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| Product | Description | |
|---|---|---|
| Nucleating Agent ZC-3 | DryPowder. Group: Polymers. CAS No. 135861-56-2. Product ID: (1R)-1-[(4R,4aR,8aS)-2,6-bis(3,4-dimethylphenyl)-4,4a,8,8a-tetrahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-yl]ethane-1,2-diol. Molecular formula: 414.5g/mol. Mole weight: C24H30O6. CC1=C (C=C (C=C1)C2OCC3C (O2)C (OC (O3)C4=CC (=C (C=C4)C)C)C (CO)O)C. InChI=1S/C24H30O6/c1-13-5-7-17 (9-15 (13)3)23-27-12-20-22 (30-23)21 (19 (26)11-25)29-24 (28-20)18-8-6-14 (2)16 (4)10-18/h5-10, 19-26H, 11-12H2, 1-4H3/t19-, 20+, 21-, 22-, 23?, 24?/m1/s1. YWEWWNPYDDHZDI-JJKKTNRVSA-N. |  |
| Chromoxane | Chromoxane is a surfactant and chemical agent in cosmetology, used for hair activation, bleaching, coloring, and conditioning. Chromoxane is also used as a nucleating agent. Group: Biochemicals. Grades: Highly Purified. CAS No. 70755-50-9. Pack Sizes: 10mg, 50mg. Molecular Formula: C7F15KO5S, Molecular Weight: 520.21. US Biological Life Sciences. |  Worldwide |
| Dehydroabietic Acid 2-Aminoethanol Salt | Dehydroabietic Acid 2-Aminoethanol Salt is the salt form of Dehydroabietic Acid (D229085), a resin acid found commonly in rosin. Dehydroabietic Acid is used in rosin-type nucleating agent for polypropylene (PP). Dehydroabietic Acid is used commonly in the synthesis of surfactants, antioxidants and chiral catalysts. Group: Biochemicals. Alternative Names: (1R,4aS,10aR)-1,2,3,4,4a,9,10,10a-Octahydro-1,4a-dimethyl-7-(1-methylethyl)-1-phenanthrenecarboxylic Acid 2-Aminoethanol. Grades: Highly Purified. CAS No. 642989-65-9. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| Sodium Benzoate | Pharmacopeia & Metrological Institutes Standards; API Standards; Pharmaceutical Toxicology. Uses: For analytical and research use. Group: Reagents. Alternative Names: Benzoate of soda,Sodium Benzoate, Fuminaru, E 221 (nucleating agent), Purox S, Benzoic acid sodium salt (1:1), Antimol, Benzoic acid sodium salt, Sodium benzoate, E 211, Sobenate, SKF-30573Z, E 221. CAS No. 532-32-1. Pack Sizes: 1G. IUPAC Name: sodium;benzoate. |  |
| Sodium Benzoate | Sodium Benzoate. Group: Biochemicals. Alternative Names: Antimol; Benzoate of Soda; E 211; E 221; E 221 (nucleating agent); Fuminaru; Purox S; Sobenate. Grades: Highly Purified. CAS No. 532-32-1. Pack Sizes: 10g. Molecular Formula: C7H5NaO2, Molecular Weight: 144.11. US Biological Life Sciences. | Worldwide |
| Sodium pyrophosphate decahydrate | Sodium pyrophosphate decahydrate can be as a buffering agent, a chelator and a hydrated salt nucleating agent. Sodium pyrophosphate decahydrate can also be used to a raw material for synthetic laundry scent additives [1] [2]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 13472-36-1. Pack Sizes: 100 g. Product ID: HY-W094510. |  |
| (±)-2-Phenylpropanoic Acid | Used in the preparation of ibuprofen derivatives for their anti-inflammatory activity. Also used in nucleation inhibitors in Dutch resolution of diastereomers. Group: Biochemicals. Alternative Names: α-methylbenzeneacetic Acid; Hydratropic acid; (RS)-2-Phenylpropanoic Acid; (RS)-2-Phenylpropionic Acid; (±)-2-Phenylpropanoic Acid; (±)-2-Phenylpropionic Acid; (±)-Hydratropic Acid; (±)-α-Methylphenylacetic Acid; 2-Phenylpropanoic Acid; 2-Phenylpropionic Acid; DL-2-Phenylpropionic Acid; NSC 245033; NSC 42872; dl-PPA; α-Methylbenzeneacetic Acid; α-Methylphenylacetic Acid; α-Phenylpropanoic Acid; α-Phenylpropionic Acid. Grades: Highly Purified. CAS No. 492-37-5. Pack Sizes: 25g. US Biological Life Sciences. | Worldwide |
