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| Product | Description | |
|---|---|---|
| Tertiary Butylhydroquinone | Tert-butylhydroquinone appears as white to light tan crystalline powder or a fine beige powder. Very slight aromatic odor. (NTP, 1992);DryPowder, Liquid;White crystalline solid having a characteristic odour;Solid. Group: Polymers. Product ID: 2-tert-butylbenzene-1,4-diol. Molecular formula: 166.22g/mol. Mole weight: C10H14O2;C10H14O2. CC(C)(C)C1=C(C=CC(=C1)O)O. InChI=1S/C10H14O2/c1-10(2, 3)8-6-7(11)4-5-9(8)12/h4-6, 11-12H, 1-3H3. BGNXCDMCOKJUMV-UHFFFAOYSA-N. |  |
| Tertiary Butylhydroquinone | Tertiary Butylhydroquinone Synonyms: TBHQ CAS: 1948-330 Packing: Bag. Categories: tert-Butylhydroquinone (TBHQ). |  New Jersey NJ |
| Dodecyl tertiary amine | Heterocyclic Organic Compound. CAS No. 112-18-8. Molecular formula: (CH3)2NC12H25. Catalog: ACM112188. |  |
| Lithium tertiary butoxide | Lithium tertiary butoxide. Group: Biochemicals. Grades: Highly Purified. CAS No. 1907-33-1. Pack Sizes: 5g, 10g, 25g. US Biological Life Sciences. |  Worldwide |
| Methyl Tertiary Butyl Phenyl Acetate Para | Methyl Tertiary Butyl Phenyl Acetate Para. CAS No. 3549-23-3. FEMA No. 2690. Kosher: Y. VIGON Item # 502662. Categories: Speciality Ingrdients Suppliers, Flavors, Fragrances, Perfumers. |  America & Internationally |
| Para Tertiary Butylphenol Formaldehyde Resin | Para Tertiary Butylphenol Formaldehyde Resin is a phenol-formaldehyde resin found in commercial adhesives, and in particular in adhesives used to bond leather and rubber. Synonyms: p-tert-butylphenol-formaldehyde resin; PTBP-FR; PTBPFR; 4-(1,1-dimethylethyl) phenol; PTBP Formaldehyde. |  |
| Toluene-4-sulfonic acid 2-tertiary-butoxyethyl ester | Heterocyclic Organic Compound. Alternative Names: TOLUENE-4-SULFONIC ACID 2-TERT-BUTOXY ETHYL ESTER. CAS No. 108366-80-9. Molecular formula: C13H20O4S. Mole weight: 272.361. Purity: 0.96. IUPACName: Toluene-4-sulfonic acid 2-tertiary-butoxy ethyl ester. Catalog: ACM108366809. | |
| 1, 1'-Bis (diisopropylphosphino)ferrocene | Ruthenium- catalyzed hydrohydroxyalkylation of 1,1-disubstituted allenes Ligand for palladium-catalyzed aminocarbonylation of Pyridyl Tosylates by means of ex situ generation of CO. Pd-catalyzed carbonylative ?-arylation of ketones with aryl iodides Ligand for palladium-catalyzed alkoxycarbonylation of aryl bromides for the preparation of tertiary esters Ligand for stereoselective palladium-catalyzed decarboxylative allylation ß-C-glycosylation Ligand for ruthenium-catalyzed C-C coupling reactions of fluorinated alcohols with allenes. Ligand for cobalt-catalyzed intermolecular formal hydroacylation reaction of olefins using N-3-picolin-2-yl aldimines as aldehyde equivalents. Group: Organic phosphine compounds. Alternative Names: 1,1-BIS(DIISOPROPYLPHOSPHINO)FERROCENE. CAS No. 97239-80-0. Molecular formula: C22H36FeP2. Mole weight: 418.32. Appearance: Orange-yellow powder. Purity: 0.98. IUPACName: 1,1-Bis(diisopropylphosphino)ferrocene. Catalog: ACM97239800. | |
| 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-Boc-pyrrolidine-3-carboxaldehyde | 1-Boc-pyrrolidine-3-carboxaldehyde is used in the preparation of tertiary amines as agonists of the nuclear hormone receptor Rev-erbα. Group: Biochemicals. Grades: Highly Purified. CAS No. 59379-02-1. Pack Sizes: 10mg, 100mg. Molecular Formula: C10H17NO3, Molecular Weight: 199.25. US Biological Life Sciences. | Worldwide |
| [1- (Methylamino) cyclohexyl]methanol | [1- (Methylamino) cyclohexyl]methanol is used in the synthetic preparation of tertiary amino alcohol compounds. Group: Biochemicals. Grades: Highly Purified. CAS No. 1094071-92-7. Pack Sizes: 250mg, 1g. Molecular Formula: C8H17NO, Molecular Weight: 143.229999999999. US Biological Life Sciences. | Worldwide |
| 1- methyl cyclopropanecarboxylic Acid Ethyl Ester | 1- methyl cyclopropanecarboxylic Acid Ethyl Ester is used to prepare secondary and tertiary amides directly with sodium diethyl diamidoaluminate as the catalyst. It is also used to study trimethylaluminium mediated amide bond formation in a continuous flow microreactor. Group: Biochemicals. Grades: Highly Purified. CAS No. 71441-76-4. Pack Sizes: 1g, 10g. Molecular Formula: C7H12O2, Molecular Weight: 128.169999999999. US Biological Life Sciences. | Worldwide |
| (1S,2S)-(+)-[1,2-Cyclohexanediamino-N,N'-bis(3,5-di-t-butylsalicylidene)]chromium(III) chloride | Catalyst for the asymmetric ring-opening of meso-epoxides and for the kinetic resolution of terminal epoxides. Precatalyst for asymmetric Diels-Alder and hetero Diels-Alder reactions. Catalyst for copolymerization of CO2 and epoxides. Catalyst for enantioselective alkylation of tributyltin enolates. Enantioselective addition of Me2Zn to aldehydes. Enantioselective intramolecular addition of tertiary enamides to ketones. Asymmetric iodocyclization. Catalytic intermolecular linear allylic C-H animation. Cocatalyst for enantioselective ring opening of epoxides with fluoride. Group: Heterocyclic organic compound. Alternative Names: SCHEMBL2189792;219143-92-7;(S,S)-N,N -Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminochromium(III) chloride. CAS No. 219143-92-7. Molecular formula: C36H54ClCrN2O2-. Mole weight: 634.286g/mol. IUPACName: chromium; 2, 4-ditert-butyl-6- [ [ (1S, 2S) -2- [ (3, 5-ditert-butyl-2-hydroxyphenyl) methylideneamino] cyclohexyl] iminomethyl] phenol; chloride. Canonical SMILES: CC (C) (C)C1=CC (=C (C (=C1)C=NC2CCCCC2N=CC3=CC (=CC (=C3O)C (C) (C)C)C (C) (C)C)O)C (C) (C)C. [Cl-]. [Cr]. ECNumber: 606-861-4. Catalog: ACM219143927. | |
