-1,3,5-triazin-2(1H)-one; 2-Amino-4-chloro-6-hydroxy-s-triazine; NSC 269402. Grades: Highly Purified. CAS No. 38862-29-2. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| 2-Amino-5-phenylpyridine | 2-Amino-5-phenylpyridine is a mutagenic heterocyclic aromatic amine that is formed by pyrolysis of phenylalanine in proteins. 2-Amino-5-phenylpyridine is in broiled sardines and is considered as potentially carcinogenic [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 33421-40-8. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-W002820. |  |
| 2-Aminodibenzofuran | 2-Aminodibenzofuran is a polycyclic aromatic hydrocarbon (PAH) used in the preparation of mono and bisazo dyes. 2-Aminodibenzofuran is a carcinogen. Group: Biochemicals. Alternative Names: 2-Dibenzofuranamine; NSC 402280; 2-Aminodiphenylene Oxide. Grades: Highly Purified. CAS No. 3693-22-9. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| 2-Chloroaniline-15N | 2-Chloroaniline-15N is the isotope labelled analog of 2-Chloroaniline (C364372), an halogenated aromatic amine compound used as a building block for the production of various pesticides, pharmaceuticals and dyes. Group: Biochemicals. Grades: Highly Purified. CAS No. 36238-55-8. Pack Sizes: 5mg, 25mg. Molecular Formula: C6H6Cl15N. US Biological Life Sciences. | Worldwide |
| 2-(Dicyclohexylphosphino)biphenyl | Ligand used in the palladium-catalyzed synthesis of aromatic amines from aryl chlorides, bromides and triflates. Ligand employed in Suzuki coupling reactions involving aryl chlorides, bromides and triflates. Useful ligand for the Pd-catalyzed oxidation of alcohols in the presence of chlorobenzenes. Useful ligand for the Pd-catalyzed amination with ammonia equivalents. Ligand for the gold(I)-catalyzed intramolecular [4+2] cycloadditions involving 1,3-enynes and arylalkynes with alkenes. Ligand used in the palladium-catalyzed borylation of aryl bromdies. Ligand used in the palladium-catalyzed siliylation of aryl chlorides. Group: Organic phosphine compounds. Alternative Names: Cyclohexyl JohnPhos. CAS No. 247940-06-3. Molecular formula: C24H31P. Mole weight: 350.48. Appearance: Solid. Purity: 0.98. IUPACName: dicyclohexyl-(2-phenylphenyl)phosphane. Canonical SMILES: C1CCC (CC1)P (C2CCCCC2)C3=CC=CC=C3C4=CC=CC=C4. ECNumber: 480-030-2. Catalog: ACM247940063-1. |  |
| 2-(Di-tert-butylphosphino)biphenyl | Ligand used in the palladium-catalyzed synthesis of aromatic amines from aryl chlorides, bromides and triflates. Ligand employed in a very active and general catalyst for Suzuki coupling reactions using aryl chlorides, bromides and triflates. Ligand used in palladium-catalyzed synthesis of oxindoles from α-chloroacetanilides. Effective ligand used in palladium-catalyzed arylation of thiazoles. Used in the formation of 2-benzylindolines via sequential palladium-catalyzed N-arylation/cyclization/C-arylation. Selective in the palladium-catalyzed arylation of silyl enol ethers formed from copper-catalyzed reduction of enones. Group: Organic phosphine compounds. Alternative Names: (2-Biphenylyl)-Di-Tert-Butylphosphine. CAS No. 224311-51-7. Molecular formula: C20H27P. Mole weight: 298.4. Appearance: Solid. Purity: 0.98. IUPACName: ditert-butyl-(2-phenylphenyl)phosphane. Canonical SMILES: CC (C) (C)P (C1=CC=CC=C1C2=CC=CC=C2)C (C) (C)C. Density: 1 g/cm3. Catalog: ACM224311517-1. | |
| 2-Ethyl-2-methoxyhexyl Salicylate | 2-Ethyl-2-methoxyhexyl Salicylate is made from 3-Heptanone which is versatile synthetic building block. It was used in the synthesis of semicarbazone and thiosemicarbazone derivatives with antimalarial activity. 3-Heptanone was also used as reactant in enantioselective organocatalytic reductive amination of aliphatic ketones with aromatic amines using benzothiazoline hydrogen donor. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg, 25mg. Molecular Formula: C16H24O4, Molecular Weight: 280.36. US Biological Life Sciences. | Worldwide |
| 2-[(p-chlorobenzyl)amino]-pyridine | 2-[(p-chlorobenzyl)amino]-pyridine is a useful synthetic intermediate. It can be prepared via selective iridium-catalyzed alkylation of (hetero)aromatic amines. Group: Biochemicals. Grades: Highly Purified. CAS No. 22881-33-0. Pack Sizes: 500mg, 5g. Molecular Formula: C12H11ClN2. US Biological Life Sciences. | Worldwide |