| 3-keto-5-aminohexanoate cleavage enzyme | Requires Zn2+. The enzyme, isolated from the bacteria Fusobacterium nucleatum and Cloacimonas acidaminovorans, is involved in the anaerobic fermentation of lysine. Group: Enzymes. Synonyms: kce (gene name). Enzyme Commission Number: EC 2.3.1.247. 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-2196; 3-keto-5-aminohexanoate cleavage enzyme; EC 2.3.1.247; kce (gene name). Cat No: EXWM-2196. |  |
| Aspergillus nuclease S1 | Aspergillus nuclease S1 is an endonuclease enzyme derived from Aspergillus oryzae that splits single-stranded DNA (ssDNA) and RNA into oligo- or mononucleotides. Group: Enzymes. Synonyms: endonuclease S1 (Aspergillus); single-stranded-nucleate endonuclease; deoxyribonuclease S1; deoxyribonuclease S1; nuclease S1; Neurospora crassa single-strand specific endonuclease; S1 nuclease; single-strand endodeoxyribonuclease; single-stranded DNA specific endonuclease; single-strand-specific endodeoxyribonuclease; single strand-specific DNase; Aspergillus oryzae S1 nuclease. Enzyme Commission Number: EC 3.1.30.1. CAS No. 37288-25-8. Nuclease. 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-3707; Aspergillus nuclease S1; EC 3.1.30.1; 37288-25-8; endonuclease S1 (Aspergillus); single-stranded-nucleate endonuclease; deoxyribonuclease S1; deoxyribonuclease S1; nuclease S1; Neurospora crassa single-strand specific endonuclease; S1 nuclease; single-strand endodeoxyribonuclease; single-stranded DNA specific endonuclease; single-strand-specific endodeoxyribonuclease; single strand-specific DNase; Aspergillus oryzae S1 nuclease. Cat No: EXWM-3707. | |
| Benproperine phosphate | Benproperine phosphate is an orally active, potent actin-related protein 2/3 complex subunit 2 (ARPC2) inhibitor. Benproperine phosphate attenuates the actin polymerization rate of action polymerization nucleation by impairing Arp2/3 function. Benproperine phosphate has the potential for a cough suppressant and suppresses cancer cell migration and tumor metastasis [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 19428-14-9. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-114657A. | |
| Benproperine phosphate | Benproperine phosphate is an orally active, potent actin-related protein 2/3 complex subunit 2 (ARPC2) inhibitor. Benproperine phosphate attenuates the actin polymerization rate of action polymerization nucleation by impairing Arp2/3 function. Benproperine phosphate has the potential for a cough suppressant and suppresses cancer cell migration and tumor metastasis. Group: Inhibitors. Alternative Names: 1-[2-(2-benzylphenoxy)-1-methylethyl]piperidine phosphate;BENPROPERINE PHOSPHATE;BENPROPERINE PHOSPHATE CP2000;1-(2-Benzylphenoxy)-2-piperidinopropane phosphate;1-[2-(2-Benzylphenoxy)-1-methylethyl]piperidine monophosphate;ASA 158-5;Blascorid;Piperidine. CAS No. 19428-14-9. Molecular formula: C21H27NO?H3O4P. Mole weight: 407.45. Appearance: Solid. Purity: 0.9923. Canonical SMILES: CC (N1CCCCC1)COC2=CC=CC=C2CC3=CC=CC=C3. O=P (O) (O)O. Catalog: ACM19428149. |  |
