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| Product | Description | |
|---|---|---|
| Antazoline | Antazoline. Group: Biochemicals. Alternative Names: N-(4,5-dihydro-1H-imidazol-2-ylmethyl)-N-(phenylmethyl)aniline. Grades: Highly Purified. CAS No. 91-75-8. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C17H19N3. US Biological Life Sciences. |  Worldwide |
| Antazoline | Antazoline (Phenazoline) is an H1 receptor antagonist that affects the activity of the central nervous system, has a potent antiarrhythmic effect [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Phenazoline. CAS No. 91-75-8. Pack Sizes: 10 mg. Product ID: HY-B1067A. |  |
| Antazoline hemisulfate | Antazoline hemisulfate is the sulfate salt of antazoline, which is a first-generation antihistamine, binding to the histamine H1 receptor and blocking the action of endogenous histamine. Synonyms: Benzyl-(4,5-dihydro-1H-imidazol-2-ylmethyl)-phenyl-amine 0.5 H2SO4; Bis(N-benzyl-4,5-dihydro-N-phenyl-1H-imidazole-2-methylamine) sulphate; Antazoline 0.5 H2SO4; Antastan hemisulfate; Antihistal hemisulfate; Antistine hemisulfate; Histostab hemisulfate; Imidamine hemisulfate; 2-(N-Phenyl-N-benzylaminomethyl)imidazoline sulfate (2:1); 2-(N-Benzylanilinomethyl)-2-imidazoline sulfate (2:1). Grade: ≥90%. CAS No. 84803-70-3. Molecular formula: C17H19N3.(1/2H2SO4). Mole weight: 314.39. |  |
| Antazoline hydrochloride | Antazoline HCl is a first generation antihistamine, binding to the histamine H1 receptor and blocking the action of endogenous histamine. Synonyms: 2-(N-Phenyl-N-benzyl-aminomethyl)imidazoline hydrochloride; Phenazoline hydrochloride; 2-[(N-Benzylanilino)methyl]-2-imidazoline hydrochloride; 4,5-Dihydro-N-phenyl-N-(phenylmethyl)-1H-imidazole-2-methanamine hydrochloride; 2-Phenylbenzylaminomethylimidazoline hydrochloride; 2-Imidazoline, 2-((N-benzylanilino)methyl)-, monohydrochloride. Grade: >98%. CAS No. 2508-72-7. Molecular formula: C17H19N3.HCl. Mole weight: 301.81. | |
| Antazoline hydrochloride | Antazoline (Phenazoline) hydrochloride is a first-generation antihistamine that also has anticholinergic properties and is used to relieve nasal congestion and is also used as eye drops. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Phenazoline hydrochloride. CAS No. 2508-72-7. Pack Sizes: 250 mg; 500 mg; 1 g. Product ID: HY-B1067. | |
| Antazoline Hydrochloride | Antazoline Hydrochloride. Group: Biochemicals. Alternative Names: 4,5-Dihydro-N-phenyl-N-(phenylmethyl)-1H-Imidazole-2-methanamine Hydrochloride 4,5-Dihydro-N-phenyl-N-(phenylmethyl)-1H-Imidazole-2-methanamine Monohydrochloride; 2-[(N-Benzylanilino)methyl]-2-imidazoline Monohydrochloride; 2-(N-Benzylanilinomethyl)-2-imidazoline Hydrochloride; 5512M; Antastan; Antasten; Antazoline chloride; Antazoline hydrochloride; Antihistal; Antistin; Antistina; Antistine hydrochloride; Azalone; Ben-a-hist; Dibistin; Fenazolina; Histazine; Histostab; Imidamine; Phenazoline Hydrochloride. Grades: Highly Purified. CAS No. 2508-72-7. Pack Sizes: 1g. Molecular Formula: C17H20ClN3, Molecular Weight: 301.81. US Biological Life Sciences. | Worldwide |
| Antazoline methanesulfonate | Antazoline methanesulfonate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-((n-benzylanilino)methyl)-2-imidazolinmonomethanesulfonate;2-n-benzylanilinomethylimidazoline;4,5-dihydro-n-phenyl-n-(phenylmethyl)-1h-imidazole-2-methanaminemonomethanes;4,5-dihydro-n-phenyl-n-(phenylmethyl)-1h-imidazole-2-methanaminmonomethane;analergin;antazolinemesylate;antazolinemethanesulfonate;antazolinemethanesulphonate. Product Category: Heterocyclic Organic Compound. CAS No. 3131-32-6. Molecular formula: C18H20N3O3S-. Mole weight: 358.4347. Product ID: ACM3131326. Alfa Chemistry ISO 9001:2015 Certified. Categories: Antazoline mesylate. |  |
| Antazoline methansulfonate | Antazoline methansulfonate is the salt of antazoline, which is a first-generation antihistamine, binding to the histamine H1 receptor and blocking the action of endogenous histamine. Synonyms: Antazoline mesylate; 1H-Imidazole-2-methanamine, 4,5-dihydro-N-phenyl-N-(phenylmethyl)-, methanesulfonate (1:1); Phenazoline methanesulfonate; Antasten mesylate; Histostab mesylate; Imidamine mesylate; 2-(N-Phenyl-N-benzylaminomethyl)imidazoline mesylate; 2-(N-Benzylanilinomethyl)-2-imidazoline mesylate; 4,5-Dihydro-N-phenyl-N-phenylmethyl-1H-imidazole-2-methanamine mesylate. Grade: ≥90%. CAS No. 3131-32-6. Molecular formula: C18H23N3O3S. Mole weight: 361.46. | |