| 2-Toluidine | A carcinogenic and toxic aromatic amine contained in hair dye, henna and dyed hair samples. Group: Biochemicals. Alternative Names: o-Toluidine; 1-Amino-2-methylbenzene; 2-Amino-1-methylbenzene; 2-Aminotoluene; 2-Methyl-1-aminobenzene; 2-Methylaniline; 2-Methylbenzenamine; 2-Methylphenylamine; 2-Tolylamine; NSC 15348; o-Aminotoluene; o-Methylaniline; o-Methylbenzenamine. Grades: Highly Purified. CAS No. 95-53-4. Pack Sizes: 10ml. US Biological Life Sciences. | Worldwide |
| 2-Toluidine-13C6 | A labeled carcinogenic and toxic aromatic amine contains in hair dye, henna and dyed hair samples. Group: Biochemicals. Alternative Names: o-Toluidine-13C; 1-Amino-2-methylbenzene-13C; 2-Amino-1-methylbenzene-13C; 2-Aminotoluene-13C; 2-Methyl-1-aminobenzene-13C; 2-Methylaniline-13C; 2-Methylbenzenamine-13C; 2-Methylphenylamine-13C; 2-Tolylamine-13C; NSC 15348-13C; o-Aminotoluene-13C; o-Methylaniline-13C; o-Methylbenzenamine-13C. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| 3-Azido-5-methyl-2-furancarboxaldehyde | 3-Azido-5-methyl-2-furancarboxaldehyde is an intermediate in the synthesis of 2-Amino-1,6-dimethylfuro[3,2-e]imidazo[4,5-b]pyridine (A605070), a heterocyclic aromatic amines (HAAs) as potential human carcinogen. 2933. 29. 9000. Group: Biochemicals. Grades: Highly Purified. CAS No. 213178-20-2. Pack Sizes: 500ug, 1mg. Molecular Formula: C6H5N3O2. US Biological Life Sciences. | Worldwide |
| 3-Bromo-5-methyl-2-furancarboxaldehyde | 3-Bromo-5-methyl-2-furancarboxaldehyde is an intermediate in the synthesis of 2-Amino-1,6-dimethylfuro[3,2-e]imidazo[4,5-b]pyridine (A605070), a heterocyclic aromatic amines (HAAs) as potential human carcinogen. 2933. 29. 9000. Group: Biochemicals. Grades: Highly Purified. CAS No. 183562-13-2. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C6H5BrO2. US Biological Life Sciences. | Worldwide |
| 3-Chloro-4-nitro-2-naphthalenecarboxylic Acid | 3-Chloro-4-nitro-2-naphthalenecarboxylic Acid is a versatile reactant derived from β-Naphthylamine-3-carboxylic Acid (N378050), which is an unnatural aromatic amino acid, that can be used for the manufacture of more complex compounds. β-Naphthylamine-3-carboxylic Acid can be utilized for the synthesis of novel acronycine/duocarmycin hybrid natural product. Group: Biochemicals. Grades: Highly Purified. CAS No. 498546-34-2. Pack Sizes: 100mg, 250mg. Molecular Formula: C11H6ClNO4, Molecular Weight: 251.62. US Biological Life Sciences. | Worldwide |
| 3-Methyl-4-nitrobiphenyl | Aromatic amine with carcinogenic and mutagenic properties. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| 4,4'-Dimethoxydiphenylamine | 4,4'-Dimethoxydiphenylamine is an aromatic amine that is used as a hole transporting material that facilitates efficiency mobility of charges in an electrochemical device. Uses: It can be used as a hole transporting material in the synthesis of 4,4'-dimethoxydiphenylamine-substituted 9,9'- bifluorenylidene with a power efficiency of ~18% which may be used in combination with an electron transporting layer in the fabrication of polymeric solar cells. it may also be used in the preparation of dimethyldiphenylamino functionalized carbazoles as electronically active materials which can potentially be used in the development of optoelectronic devices. Group: Small molecule semiconductor building blockselectroluminescence materials other electronic materials synthetic tools and reagents polymers. Alternative Names: Bis(p-methoxyphenyl)amine. CAS No. 101-70-2. Pack Sizes: Packaging 1, 5 g in glass bottle. Product ID: 4-Methoxy-N-(4-methoxyphenyl)aniline. Molecular formula: 229.27. Mole weight: C14H15NO2. COC1=CC=C(C=C1)NC2=CC=C(C=C2)OC. InChI=1S/C14H15NO2/c1-16-13-7-3-11 (4-8-13)15-12-5-9-14 (17-2)10-6-12/h3-10, 15H, 1-2H3. VCOONNWIINSFBA-UHFFFAOYSA-N. 95%+. |  |