| Collagenase/Neutral Protease Blend (GMP Grade) | NATE-1917 is an avian and mammalian tissue-free Collagenase and neutral protease enzyme blend produced under GMP quality conditions. Applications: Nate-1917 is specifically designed for stem cell isolation from human and other adipose tissue with following advantages:o a single, sterile, ready-to-use vial containing both collagenase and neutral protease can digest up to 280g of adipose tissue with best-in-class gmp quality and shelf life of up to 72 months.o currently included in ide applications approved by the u.s. fda for alopecia, chronic heart failure, hamstring injuries, osteoarthritis of the knee, and hand manifestations of scleroderma.o research protocols are a...sociation of nucleated cells from adipose tissue.o produced using avian and mammalian tissue-free raw materials, aseptic processes and sterile filtration under gmp guidelines to assure the lowest levels of impurities and stringent quality standards. Group: Enzymes. Synonyms: Collagenase/Neutral Protease Blend; GMP, Collagenase/Neutral Protease Blend; Collagenase; Neutral Protease; GMP. Collagenase. Stability: 48 months at -15 to -25° C. Appearance: White lyophilizate. Source: Clostridium histolyticum/Bacillus polymyxa. Collagenase/Neutral Protease Blend; GMP, Collagenase/Neutral Protease Blend; Collagenase; Neutral Protease; GMP. Pack: 1 vial, 35 mg. Cat No: NATE-1917. | |
| DL-Leucine | DL-Leucine is a racemic mixture of the D- and L- enantiomers of Leucine. DL-Leucine is used to form benzimidazole and pyrimidine hydroxy azo dyes with various transition metals. DL-Leucine may be used for the evaluation of chiral amino acid separation techniques. DL-Leucine is used for the following applications: Used as a standard for the measurement of free amino acids Used in the process of tritiated leucine uptake Used in solution preparation (various organics were used in different combinations and concentrations to model complex surface tension effects, DL-Leucine is one of them). It is chosen due to its presence in atmospheric aerosols and ice nucleation activity as well as for its surfactant character. Group: Amino acids. Alternative Names: (±)-Amino-4-methylpentanoic acid. CAS No. 328-39-2. Molecular formula: (CH3)2CHCH2CH(NH2)CO2H. Mole weight: 131.17. Canonical SMILES: CC(C)CC(N)C(O)=O. ECNumber: 206-328-2. Catalog: ACM328392-1. | |
| In-situ multilayer NbOx-Nb2C MXene heterojunction | 1) Excellent conductivity to ensure the rapid transfer of charges. 2) Stable structure to promote ion transmission and sulfur loading. 3) Sufficient active sites to achieve anchoring of polysulfides and uniform nucleation of Li2S. 4) Higher tap density improves the volumetric energy density of the battery. Obtaining such a versatile high-density host requires reasonable material selection and design. Uses: Energy storage, catalysis, analytical chemistry, mechanics, adsorption, biology, microelectronics, sensors, etc. Group: Mxenes materials. 0.99. | |
| In-situ multilayer TiOx-Ti3C2 MXene heterojunction | 1) Excellent conductivity to ensure the rapid transfer of charges. 2) Stable structure to promote ion transmission and sulfur loading. 3) Sufficient active sites to achieve anchoring of polysulfides and uniform nucleation of Li2S. 4) Higher tap density improves the volumetric energy density of the battery. Obtaining such a versatile high-density host requires reasonable material selection and design. Uses: Energy storage, catalysis, analytical chemistry, mechanics, adsorption, biology, microelectronics, sensors, etc. Group: Mxenes materials. 0.99. | |