| Antazoline phosphate | Antazoline phosphate is the phosphate salt of antazoline, which is a first-generation antihistamine, binding to the histamine H1 receptor and blocking the action of endogenous histamine. Synonyms: Antazoline HPO. Grade: 95%. CAS No. 154-68-7. Molecular formula: C17H19N3.H3PO4. Mole weight: 363.35. | |
| Antazoline Phosphate | Antazoline Phosphate acts as a histamine H1 receptor blocker, functioning as an antihistamine pharmaceutical. Group: Biochemicals. Alternative Names: Antistine Phosphate; 2-[(N-Benzylanilino)methyl]-2-imidazoline Phosphate; 4,5-Dihydro-N-phenyl-N-(phenylmethyl)-1H-imidazole-2-methanamine Phosphate. Grades: Highly Purified. CAS No. 154-68-7. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Antazoline Phosphate | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsapi standardspharmaceutical toxicology. Alternative Names: 2-[(N-Benzylanilino)methyl]-2-imidazoline dihydrogen phosphate, 2-[(N-Benzylanilino)methyl]-2-imidazoline phosphate (1:1), Antazoline phosphate,Antazoline Phosphate, Antistine phosphate, 4,5-Dihydro-N-phenyl-N-(phenylmethyl)-1H-imidazole-2-methanamine phosphate (1:1). |  |
| Antazoline Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Antazoline sulfate | Antazoline sulfate is the sulfate salt of antazoline, which is a first-generation antihistamine, binding to the histamine H1 receptor and blocking the action of endogenous histamine. Synonyms: 1H-Imidazole-2-methanamine, 4,5-dihydro-N-phenyl-N-(phenylmethyl)-, sulfate (1:1); Phenazoline sulfate; Antasten sulfate; Histostab sulfate; Imidamine sulfate; 2-(N-Phenyl-N-benzylaminomethyl)imidazoline sulfate; 2-(N-Benzylanilinomethyl)-2-imidazoline sulfate; 4,5-Dihydro-N-phenyl-N-phenylmethyl-1H-imidazole-2-methanamine sulfate; 2-Phenyl-benzyl-amino-methylimidazolin sulfate. Grade: 95%. CAS No. 24359-81-7. Molecular formula: C17H19N3.H2O4S. Mole weight: 363.43. | |
| Antazoline sulfate | Antazoline sulfate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Antazoline Sulfate. Product Category: Heterocyclic Organic Compound. CAS No. 24359-81-7. Molecular formula: C17H19N3.H2O4S. Mole weight: 363.436. Product ID: ACM24359817. Alfa Chemistry ISO 9001:2015 Certified. | |
| Antennapedia Leader Peptide (CT) | Antennapedia Leader Peptide (CT), a cell-permeable carrier peptide, is used to deliver the functional domain of certain proteins from the outside to the inside of intact cells. Synonyms: H-Lys-Lys-Trp-Lys-Met-Arg-Arg-Asn-Gln-Phe-Trp-Val-Lys-Val-Gln-Arg-Gly-OH; L-lysyl-L-lysyl-L-tryptophyl-L-lysyl-L-methionyl-L-arginyl-L-arginyl-L-asparaginyl-L-glutaminyl-L-phenylalanyl-L-tryptophyl-L-valyl-L-lysyl-L-valyl-L-glutaminyl-L-arginylglycine. Grade: >95%. Molecular formula: C104H167N35O21S. Mole weight: 2275.76. | |
| Antennapedia Peptide | Antennapedia Peptide, a cell-penetrating 16 amino acid peptide originally derived from the 60 amino acid long homeodomain of the Drosophila transcription factor Antennapedia, is a member of the family of Cell-penetrating peptides. Synonyms: L-Arginyl-L-glutaminyl-L-isoleucyl-L-lysyl-L-isoleucyl-L-tryptophyl-L-phenylalanyl-L-glutaminyl-L-asparaginyl-L-arginyl-L-arginyl-L-methionyl-L-lysyl-L-tryptophyl-L-lysyl-L-lysine; N5-(diaminomethylidene)-L-ornithyl-L-glutaminyl-L-isoleucyl-L-lysyl-L-isoleucyl-L-tryptophyl-L-phenylalanyl-L-glutaminyl-L-asparaginyl-N5-(diaminomethylidene)-L-ornithyl-N5-(diaminomethylidene)-L-ornithyl-L-methionyl-L-lysyl-L-tryptophyl-L-lysyl-L-lysine; Penetratin; Penetratin-1; Arg-Gln-Ile-Lys-Ile-Trp-Phe-Gln-Asn-Arg-Arg-Met-Lys-Trp-Lys-Lys. Grade: ≥98%. CAS No. 188842-14-0. Molecular formula: C104H168N34O20S. Mole weight: 2246.73. | |
| Antennapedia Peptide (43-58), acid | Antennapedia Peptide (43-58), acid, a cell-penetrating peptide corresponding to the region within the DNA binding domain of the Drosophila Antennapedia, is mapped to be responsible for cellular internalization. It is also known as penetratin and has been shown to be able to translocate through the plasma membrane to the cytosol and nucleus of living cells, both at 37°C and 4°C. Synonyms: H-Arg-Gln-Ile-Lys-Ile-Trp-Phe-Gln-Asn-Arg-Arg-Met-Lys-Trp-Lys-Lys-OH; L-arginyl-L-glutaminyl-L-isoleucyl-L-lysyl-L-isoleucyl-L-tryptophyl-L-phenylalanyl-L-glutaminyl-L-asparaginyl-L-arginyl-L-arginyl-L-methionyl-L-lysyl-L-tryptophyl-L-lysyl-L-lysine. Grade: >95%. Molecular formula: C104H168N34O20S. Mole weight: 2246.76. | |