| 2,2,2-Trichloroethyl Chloroformate | 2,2,2-Trichloroethyl Chloroformate is a general reagent for the demethylation of tertiary methylamines. It is used as a reagent in the synthesis of a series of piperazine ureas as fatty acid amide hydrolase inhibitors and analgesics. Also used as a reagent in the synthesis of pyrazolo[3,4-d]pyrimidine derivatives as GPR119 agonists. Group: Biochemicals. Grades: Highly Purified. CAS No. 17341-93-4. Pack Sizes: 1g, 10 g. Molecular Formula: C3H2Cl4O2. US Biological Life Sciences. | Worldwide |
| 2,5-Di-tert-butylhydroquinone | PelletsLargeCrystals. Group: Plastic additives. Alternative Names: Di-Tertiary butylhydroquinone. CAS No. 88-58-4. Product ID: 2,5-Ditert-butylbenzene-1,4-diol. Molecular formula: 222.32. Mole weight: C14H22O2. CC(C)(C)C1=CC(=C(C=C1O)C(C)(C)C)O. InChI=1S/C14H22O2/c1-13(2, 3)9-7-12(16)10(8-11(9)15)14(4, 5)6/h7-8, 15-16H, 1-6H3. JZODKRWQWUWGCD-UHFFFAOYSA-N. 98%+. | |
| 2-(Bromomethyl)-5-(trifluoromethyl)furan | 2-(Bromomethyl)-5-(trifluoromethyl)furan is an intermediate used to prepare tertiary sulfonamides as liver X receptor antagonists. It is also used to synthesize hydantoin based inhibitors of MMP13 with potential use in osteoarthritis. Group: Biochemicals. Grades: Highly Purified. CAS No. 17515-77-4. Pack Sizes: 250mg, 1g. Molecular Formula: C6H4BrF3O. US Biological Life Sciences. | Worldwide |
| 2-Methyl-2-pentanol | 2-Methyl-2-pentanol is a perfluorinated tertiary alcohol that is commonly found in fruits when they reach their maturation stages. Group: Biochemicals. Grades: Highly Purified. CAS No. 590-36-3. Pack Sizes: 2.5g, 10 g. Molecular Formula: C6H14O, Molecular Weight: 102.17. US Biological Life Sciences. | Worldwide |
| 2-Phenyl-1,2,3,4-tetrahydroisoquinoline | 2-Phenyl-1,2,3,4-tetrahydroisoquinoline is a reactant that is used in acetic acid promoted metal-free aerobic carbon-carbon bond forming reactions at α-position of tertiary amines. Group: Biochemicals. Grades: Highly Purified. CAS No. 3340-78-1. Pack Sizes: 500mg, 5g. Molecular Formula: C15H15N. US Biological Life Sciences. | Worldwide |
| 3-Diethylamino-1-propanol | 3-Diethylamino-1-propanol is an tertiary amine compound with anticonvulsant activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 622-93-5. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-W010383. |  |
| 3-Fluoroanisole | 3-Fluoroanisole is used in the preparation of tertiary benzylic nitriles. Group: Biochemicals. Grades: Highly Purified. CAS No. 456-49-5. Pack Sizes: 10g, 50g, 100g. Molecular Formula: C?H?FO, Molecular Weight: 126.13. US Biological Life Sciences. | Worldwide |
| 4-Bromo-2-methyl-2-butanol | 4-Bromo-2-methyl-2-butanol is a brominated tertiary alcohol used as a reagent in the preparation of vitamin D3 analogues. Group: Biochemicals. Alternative Names: 4-Bromo-2-hydroxy-2-methylbutane. Grades: Highly Purified. CAS No. 35979-69-2. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| 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 |
| 5-Vinyl-UTP | 5-Vinyl-UTP is a vital tool in the biomedical industry used for the research and development of modified RNA molecules. This compound is commonly employed in research to investigate RNA tertiary structures, RNA-protein interactions and RNA enzymatic activities. Furthermore, 5-Vinyl-UTP facilitates the study of RNA-related diseases and the development of potential RNA-based therapeutics for a range of disorders. Grades: ≥ 95% by HPLC. Molecular formula: C11H17N2O15P3 (free acid). Mole weight: 510.18 (free acid). | |
| (+)-Aeroplysinin-1 | (+)-Aeroplysinin-1 is a metabolite originally isolated from the marine sponge V. aerophoba with diverse biological activity. It is a tertiary alcohol. Synonyms: NSC 170364; Aeroplysinin 1; (+)-shy-Aeroplysinin-1; (1S,6R)-3,5-Dibromo-1,6-dihydroxy-4-methoxy-2,4-cyclohexadiene-1-acetonitrile; Aeroplysinin; Aeroplysinin I; (1S-trans)-3,5-dibromo-1,6-dihydroxy-4-methoxy-2,4-cyclohexadiene-1-acetonitrile. Grades: ≥95%. CAS No. 28656-91-9. Molecular formula: C9H9Br2NO3. Mole weight: 338.98. | |
| Alcohol Soluble Polyamide Resin ALFA12 | This alcohol soluble grade polyamide resin is made of trimeric acid and tertiary amine through condensation reaction. Uses: Mainly used for manufacturing gravure plastic printing ink, paper ink and hot melt binder, etc. Group: Alcohol soluble polyamide resins. | |