| 4-Amino-3-methylbiphenyl | Aromatic amine with carcinogenic and mutagenic properties. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| 4-Amino-3-methylbiphenyl-2,3,4,5,6-d5 | Aromatic amine with carcinogenic and mutagenic properties. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| 4-Amino-3-methylbiphenyl, Hydrochloride | Aromatic amine with carcinogenic and mutagenic properties. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| 4-Aminobenzoic acid | 4-Aminobenzoic acid, also known as para-aminobenzoic acid (PABA), is utilized as a precursor in the synthesis of aromatic amines and azo dyes. Uses: 4-aminobenzoic acid is used: as a building block in the synthesis of polyamides as a substrate in folic acid production in the synthesis of schiff base as an organic ligand in metal-organic framework (mofs) synthesis. Group: Amino acids. Alternative Names: para-Aminobenzoic acid, PABA, Vitamin Bx, Vitamin H1. CAS No. 150-13-0. Molecular formula: H2NC6H4CO2H. Mole weight: 137.14. Appearance: White to off white crystalline powder. IUPACName: 4-aminobenzoic acid. Canonical SMILES: Nc1ccc(cc1)C(O)=O. Density: 1.374. ECNumber: 205-753-0. Catalog: ACM150130-4. | |
| 4-Chloro-2-nitroaniline | A nitro-aromatic amine with mutagenicity and carcinogenicity. Group: Biochemicals. Alternative Names: 4-Chloro-2-nitrobenzenamine; (4-Chloro-2-nitrophenyl)amine. Grades: Highly Purified. CAS No. 89-63-4. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| 4-Hydroxydiphenylamine | 4-Hydroxydiphenylamine (p-Anilinophenol; 4-Hydroxy-DPA) is an aromatic amine organic compound. 4-Hydroxydiphenylamine has antioxidant activity and is also used as a catalyst or intermediate in some chemical reactions to synthesize other compounds. 4-Hydroxydiphenylamine can be used in the research of environmental science and toxicology [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: p-Anilinophenol; 4-Hydroxy-DPA. CAS No. 122-37-2. Pack Sizes: 10 mM * 1 mL; 5 g; 10 g; 25 g. Product ID: HY-W088320. | |
| 4-Morpholinoaniline | 4-Morpholinoaniline is a morpholine derivative used in the preparation of central nervous system (CNS) active agents. 4-Morpholinoaniline is also one of the primary aromatic amines used in the colour developing process in photographs. Group: Biochemicals. Alternative Names: (4- (Morpholino) phenyl) amine; 4- (4-Aminophenyl) morpholine; 4-(4-Morpholinyl)aniline; 4- (4-Morpholinyl) benzenamine; 4-(Morpholin-4-yl)phenylamine; 4-Morpholinobenzenamine; 4-N-Morpholinoaniline; N- (4-Aminophenyl) morpholine; N- (4'-Aminophenyl) morpholine; NSC 26334; p-Morpholinoaniline. Grades: Highly Purified. CAS No. 2524-67-6. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| 5H-Pyrido[3,2-b]indole | 5H-Pyrido[3,2-b]indole. Uses: Novel aromatic amine compound for organic electroluminescent device, illuminating device and display. Group: Small molecule semiconductor building blocksorganic light-emitting diode (oled) materials synthetic tools and reagents semiconductor blocks. Alternative Names: δ-Carboline. CAS No. 245-08-9. Pack Sizes: 250 mg in glass bottle. Product ID: 5H-pyrido[3,2-b]indole. Molecular formula: 168.2. Mole weight: C11H8N2. C1(C=CC=C2)=C2C(N=CC=C3)=C3N1. InChI=1S/C11H8N2/c1-2-5-9-8 (4-1)11-10 (13-9)6-3-7-12-11/h1-7, 13H. NSBVOLBUJPCPFH-UHFFFAOYSA-N. >98.0%(HPLC). | |
| 5H-Pyrido[3,2-b]indole | Novel aromatic amine compound for organic electroluminescent device, illuminating device and display. Group: Organic & printed electronics. Alternative Names: δ-Carboline. CAS No. 245-08-9. Molecular formula: C11H8N2. Mole weight: 168.2. Appearance: White to Yellow to Green powder to crystal. Purity: >98.0%(HPLC). IUPACName: 5H-pyrido[3,2-b]indole. Canonical SMILES: C1(C=CC=C2)=C2C(N=CC=C3)=C3N1. Density: 1.301g/cm3. Catalog: ACM245089. | |
| 5-Hydroxytryptophan | 5-Hydroxytryptophan, a tryptophan metabolite, is a direct 5-hydroxytryptamine (5-HT) precursor and an L-aromatic amino acid decarboxylase substrate. [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: 5-HTP; DL-5-Hydroxytryptophan. CAS No. 56-69-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0122. | |