| In-situ multilayer VOx-V2C MXene heterojunction | 1) Excellent conductivity to ensure the rapid transfer of charges. 2) Stable structure to promote ion transmission and sulfur loading. 3) Sufficient active sites to achieve anchoring of polysulfides and uniform nucleation of Li2S. 4) Higher tap density improves the volumetric energy density of the battery. Obtaining such a versatile high-density host requires reasonable material selection and design. Uses: Energy storage, catalysis, analytical chemistry, mechanics, adsorption, biology, microelectronics, sensors, etc. Group: Mxenes materials. 0.99. | |
| Jasplakinolide | Jasplakinolide acts as an actin stabilizing agent that stabilizes actin filaments and promotes actin polymerization. It is also a potent inhibitor of breast and prostrate carcinoma cell proliferation. It potently competes with phalloidin for actin binding and induces actin polymerization by stimulating actin filament nucleation in vitro. It induces polymerization of monomeric actin into amorphous masses and disrupts actin filaments in vivo. It is cell permeable and affects chromosome movement in studies. It has insecticidal, antiproliferative and fungicidal activity. It is useful for investigating cell processes mediated by actin depolymerization and polymerization. Synonyms: NSC 613009; NSC613009; NSC-613009; [2S-[1(S*),2R*,4E,6S*,8R*]]-N-[2-Bromo-N-[N-(8-hydroxy-2,4,6-trimethyl-1-oxo-4-nonenyl)-L-alanyl]-N-methyl-D-tryptophyl]-3-(4-hydroxyphenyl)-β-alanine ρ-Lactone; 1-Oxa-5,8,11-triazacyclononadecane β-alanine deriv.; (+)-Jasplakinolide; Cyclo[(3R)-3-(4-hydroxyphenyl)-β-alanyl-(2S,4E,6R,8S)-8-hydroxy-2,4,6-trimethyl-4-nonenoyl-L-alanyl-2-bromo-N-methyl-D-tryptophyl]. Grades: ≥97% by HPLC. CAS No. 102396-24-7. Molecular formula: C36H45BrN4O6. Mole weight: 709.67. |  |
| Native Aspergillus oryzae Nuclease S1 | Nuclease S1 isolated from Aspergillus oryzae exhibits endo-and exolytic hydrolytic activity for the phosphodiester bonds of single-stranded DNA and RNA yielding 5-phosphomononucleotide and 5-phosphooligonucleotide end-products. It is used to digest non-annealed polynucleotide tails and hairpin loops in RNA and DNA duplexes and can be used to convert superhelical DNA to the linear form. The nuclease s1 enzyme from aspergillus oryzae has the ability to degrade single-stranded oligonucleotides composed of either deoxynucleotides or ribonucleotides. Applications: Nuclease s1 from aspergillus oryzae has been used in a study to assess a bi ochemical method for mapping mutational...e S1 nuclease; EC 3.1.30.1; 37288-25-8. Enzyme Commission Number: EC 3.1.30.1. CAS No. 37288-25-8. Nuclease. Storage: -20°C. Form: Solution containing 30 mM sodium acetate, 50 mM NaCl, 1 mM ZnCl2, 50% glycerol, 2 mg/ml protein. Source: Aspergillus oryzae. endonuclease S1 (Aspergillus); single-stranded-nucleate endonuclease; deoxyribonuclease S1; deoxyribonuclease S1; nuclease S1; Neurospora crassa single-strand specific endonuclease; S1 nuclease; single-strand endodeoxyribonuclease; single-stranded DNA specific endonuclease; single-strand-specific endodeoxyribonuclease; single strand-specific DNase; Aspergillus oryzae S1 nuclease; EC 3.1.30.1; 37288-25-8. Cat No: NATE-0492. | |