| Antennapedia Peptide (43-58), amide | Antennapedia Peptide (43-58), amide, a cell-penetrating peptide corresponding to the region within the DNA binding domain of the Drosophila Antennapedia, is mapped to be responsible for cellular internalization. It is also known as penetratin and has been shown to be able to translocate through the plasma membrane to the cytosol and nucleus of living cells, both at 37°C and 4°C. Synonyms: H-Arg-Gln-Ile-Lys-Ile-Trp-Phe-Gln-Asn-Arg-Arg-Met-Lys-Trp-Lys-Lys-NH2. Grade: >95%. Molecular formula: C104H169N35O19S. Mole weight: 2245.78. | |
| Antennapedia Peptide (43-58), FAM-labeled | Antennapedia Peptide (43-58), FAM-labeled is an antennapedia peptide (Penetratin) labeled with FAM. It is a 16 amino acid peptide corresponding to the region within the Drosophila Antennapedia DNA binding domain that is mapped to be responsible for cellular internalization. It has been shown to be able to translocate through the plasma membrane to the cytosol and nucleus of living cells, both at 37°C and 4°C. Synonyms: 5-FAM-Arg-Gln-Ile-Lys-Ile-Trp-Phe-Gln-Asn-Arg-Arg-Met-Lys-Trp-Lys-Lys-NH2. Grade: >95%. Molecular formula: C125H179N35O25S. Mole weight: 2604.08. | |
| Antennapedia Peptide, acid | Antennapedia Peptide is a 16 amino-acid residue peptide derived from the homology domain of the 60 amino acid sequence of the Drosophila transcription factor Antennapedia. Antennapedia Peptide has cell penetrating properties that can be conjugated to nucleic acids and other macromolecules. Synonyms: H-Arg-Gln-Ile-Lys-Ile-Trp-Phe-Gln-Asn-Arg-Arg-Met-Lys-Trp-Lys-Lys-OH; Arg-Gln-Ile-Lys-Ile-Trp-Phe-Gln-Asn-Arg-Arg-Met-Lys-Trp-Lys-Lys. Molecular formula: C104H168N34O20S. Mole weight: 2246.85. | |
| Antennapedia Peptide TFA | Antennapedia Peptide, a cell-penetrating 16 amino acid peptide originally derived from the 60 amino acid long homeodomain of the Drosophila transcription factor Antennapedia, is a member of the family of Cell-penetrating peptides. Synonyms: L-arginyl-L-glutaminyl-L-isoleucyl-L-lysyl-L-isoleucyl-L-tryptophyl-L-phenylalanyl-L-glutaminyl-L-asparagyl-L-arginyl-D-arginyl-L-methionyl-L-lysyl-L-tryptophyl-L-lysyl-L-lysine trifluoroacetic acid. Grade: 98%. Molecular formula: C106H169F3N34O22S. Mole weight: 2360.82. | |
| Antennapedia Peptide (TFA) | Antennapedia Peptide TFA, a cell-penetrating 16 amino acid peptide originally derived from the 60 amino acid long homeodomain of the Drosophila transcription factor Antennapedia, is a member of the family of Cell-penetrating peptide. Synonyms: L-Arginyl-L-glutaminyl-L-isoleucyl-L-lysyl-L-isoleucyl-L-tryptophyl-L-phenylalanyl-L-glutaminyl-L-asparaginyl-L-arginyl-L-arginyl-L-methionyl-L-lysyl-L-tryptophyl-L-lysyl-L-lysine trifluoroacetic acid; N5-(diaminomethylidene)-L-ornithyl-L-glutaminyl-L-isoleucyl-L-lysyl-L-isoleucyl-L-tryptophyl-L-phenylalanyl-L-glutaminyl-L-asparaginyl-N5-(diaminomethylidene)-L-ornithyl-N5-(diaminomethylidene)-L-ornithyl-L-methionyl-L-lysyl-L-tryptophyl-L-lysyl-L-lysine trifluoroacetic acid; Penetratin trifluoroacetic acid; Penetratin-1 trifluoroacetic acid; Arg-Gln-Ile-Lys-Ile-Trp-Phe-Gln-Asn-Arg-Arg-Met-Lys-Trp-Lys-Lys.TFA. Grade: ≥98%. Molecular formula: C104H168N34O20S.C2HF3O2. Mole weight: 2360.82. | |
| Anterior Lobe Pituitary Powder(Porcine) | Anterior Lobe Pituitary Powder(Porcine). Categories: betamethasone sodium phosphate; 151-73-5. |  CA, FL & NJ |
| Ant-GTP | Ant-GTP is a crucial recompound for studying GTP-binding protein playing a significant role in elucidating the functions of GTPases such as cell signaling, protein research and development and vesicle transport. By providing a stable source of GTP, ant-GTP facilitates the investigation of various diseases associated with GTPase dysregulation, including cancer, neurodegenerative disorders and cardiovascular diseases. Synonyms: 2'/3'-O-Anthraniloyl-guanosine-5'-triphosphate, Triethylammonium salt. Grade: ≥ 95% by HPLC. Molecular formula: C17H21N6O15P3 (free acid). Mole weight: 642.30 (free acid). | |
| Anthamber | Anthamber (ISO E Super). CAS No. 54464-57-2. Kosher: Y. VIGON Item # 503503. Categories: Speciality Ingredients Suppliers, Fragrances, Perfumers, 1-(2,3,8,8-TETRAMETHYL-1,3,4,5,6,7-HEXAHYDRONAPHTHALEN-2-YL) ETHANONE |  America & Internationally |
| Anthanthrene | Anthanthrene. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Dibenzo[def,mno]chrysene. Product Category: Reference/Calibration Standards. CAS No. 191-26-4. Molecular formula: C22H12. Mole weight: 276.3. Product ID: ACM191264. Alfa Chemistry ISO 9001:2015 Certified. | |