| (6R)-5,6,7,8-Tetrahydro-L-biopterin 2HCl | Tetrahydrobiopterin is a naturally occurring essential cofactor of the three aromatic amino acid hydroxylase enzymes, used in the degradation of amino acid phenylalanine and in the biosynthesis of the neurotransmitters serotonin, melatonin, dopamine, norepinephrine , epinephrine, and is a cofactor for the production of nitric oxide by the nitric oxide synthases. Chemically, its structure is that of a reduced pteridine derivative. Group: Biochemicals. Alternative Names: (6R)-5,6,7,8-Tetrahydrobiopterin dihydrochloride; 6R-BH4; Sapropterin; Sapropterin dihydrochloride; BioMarin T 1401, Biopten, Kuvan, SUN 0588; Shiratori SN 0588. Grades: Highly Purified. CAS No. 69056-38-8,17528-72-2. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C?H??N?O?; 2(HCl), Molecular Weight: 314.17. US Biological Life Sciences. | Worldwide |
| 7,8-Dihydro-L-biopterin-d3 | 7,8-Dihydro-L-biopterin-d3 is a labeled reduced form of Biopterin. An oxidation product of tetrahydrobiopterin, a naturally occurring cofactor of the aromatic amino acid hydroxylase, is involved in the synthesis of tyrosine and neurotransmitters dopamine and serotonin. It is a noncompetitive inhibitor of GTP cyclohydrolase I, with a Ki of 14.4 μM. Applications: Noncompetitive inhibitor of gtp cyclohydrolase i. Group: Coenzymes. Synonyms: 2-Amino-6-[(1R,2S)-1,2-dihydroxypropyl]-7,8-dihydro-4(3H)-pteridinone; 7,8-Dihydrobiopterin. CAS No. 6779-87-9 (unlabeled). Mole weight: 242.25. Form: Solid. 2-Amino-6-[(1R,2S)-1,2-dihydroxypropyl]-7,8-dihydro-4(3H)-pteridinone; 7,8-Dihydrobiopterin; 7,8-Dihydro-L-biopterin-d3; 6779-87-9 (unlabeled). Cat No: COEC-091. |  |
| AHR Antagonist 5 | AHR Antagonist 5, an effective and orally active aromatic hydrocarbon receptor (AHR) antagonist with IC50 of less than 0.5 μM. It can significantly inhibit tumor growth in combination with the checkpoint inhibitor anti-PD-1. Synonyms: BCP33104; HY-136220; CS-0120848; (R)-N-(2-(5-Fluoropyridin-3-Yl)-8-Isopropylpyrazolo[1,5-A][1,3,5]Triazin-4-Yl)-2,3,4,9-Tetrahydro-1H-Carbazol-3-Amine Trihydrochloride. Grades: ≥98% by HPLC. CAS No. 2247953-39-3. Molecular formula: C25H27Cl3FN7. Mole weight: 550.9. | |
| Allyl[1, 3-bis (2, 6-diisopropylphenyl) -2-imidazolidinylidene]chloropalladium (II) | Catalyst for the cross-coupling of aryl chlorides or bromides with aromatic amines. Catalyst for the α-arylation of ketones. Catalyst for anaerobic alcohol oxidation. Group: Heterocyclic organic compound. Alternative Names: ALLYLCHLORO[1,3-BIS(2,6-DI-I-PROPYLPHENYL)-4,5-DIHYDROIMIDAZOL-2-YLIDENE]PALLADIUM (II); Allylchloro[1, 3-bis (2, 6-di-i-propylphenyl)-4, 5-dihydroimidazol-2-ylidene]palladium (II), 97%; ALLYLCHLORO[1, 3-BIS- (DIISOPROPYLPHENYL)-2-IMIDAZOLIDINYLIDENE]PALLADIUM (II). CAS No. 478980-01-7. Molecular formula: C30H43ClN2Pd. Mole weight: 573.55. Purity: 0.96. IUPACName: Allylchloro[1,3-bis(2,6-di-i-propylphenyl)-4,5-dihydroimidazol-2-ylide. Catalog: ACM478980017. | |
| α -[2- (Methylamino) ethyl]benzyl Alcohol | α -[2- (Methylamino) ethyl]benzyl Alcohol is an aromatic amino alcohol used as an initiator in radical addition reactions with tetrahalomethanes. Group: Biochemicals. Alternative Names: (±)-N-Methyl-3-hydroxy-3-phenylpropylamine; 3-(Methylamino)-1-phenyl-1-propanol; 3-Hydroxy-N-methyl-3-phenylpropylamine; 3-Methylamino-1-phenylpropanol; N- (3-Hydroxy-3-phenylpropyl) methylamine; N-Methyl-3-hydroxy-3-phenylpropylamine; N-Methyl-3-phenyl-3-hydroxypropylamine; α -[2- (Methylamino) ethyl]benzenemethanol; N-Methyl-N-(3-hydroxy-3-phenylpropyl)amine. Grades: Highly Purified. CAS No. 42142-52-9. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| Ammonium Cerium(IV) Nitrate | Ammonium cerium(IV) nitrate is used to detect the amount of aromatic amines and phenolic compounds in a variety of samples. Ammonium cerium(IV) nitrate is also used as a reagent to synthesize amide anhydrovinblastine analogues (e.g. Anhydrovinblastine NÂb-oxide sulfate salt [A659755]) as anti-tumor agents. Group: Biochemicals. Grades: Highly Purified. CAS No. 16774-21-3. Pack Sizes: 10g, 25 g. Molecular Formula: CeH8N8O18, Molecular Weight: 548.22. US Biological Life Sciences. | Worldwide |