| Alcohol Soluble Polyamide Resin ALFA13 | This alcohol soluble grade polyamide resin is made of trimeric acid and tertiary amine through condensation reaction. Uses: Mainly used for manufacturing gravure plastic printing ink, paper ink and hot melt binder, etc. Group: Alcohol soluble polyamide resins. | |
| Alcohol Soluble Polyamide Resin ALFA14 | This alcohol soluble grade polyamide resin is made of trimeric acid and tertiary amine through condensation reaction. Uses: Mainly used for manufacturing gravure plastic printing ink, paper ink and hot melt binder, etc. Group: Alcohol soluble polyamide resins. | |
| Alcohol Soluble Polyamide Resin ALFA15 | This alcohol soluble grade polyamide resin is made of trimeric acid and tertiary amine through condensation reaction. Uses: Mainly used for manufacturing gravure plastic printing ink, paper ink and hot melt binder, etc. Group: Alcohol soluble polyamide resins. | |
| amine N-methyltransferase | An enzyme of very broad specificity; many primary, secondary and tertiary amines can act as acceptors, including tryptamine, aniline, nicotine and a variety of drugs and other xenobiotics. Group: Enzymes. Synonyms: nicotine N-methyltransferase; tryptamine N-methyltransferase; arylamine N-methyltransferase; tryptamine methyltransferase. Enzyme Commission Number: EC 2.1.1.49. CAS No. 51377-47-0, 111694-10-1. 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-1952; amine N-methyltransferase; EC 2.1.1.49; 51377-47-0, 111694-10-1; nicotine N-methyltransferase; tryptamine N-methyltransferase; arylamine N-methyltransferase; tryptamine methyltransferase. Cat No: EXWM-1952. |  |
| 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%. | |
| Benzene Soluble Polyamide Resin ALFA10 | This benzene-soluble grade polyamide resin is made from trimeric acid and tertiary amine by condensation reaction. Uses: Mainly used for manufacturing gravure plastic printing ink, paper ink and hot melt binder, etc. Group: Benzene soluble polyamide resins. | |
| Benzene Soluble Polyamide Resin ALFA11 | This benzene-soluble grade polyamide resin is made from trimeric acid and tertiary amine by condensation reaction. Uses: Mainly used for manufacturing gravure plastic printing ink, paper ink and hot melt binder, etc. Group: Benzene soluble polyamide resins. | |
| Benzene Soluble Polyamide Resin ALFA12 | This benzene-soluble grade polyamide resin is made from trimeric acid and tertiary amine by condensation reaction. Uses: Mainly used for manufacturing gravure plastic printing ink, paper ink and hot melt binder, etc. Group: Benzene soluble polyamide resins. | |
| Benzene Soluble Polyamide Resin ALFA13 | This benzene-soluble grade polyamide resin is made from trimeric acid and tertiary amine by condensation reaction. Uses: Mainly used for manufacturing gravure plastic printing ink, paper ink and hot melt binder, etc. Group: Benzene soluble polyamide resins. | |
| Benzethonium Chloride | Benzethonium Chloride. CAS No. 121-54-0. Product ID: PE-0634. Molecular formula: C27H42ClNO2. Mole weight: 448.1. Category: Antibacterial Agents; Preservative; Disinfectant. Product Keywords: Excipients for Liquid Dosage Form; Surfactant Excipients; PE-0634; Benzethonium Chloride; Antibacterial Agents; Preservative; Disinfectant; C27H42ClNO2; 121-54-0. UNII: PH41D05744. Chemical Name: N, N-Dimethyl-N-[2-[2-[4-(1, 1, 3, 3-tetramethylbutyl) phenoxy]ethoxy]eyhyl]benzene- methanaminium chloride. Grade: Pharmceutical Excipients. Administration route: AURICULAR (OTIC); INTRAMUSCULAR; INTRAVENOUS; OPHTHALMIC; Topical. Dosage Form: Solution; Injection; Soultion/drops; Cream. Stability and Storage Conditions: Benzoxolium chloride is stable and an aqueous solution can be autoclaved. Store bulk apis air-tight in a cool, dry and dark place. Source and Preparation: 2-[2-[4-(1, 1, 3, 3-tetramethylbutyl) phenoxyl] ethoxy] ethyl chloride was synthesized by condensation of P-diisobutylphenol with β, β '-dichlorodiethyl ether under alkaline catalysis. The product is then converted into the corresponding tertiary amine by alkaline dimethylamine. After distillation and purification, it is dissolved in an appropriate amount of organic solvent and treated with benzyl chloride. The product is precipitated. Applications: Benzoxonium chloride is a quaternary ammonium compound used as an antimicrobial agent in pharmaceutical |  |
| Benzhexol HCl | Benzhexol HCl is an anticholinergic tertiary amine used to treat parkinsonism and the extrapyramidal side effects of anti-psychotic drugs. Uses: Anticholinergic tertiary amine. Synonyms: Trihexyphenidyl Hydrochloride; 1-cyclohexyl-1-phenyl-3-piperidin-1-ylpropan-1-ol; hydrochloride; Trihexyphenidylhydrochloride; Benzhexolhydrochloride; Artane; 52-49-3. Grades: ≥98%. CAS No. 52-49-3. Molecular formula: C20H32ClNO. Mole weight: 337.94. | |