| Anthanthrene | certified Reference Material. Group: Polycyclic aromatic hydrocarbon (pah) standardspolycyclic aromatic hydrocarbons (pahs)environmental food contaminants. Alternative Names: Dibenzo[cd,jk]pyrene,Dibenzo[def,mno]chrysene, Anthanthren, Anthanthrene. | |
| Anthelvencin A | It is produced by the strain of Streptomyces venezuelae. It has the activity of resisting gram positive bacterium, negative bacterium, mycobacterium, yeast and ringworm, has the inhibition to vaccinia virus, dysentery amoeba, and has the effect of repelling nematode in mice. Synonyms: (4S)-(+)-Anthelvencin A; NSC624528; (S)-Anthelvencin A; LS-20251; {4-[((5S)-2-amino(1-pyrrolin-5-yl))carbonylamino]pyrrol-2-yl}-N-{5-[N-(2-amidinoethyl)carbamoyl]-1-methylpyrrol-3-yl}carboxamide. CAS No. 58616-25-4. Molecular formula: C19H25N9O3. Mole weight: 427.46. | |
| Anthelvencin B | It is produced by the strain of Streptomyces venezuelae. It has the activity of resisting gram positive bacterium, negative bacterium, mycobacterium, yeast and ringworm, has the inhibition to vaccinia virus, dysentery amoeba, and has the effect of repelling nematode in mice. Synonyms: Anthelvencine B; DTXSID30911498; N-[5-({5-[(3-Amino-3-iminopropyl)carbamoyl]-1-methyl-1H-pyrrol-3-yl}carbamoyl)-1-methyl-1H-pyrrol-3-yl]-5-iminopyrrolidine-2-carboximidic acid. CAS No. 11011-26-0. Molecular formula: C20H27N9O3. Mole weight: 441.49. | |
| Anther | Anther (Phenyl Ethyl Isoamyl Ether). CAS No. 56011-02-0. FEMA No. 4635. VIGON Item # 503201. Categories: Speciality Ingredients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| Antheraxanthin | Antheraxanthin. Group: Biochemicals. Alternative Names: (3S,5R,6S,3'R)-5,6-Epoxy-5,6-dihydro-b,b-carotene-3,3'-diol; all-trans-Antheraxanthin. Grades: Highly Purified. CAS No. 640-03-9. Pack Sizes: 250ug, 500ug, 1mg. Molecular Formula: C40H56O3, Molecular Weight: 584.87. US Biological Life Sciences. | Worldwide |
| anthocyanidin 3-O-coumaroylrutinoside 5-O-glucosyltransferase | Isolated from the plant Petunia hybrida. It does not act on an anthocyanidin 3-O-rutinoside. Group: Enzymes. Enzyme Commission Number: EC 2.4.1.296. 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-2530; anthocyanidin 3-O-coumaroylrutinoside 5-O-glucosyltransferase; EC 2.4.1.296. Cat No: EXWM-2530. |  |
| anthocyanidin 3-O-glucoside 2''-O-glucosyltransferase | Isolated from Ipomoea nil (Japanese morning glory). Group: Enzymes. Synonyms: 3GGT. Enzyme Commission Number: EC 2.4.1.297. 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-2531; anthocyanidin 3-O-glucoside 2''-O-glucosyltransferase; EC 2.4.1.297; 3GGT. Cat No: EXWM-2531. | |
| anthocyanidin 3-O-glucoside 2'''-O-xylosyltransferase | Isolated from the plants Matthiola incana (stock) and Arabidopsis thaliana (mouse-eared cress). The enzyme has similar activity with the 3-glucosides of pelargonidin, cyanidin, delphinidin, quercetin and kaempferol as well as with cyanidin 3-O-rhamnosyl-(1?6)-glucoside and cyanidin 3-O-(6-acylglucoside). There is no activity with other UDP-sugars or with cyanidin 3,5-diglucoside. Group: Enzymes. Synonyms: uridine 5'-diphosphate-xylose:anthocyanidin 3-O-glucose-xylosyltransferase; UGT79B1. Enzyme Commission Number: EC 2.4.2.51. 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-2681; anthocyanidin 3-O-glucoside 2'''-O-xylosyltransferase; EC 2.4.2.51; uridine 5'-diphosphate-xylose:anthocyanidin 3-O-glucose-xylosyltransferase; UGT79B1. Cat No: EXWM-2681. | |
| anthocyanidin 3-O-glucoside 5-O-glucosyltransferase | Isolated from the plants Perilla frutescens var. crispa, Verbena hybrida, Dahlia variabilis and Gentiana triflora (clustered gentian). It will also act on anthocyanidin 3-O-(6-O-malonylglucoside) and is much less active with hydroxycinnamoylglucose derivatives. There is no activity in the absence of the 3-O-glucoside group. Group: Enzymes. Synonyms: UDP-glucose:anthocyanin 5-O-glucosyltransferase. Enzyme Commission Number: EC 2.4.1.298. 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-2532; anthocyanidin 3-O-glucoside 5-O-glucosyltransferase; EC 2.4.1.298; UDP-glucose:anthocyanin 5-O-glucosyltransferase. Cat No: EXWM-2532. | |