| Aniline | Aniline appears as a yellowish to brownish oily liquid with a musty fishy odor. Melting point -6°C; boiling point 184°C; flash point 158°F. Denser than water (8.5 lb / gal) and slightly soluble in water. Vapors heavier than air. Toxic by skin absorption and inhalation. Produces toxic oxides of nitrogen during combustion. Used to manufacture other chemicals, especially dyes, photographic chemicals, agricultural chemicals and others.;Liquid; PelletsLargeCrystals; Liquid; COLOURLESS OILY LIQUID WITH CHARACTERISTIC ODOUR. TURNS BROWN ON EXPOSURE TO AIR OR LIGHT.;Colorless to brown, oily liquid with an aromatic amine-like odor.;Colorless to brown, oily liquid with an aromatic amine-like odor. [Note: A solid below 21°F.]. Group: Polymers. Product ID: aniline. Molecular formula: 93.13g/mol. Mole weight: C6H7N;C6H5NH2;C6H7N. C1=CC=C(C=C1)N. InChI=1S / C6H7N / c7-6-4-2-1-3-5-6 / h1-5H, 7H2. PAYRUJLWNCNPSJ-UHFFFAOYSA-N. | |
| aralkylamine dehydrogenase (azurin) | Phenazine methosulfate can act as acceptor. Acts on aromatic amines and, more slowly, on some long-chain aliphatic amines, but not on methylamine or ethylamine. Group: Enzymes. Synonyms: aromatic amine dehydrogenase; arylamine dehydrogenase; tyramine dehydrogenase; aralkylamine:(acceptor) oxidoreductase (deaminating). Enzyme Commission Number: EC 1.4.9.2. 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-1489; aralkylamine dehydrogenase (azurin); EC 1.4.9.2; aromatic amine dehydrogenase; arylamine dehydrogenase; tyramine dehydrogenase; aralkylamine:(acceptor) oxidoreductase (deaminating). Cat No: EXWM-1489. | |
| aromatic-L-amino-acid decarboxylase | A pyridoxal-phosphate protein. The enzyme also acts on some other aromatic L-amino acids, including L-tryptophan, L-tyrosine and L-phenylalanine. Group: Enzymes. Synonyms: DOPA decarboxylase; tryptophan decarboxylase; hydroxytryptophan decarboxylase; L-DOPA decarboxylase; aromatic amino acid decarboxylase; 5-hydroxytryptophan decarboxylase; aromatic-L-amino-acid carboxy-lyase (tryptamine-forming). Enzyme Commission Number: EC 4.1.1.28. CAS No. 9042-64-2. 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-4771; aromatic-L-amino-acid decarboxylase; EC 4.1.1.28; 9042-64-2; DOPA decarboxylase; tryptophan decarboxylase; hydroxytryptophan decarboxylase; L-DOPA decarboxylase; aromatic amino acid decarboxylase; 5-hydroxytryptophan decarboxylase; aromatic-L-amino-acid carboxy-lyase (tryptamine-forming). Cat No: EXWM-4771. | |
| arylamine N-acetyltransferase | Wide specificity for aromatic amines, including serotonin; also catalyses acetyl-transfer between arylamines without CoA. Group: Enzymes. Synonyms: arylamine acetylase; β-naphthylamine N-acetyltransferase; 4-aminobiphenyl N-acetyltransferase; acetyl CoA-arylamine N-acetyltransferase; 2-naphthylamine N-acetyltransferase; arylamine acetyltransferase; indoleamine N-acetyltransferase; N-acetyltransferase (ambiguous); p-aminosalicylate N-acetyltransferase; serotonin acetyltransferase; serotonin N-acetyltransferase. Enzyme Commission Number: EC 2.3.1.5. CAS No. 9027-33-2. 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-2229; arylamine N-acetyltransferase; EC 2.3.1.5; 9027-33-2; arylamine acetylase; β-naphthylamine N-acetyltransferase; 4-aminobiphenyl N-acetyltransferase; acetyl CoA-arylamine N-acetyltransferase; 2-naphthylamine N-acetyltransferase; arylamine acetyltransferase; indoleamine N-acetyltransferase; N-acetyltransferase (ambiguous); p-aminosalicylate N-acetyltransferase; serotonin acetyltransferase; serotonin N-acetyltransferase. Cat No: EXWM-2229. | |
| Bis(2,4-diamino-5-methylphenyl)methane | It is formed by interaction of methanol and the aromatic amine 2,4-diaminotoluene. A new mutagenic compound. Group: Biochemicals. Alternative Names: 4,4'-Methylenebis[6-methyl-1,3-benzenediamine. Grades: Highly Purified. CAS No. 97-22-3. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Carbidopa Hydrate | Carbidopa Hydrate is a hydrate form of Carbidopa. Carbidopa is an aromatic-L-amino-acid decarboxylase inhibitor with an IC50 of 29 ± 2 μM. It inhibits the conversion of levodopa to dopamine. Uses: Antiparkinson agents. Synonyms: α-Methyldopahydrazine monohydrate; (S)-3-(3,4-Dihydroxyphenyl)-2-hydrazino-2-methylpropanoic acid monohydrate; N-amino-alpha-methyl-3-hydroxy-L-tyrosine monohydrate; (S)-α-Hydrazino-3,4-dihydroxy-α-methylbenzenepropanoic acid monohydrate; (-)-L-α-Hydrazino-3,4-dihydroxy-α-methylhydrocinnamic acid monohydrate; Lodosin monohydrate; Lodosyn monohydrate; MK 486 monohydrate; N-Aminomethyldopa monohydrate; (S)-(-)-Carbidopa monohydrate. Grades: ≥95%. CAS No. 38821-49-7. Molecular formula: C10H14N2O4.H2O. Mole weight: 244.25. | |