| Betamethasone Acetate | Betamethasone acetate is an acetate ester, a steroid ester, a fluorinated steroid, a 17alpha-hydroxy steroid, a 20-oxo steroid, an 11beta-hydroxy steroid, a 3-oxo-Delta(1),Delta(4)-steroid and a tertiary alpha-hydroxy ketone. It is functionally related to a betamethasone. CAS No. 987-24-6. Product ID: PAP-0075. Molecular formula: C24H31FO6. Category: Hormone drug. Product Keywords: Hormone Series; Betamethasone Acetate; PAP-0075; Hormone drug; C24H31FO6; 987-24-6. Standard: BP/USP/EP. Color: White to Off-White. EC Number: 213-578-6. Physical State: neat. Solubility: Practically insoluble in water, freely soluble in acetone, soluble in ethanol (96 per cent) and in methylene chloride. It shows polymorphism (5.9). Storage: Refrigerator. Applications: Betamethasone acetate is a synthetic glucocorticoid corticosteroid and a corticosteroid ester. It is the 21-acetate ester of betamethasone. Boiling Point: 579.4±50.0 °C(Predicted). Melting Point: 200-220°C (dec.). Density: 1.0932 (rough estimate). Product Description: Betamethasone acetate is a synthetic glucocorticoid corticosteroid and a corticosteroid ester. It is the 21-acetate ester of betamethasone. | |
| bleomycin hydrolase | The molecule is a homohexamer in which the monomers have a papain-like tertiary structure (in peptidase family C1). The active sites are on the walls of a central channel through the molecule, and access of substrate molecules to them is obstructed by this and by the C-terminus of each polypeptide chain. Bleomycin can scarcely be the natural substrate, and there are reports of limited endopeptidase activity. Known from bacteria as well as eukaryotic organisms. Hydrolase H from chicken muscle has many similarities to bleomycin hydrolase, but hydrolyses Ph-CO-Arg-2-naphthylamine as well as aminopeptidase substrates. Group: Enzymes. Synonyms: aminopeptidase C (Lactococcus lactis). Enzyme Commission Number: EC 3.4.22.40. CAS No. 53096-17-6. 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-4215; bleomycin hydrolase; EC 3.4.22.40; 53096-17-6; aminopeptidase C (Lactococcus lactis). Cat No: EXWM-4215. | |
| Boc-L-Ile-CHN2 | Heterocyclic Organic Compound. Alternative Names: BOC-L-ILE-CHN2; N-ALPHA-T-BUTYLOXYCARBONYL-L-ISOLEUCINYL-DIAZOMETHANE; (3S,4S)-N-TERTIARY-BUTOXYCARBONYLISOLEUCINYL DIAZOMETHANE. CAS No. 114645-19-1. Molecular formula: C12H21N3O3. Mole weight: 255.32. Purity: 0.96. IUPACName: [(3S,4S)-N-tert-Butoxycarbonyl-L-isoleucyl]diazomethane. Catalog: ACM114645191. | |
| Calcium phosphate monobasic monohydrate | Calcium phosphate monobasic monohydrate. Synonyms: Calcium bis(dihydrogenphosphate) monohydrate, Calcium dihydrogenphosphate monohydrate, Primary calcium phosphate monohydrate. CAS No. 10031-30-8. Pack Sizes: 100, 500 g, 1 kg. Product ID: CDC10-0009. Molecular formula: CaH7O5P. Category: Cosmetic Chemical Abrasives. Product Keywords: Cosmetic Ingredients; Cosmetic Chemical Abrasives; Calcium phosphate monobasic monohydrate; CDC10-0009; 10031-30-8; CaH7O5P; Calcium bis(dihydrogenphosphate) monohydrate, Calcium dihydrogenphosphate monohydrate, Primary calcium phosphate monohydrate; 231-837-1; MFCD00149602; 10031-30-8. Grade: purum p.a. Purity: ≥85% (KT). EC Number: 231-837-1. Physical State: Powder or crystals. Quality Level: 200. Storage: Store at room temperature. Boiling Point: 203°C. Melting Point: N/A. Product Description: Calcium phosphate monobasic monohydrate is mainly used in the manufacture of fertilizers and as an acidulant in food industry. Aqueous solution of calcium phosphate monobasic monohydrate (MCPM) mixed with α-tertiary calcium phosphate forms dicalcium phosphate dihydrate cement. It is also used in composing brushite cement. | |
| Carbonylchlorobis (triphenylphosphine)iridium (I) | Catalyst for the intramolecular carbonylative [2+2+1] cycloaddition of allenynes. Catalyst for the selective hydrogenation of myrcene. Catalyst for silylation of ortho-functionalized aryl halides with hydrosilanes. Catalyst for synthesis of aldenamines from carboxamides by silane-reduction/dehydration under mild conditions. Hydrogen atom transfer catalyst for radical cyclizations. Complex for photocatalytic alkane dehydrogenation. Catalyst for chemoselective reductive nucleophilic addition to N-methoxyamides. Catalyst for chemoselective reductive alkynylation of tertiary amides. Group: Iridium series of catalysts. Alternative Names: Bis(triphenylphosphine)iridium(I) carbonyl chloride. CAS No. 14871-41-1. Molecular formula: C37H32ClIrOP2. Mole weight: 782.3. Appearance: Crystal. Purity: 0.99. IUPACName: formaldehyde; iridium; triphenylphosphane; chloride. Canonical SMILES: C=O. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. [Cl-]. [Ir]. ECNumber: 238-941-6. Catalog: ACM14871411-1. | |