| anthocyanidin 3-O-glucoside 6''-O-acyltransferase | Isolated from the plants Perilla frutescens and Gentiana triflora (clustered gentian). Acts on a range of anthocyanidin 3-O-glucosides, 3,5-di-O-glucosides and cyanidin 3-rutinoside. It did not act on delphinidin 3,3',7-tri-O-glucoside. Recombinant Perilla frutescens enzyme could utilize caffeoyl-CoA but not malonyl-CoA as alternative acyl donor. Group: Enzymes. Enzyme Commission Number: EC 2.3.1.215. 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-2161; anthocyanidin 3-O-glucoside 6''-O-acyltransferase; EC 2.3.1.215. Cat No: EXWM-2161. | |
| anthocyanidin 3-O-glucosyltransferase | The anthocyanidin compounds cyanidin, delphinidin, peonidin and to a lesser extent pelargonidin can act as substrates. The enzyme does not catalyse glucosylation of the 5-position of cyanidin and does not act on flavanols such as quercetin and kaempferol (cf. EC 2.4.1.91 flavonol 3-O-glucosyltransferase). In conjunction with EC 1.14.11.19, leucocyanidin oxygenase, it is involved in the conversion of leucoanthocyanidin into anthocyanidin 3-glucoside. It may act on the pseudobase precursor of the anthocyanidin rather than on the anthocyanidin itself. Group: Enzymes. Synonyms: uridine diphosphoglucose-anthocyanidin 3-O-glucosyltransferase; UDP-glucose:anthocyanidin/flavonol 3-O-glucosyltransferase; UDP-glucose:cyanidin-3-O-glucosyltransferase; UDP-glucose:anthocyanidin 3-O-D-glucosyltransferase; 3-GT. Enzyme Commission Number: EC 2.4.1.115. CAS No. 65607-32-1. 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-2341; anthocyanidin 3-O-glucosyltransferase; EC 2.4.1.115; 65607-32-1; uridine diphosphoglucose-anthocyanidin 3-O-glucosyltransferase; UDP-glucose:anthocyanidin/flavonol 3-O-glucosyltransferase; UDP-glucose:cyanidin-3-O-glucosyltransferase; UDP-glucose:anthocyanidin 3-O-D-glucosyltransferase; 3-GT. Cat No: EXWM-2341. | |
| anthocyanidin reductase [(2R,3R)-flavan-3-ol-forming] | The enzyme participates in the flavonoid biosynthesis pathway found in plants. It catalyses the double reduction of anthocyanidins, producing (2R,3R)-flavan-3-ol monomers required for the formation of proanthocyanidins. While the enzyme from the legume Medicago truncatula (MtANR) can use both NADPH and NADH as reductant, that from the crucifer Arabidopsis thaliana (AtANR) uses only NADPH. Also, while the substrate preference of MtANR is cyanidin>pelargonidin>delphinidin, the reverse preference is found with AtANR. cf. EC 1.3.1.112, anthocyanidin reductase [(2S)-flavan-3-ol-forming]. Group: Enzymes. Synonyms: ANR (gene name) (ambiguous); flavan-3-ol:NAD(P)+ oxidoreductase; anthocyanidin reductase (ambiguous). Enzyme Commission Number: EC 1.3.1.77. CAS No. 93389-48-1. 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-1346; anthocyanidin reductase [(2R,3R)-flavan-3-ol-forming]; EC 1.3.1.77; 93389-48-1; ANR (gene name) (ambiguous); flavan-3-ol:NAD(P)+ oxidoreductase; anthocyanidin reductase (ambiguous). Cat No: EXWM-1346. | |
| anthocyanidin reductase [(2S)-flavan-3-ol-forming] | The enzyme, characterized from Vitis vinifera (grape), participates in the flavonoid biosynthesis pathway. It catalyses the double reduction of anthocyanidins, producing a mixture of (2S,3S)- and (2S,3R)-flavan-3-ols. The enzyme catalyses sequential hydride transfers to C-2 and C-4, respectively. Epimerization at C-3 is achieved by tautomerization that occurs between the two hydride transfers. cf. EC 1.3.1.77, anthocyanidin reductase [(2R,3R)-flavan-3-ol-forming]. Group: Enzymes. Enzyme Commission Number: EC 1.3.1.112. 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-1285; anthocyanidin reductase [(2S)-flavan-3-ol-forming]; EC 1.3.1.112. Cat No: EXWM-1285. | |
| anthocyanin 3-O-sambubioside 5-O-glucosyltransferase | Isolated from the plant Matthiola incana (stock). No activity with anthocyanidin 3-O-glucosides. Group: Enzymes. Enzyme Commission Number: EC 2.4.1.295. 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-2529; anthocyanin 3-O-sambubioside 5-O-glucosyltransferase; EC 2.4.1.295. Cat No: EXWM-2529. | |
| anthocyanin 5-(6'''-hydroxycinnamoyltransferase) | Isolated from the plant Gentiana triflora. Transfers the hydroxycinnamoyl group only to the C-5 glucoside of anthocyanin. Caffeoyl-CoA, but not malonyl-CoA, can substitute as an acyl donor. Group: Enzymes. Enzyme Commission Number: EC 2.3.1.153. CAS No. 198841-53-1. 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-2093; anthocyanin 5-(6'''-hydroxycinnamoyltransferase); EC 2.3.1.153; 198841-53-1. Cat No: EXWM-2093. | |