| cyclohexylamine oxidase | A flavoprotein (FAD). Some other cyclic amines can act instead of cyclohexylamine, but not simple aliphatic and aromatic amides. Group: Enzymes. Enzyme Commission Number: EC 1.4.3.12. CAS No. 63116-97-2. 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-1468; cyclohexylamine oxidase; EC 1.4.3.12; 63116-97-2. Cat No: EXWM-1468. | |
| Cytosine 99+% (HPLC) | Cytosine (C) is one of the four main bases found in DNA and RNA, along with adenine, guanine, and thymine (uracil in RNA). It is a pyrimidine derivative, with a heterocyclic aromatic ring and two substituents attached (an amine group at position 4 and a keto group at position 2). The nucleoside of cytosine is cytidine. In Watson-Crick base pairing, it forms three hydrogen bonds with guanine. Group: Biochemicals. Alternative Names: 4-Amino-2-hydroxypyrimidine; 4-Amino-2-oxo-1,2-dihydropyrimidine. Grades: Highly Purified. CAS No. 71-30-7. Pack Sizes: 25g, 100g, 250g. US Biological Life Sciences. | Worldwide |
| Dansyl chloride | Dansyl chloride is a reagent that produces stable blue or blue-green fluorescent sulfonamide adducts in the reaction of aliphatic and aromatic amines with primary amino groups, and is widely used for modified amino acids, protein sequencing and amino acid analysis [1]. Uses: Scientific research. Group: Fluorescent dye. Alternative Names: DNSCl. CAS No. 605-65-2. Pack Sizes: 1 g; 5 g; 10 g. Product ID: HY-D0017. | |
| Diphenylamine | Diphenylamine is an aromatic amine that was shown to exhibit antioxidant activities and is now used as an anti-scald agent. Group: Biochemicals. Alternative Names: N-Phenylbenzenamine; Diphenylamine; Anilinobenzene; (Phenylamino)benzene; DBA; DFA; DPA; N,N-Diphenylamine; N-Phenylaniline; N-Phenylbenzenamine; NSC 215210; Naugalube 428L; No-Scald. Grades: Highly Purified. CAS No. 122-39-4. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| Homovanillic acid | Homovanillic acid is a dopamine metabolite found to be associated with aromatic L-amino acid decarboxylase deficiency, celiac disease, growth hormone deficiency, and sepiapterin reductase deficiency. Uses: Scientific research. Group: Natural products. Alternative Names: Vanilacetic acid. CAS No. 306-08-1. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg. Product ID: HY-N0384. | |
| Homovanillic acid (Standard) | Homovanillic acid (Standard) is the analytical standard of Homovanillic acid. This product is intended for research and analytical applications. Homovanillic acid is a dopamine metabolite found to be associated with aromatic L-amino acid decarboxylase deficiency, celiac disease, growth hormone deficiency, and sepiapterin reductase deficiency. Uses: Scientific research. Group: Natural products. Alternative Names: Vanilacetic acid (Standard). CAS No. 306-08-1. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0384R. | |
| indolepyruvate ferredoxin oxidoreductase | Contains thiamine diphosphate and [4Fe-4S] clusters. Preferentially utilizes the transaminated forms of aromatic amino acids and can use phenylpyruvate and p-hydroxyphenylpyruvate as substrates. This enzyme, which is found in archaea, is a member of the 2-oxoacid oxidoreductases, a family of enzymes that oxidatively decarboxylate different 2-oxoacids to form their CoA derivatives, and are differentiated based on their substrate specificity. For examples of other members of this family, see EC 1.2.7.3, 2-oxoglutarate synthase and EC 1.2.7.7, 3-methyl-2-oxobutanoate dehydrogenase (ferredoxin). Group: Enzymes. Synonyms: 3-(indol-3-yl)pyruvate synthase (ferredoxin); IOR. Enzyme Commission Number: EC 1.2.7.8. CAS No. 158886-06-7. 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-1231; indolepyruvate ferredoxin oxidoreductase; EC 1.2.7.8; 158886-06-7; 3-(indol-3-yl)pyruvate synthase (ferredoxin); IOR. Cat No: EXWM-1231. | |