| Cobalt Hexamine Chloride | Hexaamminecobalt(III) chloride is used in X-ray crystallography and NMR. It is useful in DNA condensation studies. It is suitable for induction of transitions of DNA from B to A or Z forms, induction of nucleic acid crystal growth, stabilization of tertiary tRNA interactions, preparation of ligation buffer. Group: Biochemicals. Alternative Names: Hexammine cobalt(III) chloride; Cobalt hexammine trichloride, Hexaamminecobalt trichloride. Grades: Highly Purified. CAS No. 10534-89-1. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: [Co(NH3)6]Cl3, Molecular Weight: 267.48. US Biological Life Sciences. | Worldwide |
| Cyclopentaneethanol | Cyclopentaneethanol is used in the prepartion of phenylalanine derivatives for incorporation into peptides as CD4 mimetic miniproteins interacting with HIV-1 surface glycoprotein. It is also used in the preparation of tertiary amine muscarinic receptor antagonists applied towards the treatment of chronic obstructive pulmonary disease. Group: Biochemicals. Alternative Names: 2-Cyclopentaneethanol; 2-Cyclopentylethanol; 2-Cyclopentylethyl Alcohol. Grades: Highly Purified. CAS No. 766-00-7. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| D-Allylglycine | A new chiral glycine equivalent; used for the preparation of enantiomerically pure α-tertiary and α-quaternary α-amino acids. A. Group: Biochemicals. Alternative Names: (2R)-2-Amino-4-pentenoic Acid; (+)-Allylglycine; (R)-2-Amino-4-pentenoic Acid; (R)-Allylglycine; D-α-Allylglycine; D-2-Amino-4-pentenoic Acid. Grades: Highly Purified. CAS No. 54594-06-8. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| diamine oxidase | A group of enzymes that oxidize diamines, such as histamine, and also some primary monoamines but have little or no activity towards secondary and tertiary amines. They are copper quinoproteins (2,4,5-trihydroxyphenylalanine quinone) and, like EC 1.4.3.21 (primary-amine oxidase) but unlike EC 1.4.3.4 (monoamine oxidase), they are sensitive to inhibition by carbonyl-group reagents, such as semicarbazide. Group: Enzymes. Synonyms: amine oxidase (ambiguous); amine oxidase (copper-containing) (ambiguous); CAO (ambiguous); Cu-containing amine oxidase (ambiguous); copper amine oxidase (ambiguous); diamine oxidase (ambiguous); diamino oxhydrase (ambiguous); histaminase; histamine deaminase (incorrect); semicarbazide-sensitive amine oxidase (incorrect); SSAO (incorrect). Enzyme Commission Number: EC 1.4.3.22. 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-1477; diamine oxidase; EC 1.4.3.22; amine oxidase (ambiguous); amine oxidase (copper-containing) (ambiguous); CAO (ambiguous); Cu-containing amine oxidase (ambiguous); copper amine oxidase (ambiguous); diamine oxidase (ambiguous); diamino oxhydrase (ambiguous); histaminase; histamine deaminase (incorrect); semicarbazide-sensitive amine oxidase (incorrect); SSAO (incorrect). Cat No: EXWM-1477. | |
| D,L-Trihexyphenidyl, Hydrochloride (a-Cyclohexyl-a-phenyl-1-piperidinepropanol, HCl, Artane) | Artane is an anticholinergic tertiary amine that can. Group: Biochemicals. Alternative Names: a-Cyclohexyl-a-phenyl-1-piperidinepropanol, HCl, Artane. Grades: Highly Purified. CAS No. 58947-95-8. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| Esterase from Bacillus subtilis, Recombinant | An esterase is a hydrolase that splits esters into acids and alcohols. Applications: Esterase, from bacillus subtilis, may be used in protein engineering research as well as to study the kinetic resolution of acetates of arylaliphatic tertiary alcohols. this product is recombinant and expressed in e. coli (> 10 units/mg). Group: Enzymes. Synonyms: EC 3.1.1.1; ali-esterase; B-esterase; monobutyrase; cocaine esterase; procaine esterase; methylbutyrase; vitamin A esterase; butyryl esterase; carboxyesterase; carboxylate esterase; carboxylic esterase; methylbutyrate esterase; triacet. Enzyme Commission Number: EC 3.1.1.1. CAS No. 9016-18-6. Esterase. Activity: Type I, > 10 units/mg; Type II, > 0.8 units/mg. Storage: -20°C. Source: E. coli. Species: Bacillus subtilis. EC 3.1.1.1; ali-esterase; B-esterase; monobutyrase; cocaine esterase; procaine esterase; methylbutyrase; vitamin A esterase; butyryl esterase; carboxyesterase; carboxylate esterase; carboxylic esterase; methylbutyrate esterase; triacetin esterase; carboxyl ester hydrolase; butyrate esterase; methylbutyrase; α-carboxylesterase; propionyl esterase; nonspecific carboxylesterase; esterase D; esterase B; esterase A; serine esterase; carboxylic acid esterase; cocaine esterase; 9016-18-6. Pack: Bottomless glass bottle. Contents are inside inserted fused cone. Cat No: NATE-0242. | |