| anthocyanin 5-O-glucoside 6'''-O-malonyltransferase | Specific for the penultimate step in salvianin biosynthesis. The enzyme also catalyses the malonylation of shisonin to malonylshisonin [cyanidin 3-O-(6''-O-p-coumaryl-β-D-glucoside)-5-(6'''-O-malonyl-β-D-glucoside)]. The compounds 4'''-demalonylsalvianin, salvianin, pelargonidin 3,5-diglucoside and delphinidin 3,5-diglucoside cannot act as substrates. Group: Enzymes. Enzyme Commission Number: EC 2.3.1.172. CAS No. 380229-66-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2113; anthocyanin 5-O-glucoside 6'''-O-malonyltransferase; EC 2.3.1.172; 380229-66-3. Cat No: EXWM-2113. | |
| anthocyanin 6''-O-malonyltransferase | Acts on pelargonidin 3-O-glucoside in dahlia (Dahlia variabilis), delphinidin 3-O-glucoside, and on cyanidin 3-O-glucoside in transgenic petunia (Petunia hybrida). Group: Enzymes. Enzyme Commission Number: EC 2.3.1.171. CAS No. 111070-07-6. 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-2112; anthocyanin 6''-O-malonyltransferase; EC 2.3.1.171; 111070-07-6. Cat No: EXWM-2112. | |
| Anthopleurin-A | Anthopleurin-A is isolated from the sea anemone, Anthopleura xanthogrammica, and has inotropic effects but no chronotropic effects on mammalian heart preparation. Synonyms: H-Gly-Val-Ser-Cys-Leu-Cys-Asp-Ser-Asp-Gly-Pro-Ser-Val-Arg-Gly-Asn-Thr-Leu-Ser-Gly-Thr-Leu-Trp-Leu-Tyr-Pro-Ser-Gly-Cys-Pro-Ser-Gly-Trp-His-Asn-Cys-Lys-Ala-His-Gly-Pro-Thr-Ile-Gly-Trp-Cys-Cys-Lys-Gln-OH (Disulfide bridge: Cys4-Cys46, Cys6-Cys36, Cys29-Cys47); Neurotoxin AX1; AP-A; L-Glutamic acid, glycyl-L-valyl-L-seryl-L-cysteinyl-L-leucyl-L-cysteinyl-L-α-aspartyl-L-seryl-L-α-aspartylglycyl-L-prolyl-L-seryl-L-valyl-L-arginylglycyl-L-asparaginyl-L-threonyl-L-leucyl-L-serylglycyl-L-threonyl-L-leucyl-L-tryptophyl-L-leucyl-L-tyrosyl-L-prolyl-L-serylglycyl-L-cysteinyl-L-prolyl-L-serylglycyl-L-tryptophyl-L-histidyl-L-asparaginyl-L-cysteinyl-L-lysyl-L-alanyl-L-histidylglycyl-L-prolyl-L-threonyl-L-isoleucylglycyl-L-tryptophyl-L-cysteinyl-L-cysteinyl-L-lysyl-, cyclic tris(disulfide); Neurotoxin AX-I; Anthopleurin A (Anthopleura xanthogrammica). Grade: 95%. CAS No. 60880-63-9. Molecular formula: C220H326N64O67S6. Mole weight: 5131.72. | |
| Anthopleurin-A | >88% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Anthra[1,9-cd]pyrazol-6(2H)-one,3-bromo- | Anthra[1,9-cd]pyrazol-6(2H)-one,3-bromo-. Uses: Designed for use in research and industrial production. Additional or Alternative Names: anthra[1,9-cd]pyrazol-6(2H)-one,3-bromo-. Product Category: Heterocyclic Organic Compound. CAS No. 6375-33-3. Molecular formula: C14H7BrN2O. Mole weight: 299.12218. Purity: 0.96. IUPACName: anthra[1,9-cd]pyrazol-6(2H)-one,3-bromo-. Canonical SMILES: C1=CC=C2C(=C1)C3=C4C(=CC=C(C4=NN3)Br)C2=O. Product ID: ACM6375333. Alfa Chemistry ISO 9001:2015 Certified. | |
| Anthracen-9-yl(phenyl)methanone | Anthracen-9-yl(phenyl)methanone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 9-Anthracenyl phenyl ketone; 9-anthraphenone; Methanone,9-anthracenylphenyl; 9-Benzoylanthracene; Ketone,9-anthracenyl phenyl; BIDD:GT0389; Phenyl-anthranyl-keton. Product Category: Heterocyclic Organic Compound. CAS No. 1564-53-0. Molecular formula: C21H14O. Mole weight: 282.335 g/mol. Purity: 0.96. IUPACName: anthracen-9-yl(phenyl)methanone. Canonical SMILES: C1=CC=C(C=C1)C(=O)C2=C3C=CC=CC3=CC4=CC=CC=C42. Density: 1.197g/cm³. Product ID: ACM1564530. Alfa Chemistry ISO 9001:2015 Certified. | |
| Anthracene | Obtained from coal tar. It is an important source of dyestuffs. Group: Biochemicals. Alternative Names: Anthracin; Green Oil; NSC 7958; Paranaphthalene; Tetra Olive N2G. Grades: Highly Purified. CAS No. 120-12-7. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Anthracene | Anthracene is a white to yellow solid with a weak aromatic odor. Sinks in water. (USCG, 1999);DryPowder;WHITE CRYSTALS OR FLAKES.;White to yellow solid with a weak aromatic odor. Group: Carbon nano materials electroluminescence materials organic light-emitting diode (oled) materials sublimed materials. Alternative Names: Paranaphthalene. CAS No. 120-12-7. Product ID: anthracene. Molecular formula: 178.23. Mole weight: C14H10. C1=CC=C2C=C3C=CC=CC3=CC2=C1. InChI=1S / C14H10 / c1-2-6-12-10-14-8-4-3-7-13 (14) 9-11 (12) 5-1 / h1-10H. MWPLVEDNUUSJAV-UHFFFAOYSA-N. |  |
| Anthracene-(1,2,3,4,4a,9a-14c) | Anthracene-(1,2,3,4,4a,9a-14c). Uses: Designed for use in research and industrial production. Additional or Alternative Names: ANTHRACENE-(1,2,3,4,4A,9A-14C). Product Category: Heterocyclic Organic Compound. CAS No. 163702-16-7. Molecular formula: C14H10. Mole weight: 190.34. Purity: 0.96. Product ID: ACM163702167. Alfa Chemistry ISO 9001:2015 Certified. | |