| MeIQx | MeIQx, a dietary aromatic amine, is mutagenic compound could be isolated from present in fried beef and beef extracts. MeIQx binds covalently to hemoglobin. MeIQx induces liver tumors [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 2-Amino-3,8-dimethylimidazo[4,5-f]quinoxaline-2. CAS No. 77500-04-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-W355129. | |
| methionine transaminase | The enzyme is most active with L-methionine. It participates in the L-methionine salvage pathway from S-methyl-5'-thioadenosine, a by-product of polyamine biosynthesis. The enzyme from the bacterium Klebsiella pneumoniae can use several different amino acids as amino donor, with aromatic amino acids being the most effective. The enzyme from the plant Arabidopsis thaliana is also a part of the chain elongation pathway in the biosynthesis of methionine-derived glucosinolates. Group: Enzymes. Synonyms: methionine-oxo-acid transaminase. Enzyme Commission Number: EC 2.6.1.88. 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-2929; methionine transaminase; EC 2.6.1.88; methionine-oxo-acid transaminase. Cat No: EXWM-2929. | |
| methylamine dehydrogenase (amicyanin) | Contains tryptophan tryptophylquinone (TTQ) cofactor. The enzyme oxidizes aliphatic monoamines and diamines, histamine and ethanolamine, but not secondary and tertiary amines, quaternary ammonium salts or aromatic amines. Group: Enzymes. Synonyms: amine dehydrogenase; primary-amine dehydrogenase; amine: (acceptor) oxidoreductase (deaminating); primary-amine:(acceptor) oxidoreductase (deaminating). Enzyme Commission Number: EC 1.4.9.1. 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-1488; methylamine dehydrogenase (amicyanin); EC 1.4.9.1; amine dehydrogenase; primary-amine dehydrogenase; amine: (acceptor) oxidoreductase (deaminating); primary-amine:(acceptor) oxidoreductase (deaminating). Cat No: EXWM-1488. | |
| Native Laccase from White rot fungi | Laccase (Laccase E.C. 1. 10. 3. 2) is a glucoproteinase containing copper. It can catalyze phenols and its derivatives, aromatic amine and its derivatives, carboxylic acids and its derivatives, steroid hormone, biochrome, organometallic compounds and non-phenols substrate. Applications: For indigo-dye-fading technique of jean processing by using laccase and catalysis enzymes in jean-washing industry, for selectively catalyze lignin-degradation and pulp bleaching by using laccase combined medium and xylanase. it is also a new environment friendly technique in wastepaper deinking process. for chlorophenols organic compounds degradation of wastewater treatment (which in line with ph requirements of laccase). for baking. for extract sugar. it can raise color value remaining. for others using as fiberboard adhesive, hair dyeing, lacquer dyeing film formation, crosslinking agent and biological measurement. Group: Enzymes. Synonyms: Laccases; EC 1.10. CAS No. 80498-15-3. Laccase. Activity: 10,000u/ml. Stability: 6 months at 5°C, activity remain ≥90%. Increase dosage after shelf life. Appearance: Liquid. Storage: Should be stored in a cool place to avoid effect of high temperature. Source: White rot fungi. Laccases; EC 1.10.3.2; 80498-15-3; urishiol oxidase; urushiol oxidase; p-diphenol oxidase; benzenediol:oxygen oxidoreductase. Cat No: NATE-1021. | |
| Native Streptococcus faecalis L-Phenylalanine decarboxylase | In enzymology, a phenylalanine decarboxylase (EC 4.1.1.53) is an enzyme that catalyzes the chemical reaction:L-phenylalanine<-> phenylethylamine + CO2. Hence, this enzyme has one substrate, L-phenylalanine, and two products, phenylethylamine and CO2. This enzyme belongs to the family of lyases, specifically the carboxy-lyases, which cleave carbon-carbon bonds. This enzyme participates in phenylalanine metabolism. It employs one cofactor, pyridoxal phosphate. Group: Enzymes. Synonyms: phenylalanine decarboxylase; L-phenylalanine decarboxylase; aromatic L-amino acid decarboxylase; L-phenylalanine carboxy-lyase; EC 4.1.1.53; 9075-72-3. Enzyme Commission Number: EC 4.1.1.53. CAS No. 9075-72-3. L-Phenylalanine decarboxylase. Activity: > 5 units/g solid. Storage: -20°C. Form: Dried cells from which activity can be extracted. Source: Streptococcus faecalis. phenylalanine decarboxylase; L-phenylalanine decarboxylase; aromatic L-amino acid decarboxylase; L-phenylalanine carboxy-lyase; EC 4.1.1.53; 9075-72-3. Cat No: NATE-0415. | |