| flavin-containing monooxygenase | A flavoprotein. A broad spectrum monooxygenase that accepts substrates as diverse as hydrazines, phosphines, boron-containing compounds, sulfides, selenides, iodide, as well as primary, secondary and tertiary amines. This enzyme is distinct from other monooxygenases in that the enzyme forms a relatively stable hydroperoxy flavin intermediate. This microsomal enzyme generally converts nucleophilic heteroatom-containing chemicals and drugs into harmless, readily excreted metabolites. For example, N-oxygenation is largely responsible for the detoxification of the dopaminergic neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). Group: Enzymes. Synonyms: dimethylanilin...CAS No. 37256-73-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0887; flavin-containing monooxygenase; EC 1.14.13.8; 37256-73-8; dimethylaniline oxidase; dimethylaniline N-oxidase; FAD-containing monooxygenase; N,N-dimethylaniline monooxygenase; DMA oxidase; flavin mixed function oxidase; Ziegler's enzyme; mixed-function amine oxidase; FMO; FMO-I; FMO-II; FMO1; FMO2; FMO3; FMO4; FMO5; flavin monooxygenase; methylphenyltetrahydropyridine N-monooxygenase; 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine:oxygen N-oxidoreductase; dimethylaniline monooxygenase (N-oxide-forming). Cat No: EXWM-0887. | |
| Fmoc-Sec(pMeOBzl)-OH | Building block for the introduction of selenocysteine during Fmoc SPPS. Selenocysteine derivatives can undergo enantiomerization during coupling and can form dehydroalanine and β-piperidinylalanine containing side products during subsequent chain elongation. Therefore, activation methods, such as HBTU or PyBOP which involve the addition of a tertiary, base should be avoided for addition of the Sec and all subsequent residues. Cleavage and side-chain deprotection of Sec-containing peptides can be effected using tFA-m-cresol-thioanisole-EDT-water (80:5:5:5:5) or TFA-water-DCM-TIS (89:5:51) at 4 °C. As the Se-pMeOBzl bond is stable to TFA, these methods result in the formation of the corresponding Sev(pMeOBzl) peptide. Peptides containing two Sec(pMeOBzl) residues can be oxidized directly to the corresponding selenocystinyl peptides by treatment with 5-10% DMSO in TFA. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Sec(pMeOBzl)-OH, Fmoc-Sec(Mob)-OH, Fmoc-S-4-methoxybenzyl selenocysteine. CAS No. 150308-80-8. Molecular formula: C26H25NO5Se. Mole weight: 510.44. Catalog: ACM150308808. | |
| H-Allyl-D-glycine | . Uses: A new chiral glycine equivalent; used for the preparation of enantiomerically pure α-tertiary and α-quaternary α-amino acids. a bacillus spore germination alanine analog. Synonyms: D-Gly(allyl)-OH; (R)-2-Amino-4-pentenoic acid. Grades: ≥ 98% (HPLC). CAS No. 54594-06-8. Molecular formula: C5H9NO2. Mole weight: 115.14. | |
| Imipramine | Imipramine is an orally active tertiary amine tricyclic antidepressant. Imipramine is a Fascin1 inhibitor with antitumor activities. Imipramine also inhibits serotonin transporter with an IC 50 value of 32 nM. Imipramine stimulates U-87MG glioma cells autophagy and induces HL-60 cell apoptosis. Imipramine shows neuroprotective and immunomodulatory effects [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. CAS No. 50-49-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B1490A. | |
| Imipramine-d4 hydrochloride | Imipramine-d 4 (hydrochloride) is the deuterium labeled Imipramine hydrochloride. Imipramine hydrochloride is an orally active tertiary amine tricyclic antidepressant. Imipramine hydrochloride is a Fascin1 inhibitor with antitumor activities. Imipramine hydrochloride also inhibits serotonin transporter with an IC50 value of 32 nM. Imipramine hydrochloride stimulates U-87MG glioma cells autophagy and induces HL-60 cell apoptosis. Imipramine hydrochloride shows neuroprotective and immunomodulatory effects[1][2][3][4][5][6]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 61361-33-9. Pack Sizes: 1 mg. Product ID: HY-B1490S. | |
| Imipramine hydrochloride | Imipramine hydrochloride is an orally active tertiary amine tricyclic antidepressant. Imipramine hydrochloride is a Fascin1 inhibitor with antitumor activities. Imipramine hydrochloride also inhibits serotonin transporter with an IC 50 value of 32 nM. Imipramine hydrochloride stimulates U-87MG glioma cells autophagy and induces HL-60 cell apoptosis. Imipramine hydrochloride shows neuroprotective and immunomodulatory effects [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. CAS No. 113-52-0. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1490. | |
| (l)-2-Diazoacetyl-pyrrolidine-1-carboxylic acid tert-butyl ester | Heterocyclic Organic Compound. Alternative Names: (L)-2-DIAZOACETYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER;(L)-2-Diazoacetyl-pyrrolidine-1-carboxylic acid tertiary-butyl ester. CAS No. 101130-03-4. Molecular formula: C11H17N3O3. Mole weight: 239.27. Catalog: ACM101130034. | |