| Anthracene-1,4,9,10-tetraol | 25g Pack Size. Group: Building Blocks, Organics. Formula: C14H10O4. CAS No. 476-60-8. Prepack ID 90026280-25g. Molecular Weight 242.23. See USA prepack pricing. |  |
| Anthracene-2,6-diamine | Anthracene-2,6-diamine. Group: Mof&cof-ligand. Product ID: anthracene-2,6-diamine. Molecular formula: 208.26g/mol. Mole weight: C14H12N2. InChI=1S / C14H12N2 / c15-13-3-1-9-5-12-8-14 (16) 4-2-10 (12) 6-11 (9) 7-13 / h1-8H, 15-16H2. UXOSWMZHKZFJHD-UHFFFAOYSA-N. | |
| Anthracene-2,6-diyl Bis(trifluoromethanesulfonate) | Anthracene-2,6-diyl Bis(trifluoromethanesulfonate). Group: Small molecule semiconductor building blockssemiconductor blocks. CAS No. 594838-61-6. Product ID: [6- (trifluoromethylsulfonyloxy) anthracen-2-yl] trifluoromethanesulfonate. Molecular formula: 474.4g/mol. Mole weight: C16H8F6O6S2. C1=CC (=CC2=CC3=C (C=C21)C=C (C=C3)OS (=O) (=O)C (F) (F)F)OS (=O) (=O)C (F) (F)F. InChI=1S/C16H8F6O6S2/c17-15(18, 19)29(23, 24)27-13-3-1-9-5-12-8-14(28-30(25, 26)16(20, 21)22)4-2-10(12)6-11(9)7-13/h1-8H. ZGOORSQUXBKABZ-UHFFFAOYSA-N. | |
| Anthracene-2-carboxylic acid | Anthracene-2-carboxylic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 613-08-1. Pack Sizes:5g, 1g, 2g. US Biological Life Sciences. | Worldwide |
| Anthracene,9,10-bis(4-methylphenyl)- | Anthracene,9,10-bis(4-methylphenyl)-. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 9,10-Di-p-tolylanthracene, AGN-PC-004FRY, 648973_ALDRICH, AKOS015916499, Anthracene, 9,10-bis(4-methylphenyl)-, I14-51408, 43217-31-8. Product Category: Heterocyclic Organic Compound. CAS No. 43217-31-8. Molecular formula: C28H22. Mole weight: 358.47. Purity: 0.96. IUPACName: 9,10-bis(4-methylphenyl)anthracene. Canonical SMILES: CC1=CC=C(C=C1)C2=C3C=CC=CC3=C(C4=CC=CC=C42)C5=CC=C(C=C5)C. Density: 1.117 g/cm³. Product ID: ACM43217318. Alfa Chemistry ISO 9001:2015 Certified. | |
| Anthracene-9,10-diboronic acid bis(pinacol)ester,95% | Anthracene-9,10-diboronic acid bis(pinacol)ester,95%. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Anthracene-9,10-diboronic acid bis(pinacol) ester, 95%;9,10-Anthracenediboronic acid bis(pinacol) ester;9,10-Bis(4,4,5,5-tetramethyl[1.3.2]dioxaborolan-2-yl)anthracene;9,10-Anthracenediboronic acid bis(pinacol) ester 97%. Product Category: Organic & Printed Electronics. CAS No. 863992-56-7. Molecular formula: C26H36B2O6. Mole weight: 466.18244. Purity: 0.96. IUPACName: 4,4,5,5-tetramethyl-2-[10-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anthracen-9-yl]-1,3,2-dioxaborolane. Canonical SMILES: B1(OC(C(O1)(C)C)(C)C)C2=C3C=CC=CC3=C(C4=CC=CC=C24)B5OC(C(O5)(C)C)(C)C. Density: 1.1±0.1 g/cm³. Product ID: ACM863992567. Alfa Chemistry ISO 9001:2015 Certified. | |
| Anthracene-9,10-dicarboxaldehyde | Anthracene-9,10-dicarboxaldehyde. Group: Small molecule semiconductor building blockssemiconductor blocks. CAS No. 7044-91-9. Product ID: anthracene-9,10-dicarbaldehyde. Molecular formula: 234.25g/mol. Mole weight: C16H10O2. C1=CC=C2C (=C1)C (=C3C=CC=CC3=C2C=O)C=O. InChI=1S / C16H10O2 / c17-9-15-11-5-1-2-6-12 (11) 16 (10-18) 14-8-4-3-7-13 (14) 15 / h1-10H. SBRUFOSORMQHES-UHFFFAOYSA-N. | |
| Anthracene-9,10-dipropionic acid disodium salt | Anthracene-9,10-dipropionic acid disodium salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: ADPA. Product Category: Other Fluorophores. Appearance: Yellow needles. CAS No. 82767-90-6. Molecular formula: C20H162O4. Mole weight: 366.32. Purity: 95%+. Product ID: ACM82767906. Alfa Chemistry ISO 9001:2015 Certified. | |
| ANTHRACENE, 9-BROMO-10-(1-NAPHTHALENYL)- | ANTHRACENE, 9-BROMO-10-(1-NAPHTHALENYL)-. Group: other electronic materials. CAS No. 400607-04-7. Product ID: 9-bromo-10-naphthalen-1-ylanthracene. Molecular formula: 383.3g/mol. Mole weight: C24H15Br. C1=CC=C2C (=C1)C=CC=C2C3=C4C=CC=CC4=C (C5=CC=CC=C53)Br. InChI=1S / C24H15Br / c25-24-21-13-5-3-11-19 (21) 23 (20-12-4-6-14-22 (20) 24) 18-15-7-9-16-8-1-2-10-17 (16) 18 / h1-15H. SYACRXBYRNYMLN-UHFFFAOYSA-N. | |
| Anthracene-9-carboxaldehyde | Anthracene-9-carboxaldehyde. Group: Biochemicals. Alternative Names: 9-Anthraldehyde. Grades: Highly Purified. CAS No. 642-31-9. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C15H10O. US Biological Life Sciences. | Worldwide |