| Native Streptococcus faecalis L-Tyrosine Decarboxylase Apoenzyme | In enzymology, a tyrosine decarboxylase (EC 4.1.1.25) is an enzyme that catalyzes the chemical reaction:L-tyrosine<-> tyramine + CO2. Hence, this enzyme has one substrate, L-tyrosine, and two products, tyramine and carbon dioxide. This enzyme belongs to the family of lyases, specifically the carboxy-lyases, which cleave carbon-carbon bonds. This enzyme participates in tyrosine metabolism and alkaloid biosynthesis. It employs one cofactor, pyridoxal phosphate. Applications: L-tyrosine decarboxylase apoenzyme from strept oc occus faecalis has been used in a study to purify and characterize tyrosine decarboxylase and aromatic-l-amino-acid decarboxylase. l-tyrosine decarboxylase apoenzyme from strept oc occus faecalis has also been used in a study to investigate the stereospecificity of sodium borohydride reduction of tyrosine decarboxylase. Group: Enzymes. Synonyms: tyrosine decarboxylase; EC 4.1.1.25; L-tyrosine decarb. Enzyme Commission Number: EC 4.1.1.25. CAS No. 9002-9-9. L-Tyrosine Decarboxylase. Activity: <0.005 unit/mg solid (without pyridoxal 5-phosphate),> 0.05 unit/mg solid (with excess pyridoxal 5-phosphate). Storage: -20°C. Source: Streptococcus faecalis. tyrosine decarboxylase; EC 4.1.1.25; L-tyrosine decarboxylase; L-(-)-tyrosine apodecarboxylase; L-tyrosine carboxy-lyase; 9002-09-9. Cat No: NATE-0420. | |
| N-Methylpyrrolidone (NMP) | NMP, used in precision degreasing, cleaning and wiping applications in electronics, metal cleaning and painting operations, is a clear, colorless liquid with a slight amine odor. It is considered by many as a solvent that is safer, than more volatile and reactive aromatic and aliphatic solvents. Sometimes used to replace ozone depleting solvents. Versatile effective solvent in many specialty uses. Uses: Cleaning and degreasing. Alternative Names: N-Methyl-2-pyrrolidone, N-Methyl-alpha-pyrrolidone , 1-Methyl-2-pyrrolidone , NMP. Grades: Technical and Electronics Grade. CAS No. 872-50-4. Pack Sizes: 55 gallon Drums, IBC tote containers, bulk. |  USA |
| N,N-Dimethyl-1-naphthylamine | N,N-Dimethyl-1-naphthylamine is an aromatic amine and a dye. N,N-Dimethyl-1-naphthylamine can be used in nitrate reduction test [1] [2]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 86-56-6. Pack Sizes: 1 g; 5 g; 10 g. Product ID: HY-D0222. | |
| N-Succinimidyl 4- (Maleimidomethyl) cyclohexane-1-carboxylate (SMCC) | A heterobifunctional cross-linking reagent incorporating an extended spacer with amine and sulfhydryl reactivity. Typically coupled initially to molecules containing primary amine by amide bond buffered at pH 7.5 (6.5-8.5). The second coupling is specific for molecules containing free sulfhydryl by thioether linkage buffered at pH 6.8 (6.5-7.0). Useful for preparation of enzyme immunoconjugates and hapten carrier molecule conjugates. Contains 9 atom linker. An extended aliphatic spacer stabilizes the maleimide prior to coupling compared to aromatic spacers. Group: Biochemicals. Alternative Names: 4- (N-Maleimidomethyl) cyclohexane-1-carboxylic Acid N-Hydroxysuccinimide Ester; NSC 344483; SMCC. Grades: Highly Purified. CAS No. 64987-85-5. Pack Sizes: 25mg, 100mg, 250mg, 500mg. US Biological Life Sciences. | Worldwide |
| o-Toluidine Chloride | o-Toluidine Chloride is a carcinogenic and toxic aromatic amine contained in hair dye, henna and dyed hair samples. Prilocaine USP Related Compound A. Group: Biochemicals. Grades: Highly Purified. CAS No. 636-21-5. Pack Sizes: 50mg, 1g. Molecular Formula: C7H10ClN. US Biological Life Sciences. | Worldwide |
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