| Poly (3, 4-ethylenedioxythiophene)-poly (styrenesulfonate) | 1.1% in H2O, surfactant-free, high-conductivity grade. Uses: Pedot:pss can be used as an electrode material with high mobility for charge carriers. it can be used for a wide range of energy based applications such as organic photovoltaics (opv), perovskite solar cells (dsscs), organic light emitting diodes (oleds) and other biomedical sensors.used to prepare highly transparent conductive coating formulations. primary and secondary nucleation by introducing pedot:pss in a hydrogel was studied.virtually 100% absorption from 900-2,000 nm. no absorption maximum from 400-800 nm. conductive polymer blend. Group: 3d printing materials bioelectronic materials organic light-emitting diode (oled) materials organic solar cell (opv) materials. Alternative Names: Poly(2,3-dihydrothieno-1,4-dioxin)-poly(styrenesulfonate), Orgacon ICP 1050, PEDOT:PSS. Pack Sizes: 100 g. Product ID: 2,3-dihydrothieno[3,4-b][1,4]dioxine; (E)-2-phenylethenesulfonic acid. Molecular formula: 326.4g/mol. Mole weight: C14H14O5S2. C1COC2=CSC=C2O1. C1=CC=C(C=C1)C=CS(=O)(=O)O. InChI=1S/C8H8O3S.C6H6O2S/c9-12(10, 11)7-6-8-4-2-1-3-5-8; 1-2-8-6-4-9-3-5(6)7-1/h1-7H, (H, 9, 10, 11); 3-4H, 1-2H2/b7-6+. BGAWZPQKJPTIEA-UHDJGPCESA-N. 1.3 wt % dispersion in H2O, conductive grade. | |
| Sapienic acid sodium | Sapienic acid sodium is a fatty acid commonly found on the skin and in mucosa. Sapienic acid sodium has variable antimicrobial activities against Gram-positive and Gram-negative bacteria found on the skin and in the oral cavity. Sapienic acid sodium is active against Streptococcus sanguinis , Streptococcus mitis and Fusobacterium nucleatum with MBC values of 31.3 μg/mL, 375.0 μg/mL and 93.8 μg/mL, respectively [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 217477-25-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-130187A. | |
| Serratia marcescens nuclease | Hydrolyses double- or single-stranded substrate. Group: Enzymes. Synonyms: endonuclease (Serratia marcescens); barley nuclease; plant nuclease I; nucleate endonuclease. Enzyme Commission Number: EC 3.1.30.2. CAS No. 9025-65-4. 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-3708; Serratia marcescens nuclease; EC 3.1.30.2; 9025-65-4; endonuclease (Serratia marcescens); barley nuclease; plant nuclease I; nucleate endonuclease. Cat No: EXWM-3708. | |
| SMIFH2 | SMIFH2 is an inhibitor of formin homology 2 (FH2) domains. SMIFH2 prevents formin-mediated actin nucleation and barbed end elongation, disrupts formin-dependent actin cytoskeletal structures in fission yeast and mammalian NIH 3T3 fibroblasts. Synonyms: SMIFH-2; SMIFH 2; SMIFH2; 1-(3-Bromophenyl)-5-(2-furanylmethylene)dihydro-2-thioxo-4,6(1H,5H)-pyrimidinedione; (5E)-1-(3-bromophenyl)-5-(furan-2-ylmethylidene)-2-sulfanylidene-1,3-diazinane-4,6-dione. Grades: ≥99% by HPLC. CAS No. 340316-62-3. Molecular formula: C15H9BrN2O3S. Mole weight: 377.21. | |
| SPL-B | SPL-B is an orally active inhibitor of transforming acidic coiled-coil protein (TACC3) exhibiting an inhibitory effect against the nucleation of centrosome microtubules in ovarian cancer cells, without affecting spindle assembly in normal cells. SPL significantly inhibits mitosis in cancer cells and tumor growth. Uses: Antitumor agent. Synonyms: 8-[[ethyl(pyridin-4-ylmethyl)amino]methyl]-7-hydroxy-4-(2-oxochromen-3-yl)chromen-2-one. Grades: 98%. CAS No. 1465248-60-5. Molecular formula: C27H22N2O5. Mole weight: 454.47. | |
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