| Lipase A from Candida Antarctica, Recombinant | Lipase A from Candida Antarctica catalyzes hydrolysis of tertiary alcohols to form glycerol and fatty acids and shows selectivity for the N-acylation of β-amino esters. Group: Enzymes. Synonyms: EC 3.1.1.3; lipase; triglyceride lipase; tributyrase; butyrinase; glycerol ester hydrolase; tributyrinase; Tween hydrolase; steapsin; triacetinase; tributyrin esterase; Tweenase; amno N-AP; Takedo 1969-4-9; Meito . Enzyme Commission Number: EC 3.1.1.3. CAS No. 9001-62-1. Lipase. Activity: ~2 units/mg. Storage: 2-8°C. Form: powder; beige. Source: Aspergillus oryzae. Species: Candida Antarctica. EC 3.1.1.3; lipase; triglyceride lipase; tributyrase; butyrinase; glycerol ester hydrolase; tributyrinase; Tween hydrolase; steapsin; triacetinase; tributyrin esterase; Tweenase; amno N-AP; Takedo 1969-4-9; Meito MY 30; Tweenesterase; GA 56; capalase L; triglyceride hydrolase; triolein hydrolase; tween-hydrolyzing esterase; amano CE; cacordase; triglyceridase; triacylglycerol ester hydrolase; amano P; amano AP; PPL; glycerol-ester hydrolase; GEH; meito Sangyo OF lipase; hepatic lipase; lipazin; post-heparin plasma protamine-resistant lipase; salt-resistant post-heparin lipase; heparin releasable hepatic lipase; amano CES; amano B; tributyrase; triglyceride lipase; liver lipase; hepatic monoacylglycerol acyltransferase; 9001-62-1. Cat No: NATE-0397. | |
| (+)-Longifolene | (+)-Longifolene is a sesquiterpenoid and a metabolite in rabbits. (+)-Longifolen is converted to primary, secondary or tertiary alcohols in rabbits, among which the primary alcohol is predominant [1]. Uses: Scientific research. Group: Natural products. CAS No. 475-20-7. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-N6662. | |
| L-peptidase | Best known from foot-and-mouth disease virus, but occurs in other aphthoviruses and cardioviruses. Destruction of initiation factor eIF-4G has the effect of shutting off host-cell protein synthesis while allowing synthesis of viral proteins to continue. The tertiary structure reveals a distant relationship to papain and, consistent with this, compound E-64 is inhibitory. Type example of peptidase family C28. Group: Enzymes. Enzyme Commission Number: EC 3.4.22.46. 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-4221; L-peptidase; EC 3.4.22.46. Cat No: EXWM-4221. | |
| 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. | |
| monoamine oxidase | A mitochondrial outer-membrane flavoprotein (FAD) that catalyses the oxidative deamination of neurotransmitters and biogenic amines. Acts on primary amines, and also on some secondary and tertiary amines. It differs from EC 1.4.3.21, primary-amine oxidase as it can oxidize secondary and tertiary amines but not methylamine. This enzyme is inhibited byacetylenic compounds such as chlorgyline, 1-deprenyl and pargyline but, unlike EC 1.4.3.21 and EC 1.4.3.22 (diamine oxidase), it is not inhibited by semicarbazide. Group: Enzymes. Synonyms: adrenalin oxidase; adrenaline oxidase; amine oxidase (ambiguous); amine oxidase (flavin-containing); amine:oxygen ox. Enzyme Commission Number: EC 1.4.3.4. CAS No. 9001-66-5. Monoamine Oxidase. 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-1481; monoamine oxidase; EC 1.4.3.4; 9001-66-5; adrenalin oxidase; adrenaline oxidase; amine oxidase (ambiguous); amine oxidase (flavin-containing); amine:oxygen oxidoreductase (deaminating) (flavin-containing); epinephrine oxidase; MAO; MAO A; MAO B; MAO-A; MAO-B; monoamine oxidase A; monoamine oxidase B; monoamine:O2 oxidoreductase (deaminating); polyamine oxidase (ambiguous); serotonin deaminase; spermidine oxidase (ambiguous); spermine oxidase (ambiguous); tyraminase; tyramine oxidase. Cat No: EXWM-1481. | |
| Myreth carboxylic acid | Tertiary oil recovery agent, viscosity reductant. Group: Oil field. Alternative Names: Poly(oxy-1,2-ethanediyl), alpha-carboxymethyl-omega-tetradecyloxy-. CAS No. 38720-61-5. Molecular formula: (C2H4O)nC16H32O3. Catalog: ACM38720615. | |
| Native α-lytic protease | Alpha-lytic protease (aLP) is an alternative specificity protease for proteomics applications. This protease cleaves after T, A, S, and V residues. It geneRates peptides of similar average length as trypsin. aLP was first isolated from the myxobacterium Lysobacter enzymogenes. The pro-form of aLP is 397 amino acids long. In its mature form, aLP is 198 amino acids long. Its tertiary structural core resembles those of pancreatic serine proteases. Group: Enzymes. Synonyms: Alpha-lytic protease; myxobacter α-lytic proteinase; α-lytic proteinase; α-lytic protease; Mycobacterium sorangium α-lytic proteinase; Myxobacter 495 α-lytic proteinase; Alp. α-LP. Storage: -70°C. Form: Supplied as a solution in 10 mM sodium acetate buffer, pH 5.0. Alpha-lytic protease; myxobacter α-lytic proteinase; α-lytic proteinase; α-lytic protease; Mycobacterium sorangium α-lytic proteinase; Myxobacter 495 α-lytic proteinase; Alp. Cat No: NATE-0052. | |