| Anthracene-9-carboxylic acid | Anthracene-9-carboxylic acid (9-Anthracenecarboxylic acid) is an anthracene derivative traditionally used to block and identify Ca 2+ -activated Cl - currents (CaCCs) in various cell types, like diverse smooth muscle cells, epithelial cells and salivary gland cells [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 9-Anthracenecarboxylic acid. CAS No. 723-62-6. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-101329. | |
| Anthracene-9-carboxylic acid-d9 | Anthracene-9-carboxylic acid-d 9 is the deuterium labeled Anthracene-9-carboxylic acid[1]. Anthracene-9-carboxylic acid (9-Anthracenecarboxylic acid) is an anthracene derivative traditionally used to block and identify Ca2+-activated Cl- currents (CaCCs) in various cell types, like diverse smooth muscle cells, epithelial cells and salivary gland cells[2]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: 9-Anthracenecarboxylic acid-d9. CAS No. 1219803-78-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-101329S. | |
| Anthracene,9-fluoro- | Anthracene,9-fluoro-. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 9-FLUOROANTHRACENE. Product Category: Heterocyclic Organic Compound. CAS No. 529-85-1. Molecular formula: C14H9F. Mole weight: 196.2197. Purity: 0.96. IUPACName: 9-fluoroanthracene. Canonical SMILES: C1=CC=C2C(=C1)C=C3C=CC=CC3=C2F. Density: 1.212 g/cm³. Product ID: ACM529851. Alfa Chemistry ISO 9001:2015 Certified. | |
| Anthracene-d10 | Anthracene-d10 is an isotope labelled analogue of Anthracene (A678400), an polycyclic aromatic hydrocarbon found readily as an component in coal tar. Anthracene is also used in the preparation of various dyes. Group: Biochemicals. Grades: Highly Purified. CAS No. 1719-06-8. Pack Sizes: 100mg, 1g. Molecular Formula: C14D10. US Biological Life Sciences. | Worldwide |
| Anthracene oil, acid ext. | Anthracene oil, acid ext. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Anthracene oil, acid ext. Anthracene Oil Extract Residue. Product Category: Heterocyclic Organic Compound. CAS No. 91995-14-1. Purity: 0.96. Product ID: ACM91995141. Alfa Chemistry ISO 9001:2015 Certified. | |
| Anthracene, Practical | Anthracene is a white to yellow solid with a weak aromatic odor. Sinks in water. (USCG, 1999);DryPowder;WHITE CRYSTALS OR FLAKES.;White to yellow solid with a weak aromatic odor. Group: Electroluminescence materials. CAS No. 120-12-7. Product ID: anthracene. Molecular formula: 178.23g/mol. Mole weight: C14H10;(C6H4CH)2;C14H10;C14H10. C1=CC=C2C=C3C=CC=CC3=CC2=C1. InChI=1S / C14H10 / c1-2-6-12-10-14-8-4-3-7-13 (14) 9-11 (12) 5-1 / h1-10H. MWPLVEDNUUSJAV-UHFFFAOYSA-N. | |
| Anthracene, Reagent | Anthracene is a white to yellow solid with a weak aromatic odor. Sinks in water. (USCG, 1999);DryPowder;WHITE CRYSTALS OR FLAKES.;White to yellow solid with a weak aromatic odor. Group: Electroluminescence materials. CAS No. 120-12-7. Product ID: anthracene. Molecular formula: 178.23g/mol. Mole weight: C14H10;(C6H4CH)2;C14H10;C14H10. C1=CC=C2C=C3C=CC=CC3=CC2=C1. InChI=1S / C14H10 / c1-2-6-12-10-14-8-4-3-7-13 (14) 9-11 (12) 5-1 / h1-10H. MWPLVEDNUUSJAV-UHFFFAOYSA-N. | |
| Anthracene Zone Refined (number of passes:30) | Anthracene is a white to yellow solid with a weak aromatic odor. Sinks in water. (USCG, 1999);DryPowder;WHITE CRYSTALS OR FLAKES.;White to yellow solid with a weak aromatic odor. Group: other material building blockscarbon nano materials. CAS No. 120-12-7. Product ID: anthracene. Molecular formula: 178.23g/mol. Mole weight: C14H10;(C6H4CH)2;C14H10;C14H10. C1=CC=C2C=C3C=CC=CC3=CC2=C1. InChI=1S / C14H10 / c1-2-6-12-10-14-8-4-3-7-13 (14) 9-11 (12) 5-1 / h1-10H. MWPLVEDNUUSJAV-UHFFFAOYSA-N. | |
| Anthracene, Zone Refined (number of passes:30) | Anthracene is a white to yellow solid with a weak aromatic odor. Sinks in water. (USCG, 1999);DryPowder;WHITE CRYSTALS OR FLAKES.;White to yellow solid with a weak aromatic odor. Group: Electroluminescence materials. CAS No. 120-12-7. Product ID: anthracene. Molecular formula: 178.23g/mol. Mole weight: C14H10;(C6H4CH)2;C14H10;C14H10. C1=CC=C2C=C3C=CC=CC3=CC2=C1. InChI=1S / C14H10 / c1-2-6-12-10-14-8-4-3-7-13 (14) 9-11 (12) 5-1 / h1-10H. MWPLVEDNUUSJAV-UHFFFAOYSA-N. | |
| Anthracophyllone | Anthracophyllone is an aristolane sesquiterpene isolated from the mushroom Anthracophyllum sp. BCC18695. Synonyms: (-)-Anthracophyllone; 1H-Cyclopropa[a]naphthalene-2,4-dione, 1a,5,6,7,7a,7b-hexahydro-1,1,7,7a-tetramethyl-, (1aS,7S,7aS,7bR)-; (4β,5β,6β,7β)-Aristol-9-ene-1,8-dione. Grade: 96.5%. CAS No. 1801750-22-0. Molecular formula: C15H20O2. Mole weight: 232.32. | |
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