| Native E. coli PreScission Protease | PreScission Protease is a fusion protein of glutathione S-transferase (GST) and human rhinovirus (HRV) type 14 3C protease. The protease specifically recognizes a subset of sequences which include the core amino acid sequence Leu-Phe-Gln/Gly-Pro cleaving between the Gln and Gly residues. Substrate recognition and cleavage are likely to be dependent not only upon primary structural signals, but also upon the secondary and tertiary structures of the fusion protein as well. Applications: During cleavage reactions, it is recommended that samples be removed at various time points and analyzed by sds-page to estimate the yield, purity, and extent of digestion. the amount of prescission protease, temperature and length of incubation required for complete digestion of a given gst fusion partner may vary depending on the fusion partner. optimal conditions for each fusion should be determined in pilot experiments. digestion may be improved by adding triton x-100, tween 20, nonidet, or np40 to a concentration of 0.01%. concentrations of these detergents up to 1% do not inhibit prescission protease. Group: Enzymes. Synonyms: . Purity: >90% by SDS-PAGE. PSP. Activity: >10000 IU/mg. Appearance: Sterile colorless liquid. Storage: Should be stored in small aliquots at -20°C to -80°C for long term. Source: E. coli. PreScission Protease; PSP. Cat No: NATE-0877. | |
| N-Methylquipazine dimaleate | N-Methylquipazine dimaleate, a tertiary amine analog of quipazine, is a 5-HT3 agonist, which has almost the same affinity for 5-HT3 sites as quipazine but unlike the latter, does not bind to 5-HT1B sites. Synonyms: 2-(1-N-Methylpiperazinyl)quinoline dimaleate. CAS No. 171205-17-7. Molecular formula: C14H17N3.(C4H4O4)2. Mole weight: 459.45. | |
| N,N-Dimethyloctadecylamine Oxide | N,N-Dimethyloctadecylamine Oxide is a tertiary amine oxide used as an emulsifying agent. N,N-Dimethyloctadecylamine Oxide is also used to inhibit skin irritation in cosmetics. Group: Biochemicals. Alternative Names: Admox 18; Admox SC 1885; Ammonyx SO; Barlox 18; Barlox 18S; Conco XA 2S; DONO; Dimethylstearylamine Oxide; N,N-Dimethyl-1-octadecanamine Oxide; N,N-Dimethyl-N-octadecylamine Oxide; N,N-Dimethylstearylamine Oxide; N-Stearyldimethylamine N-Oxide; Nissan Unisafe A-SM; Octadecyldimethylamine N-Oxide; Octadecyldimethylamine Oxide; Schercamox DMS; Stearyldimethylamine Oxide; Unisafe A-SM. Grades: Highly Purified. CAS No. 2571-88-2. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Oxyphencyclimine hydrochloride | A new tertiary amine, Oxyphencyclimine hydrochloride, has been investigated for its effects on the peripheral parasympathetic system. Uses: Scientific research. Group: Signaling pathways. CAS No. 125-52-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0954. | |
| Oxytocin Receptor Antagonist, MSC1630296 (OT-R Antagonist, 3- (4- (N- (4-chlorophenyl) -N- (2-oxo-2- (2- (2-oxoindolin-3-ylidene) hydrazinyl) ethyl) sulfamoyl) phenyl) -N- (3- (dimethylamino) propyl) propanamide, Fumarate Salt) | A tertiary sulfonamide-based compound that acts as a high-affinity oxytocin (OT) receptor-selective antagonist (Ki = 650 and 670pM in 125I-OVTA-competitive binding assays using human and rat OT-R, respectively), while displaying 65-, 245-, and 23,000-fold reduced affinity, respectively, toward human vassopressin receptors V1a, V2, and V1b. Shown to effectively inhibit OT- (10nM) induced Ca2+ mobilization in hOT-R-expressing HEK293-EBNA cells (IC50 = 14nM) in vitro and OT-stimulated uterine contractions in rats (1.4 -10mg/kg p.o. or 30mg/kg p.o.) in vivo. Product is supplied as a fumarate salt for enhanced aqueous solubility (20 and 10mg/ml, respectively, in water and HBSS). Group: Biochemicals. Grades: Purified. Pack Sizes: 2mg. Molecular Formula: C??H??ClN?O?S.C?H?O?. US Biological Life Sciences. | Worldwide |
| PEG C11-15 Alkyl ether carboxylic acid | Tertiary oil recovery agent, viscosity reductant. Group: Oil field. Alternative Names: C11-15 Pareth carboxylic acid. CAS No. 68954-90-5. Molecular formula: (C2H4O)nC13H26O3-(C2H4O)nC17H34O3. Catalog: ACM68954905. | |
| PEG C12-13 Alkyl ether carboxylic acid | Tertiary oil recovery agent, viscosity reductant. Group: Oil field. Alternative Names: C12-13 Pareth carboxylic acid. CAS No. 70750-17-3. Molecular formula: (C2H4O)nC14H28O3-(C2H4O)nC15H30O3. Catalog: ACM70750173. | |
| Piperidolate | Piperidolate is a tertiary amine antimuscarinic. It is similar to atropine. It is mainly used in the smooth muscle spasm of the gastrointestinal tract and inhibits intestinal cramp induced by acetylcholine in rats and dogs. Uses: Piperidolate is mainly used in the smooth muscle spasm of the gastrointestinal tract and inhibits intestinal cramp induced by acetylcholine in rats and dogs. Synonyms: 1-Ethyl-3-piperidinyl diphenylacetate;3-Piperidinol, 1-ethyl-, diphenylacetate;Acetic acid, diphenyl-, 1-ethyl-3-piperidyl ester;Alpha-phenyl-benzeneaceticaci1-ethyl-3-piperidinylester;AN 1087;Benzeneacetic acid, alpha-phenyl-, 1-ethyl-3-piperidinyl ester;Dactil;1-Ethylpiperidin-3-yl 2,2-diphenylacetate;N-Ethyl-3-piperidyl diphenylacetate. Grades: >98%. CAS No. 82-98-4. Molecular formula: C21H25NO2. Mole weight: 323.43. | |
| Polyethylene glycol carboxymethyl C11-15-alkyl ether sodium salts | Tertiary oil recovery agent, viscosity reductant. Group: Oil field. Alternative Names: PEG C11-15 Alkyl ether carboxylic acid, sodium salt. CAS No. 68603-23-6. Molecular formula: (C2H4O)nC13H26O3. Na-(C2H4O)nC17H34O3. Na. Catalog: ACM68603236. | |
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