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| Product | Description | |
|---|---|---|
| Camobucol | Camobucol (AGIX 4207) is an orally active, phenolic antioxidant and anti-inflammatory compound with antirheumatic properties. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AGIX 4207. CAS No. 216167-92-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 20 mg. Product ID: HY-14916. |  |
| Camonsertib | Camonsertib (RP-3500) is an orally active, selective ATR kinase inhibitor (ATRi) with an IC 50 of 1.00 nM in biochemical assays. Camonsertib shows 30-fold selectivity for ATR over mTOR (IC 50=120 nM) and >2,000-fold selectivity over ATM, DNA-PK, and PI3Kα kinases. Camonsertib has potent antitumor activity [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RP-3500; ATR inhibitor 4. CAS No. 2417489-10-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139609. | |
| Camostat mesylate | Camostat mesylate (Camostat mesilate) is an orally active, synthetic serine protease inhibitor for chronic pancreatitis. Camostat mesylate, an inhibitor of TMPRSS2 , shows antiviral activity against SARS-CoV-2. Camostat mesylate also inhibits the activity of prostasin, trypsin, and matriptase [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Camostat mesilate; FOY305; FOY-S980. CAS No. 59721-29-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-13512. | |
| Camostat Mesylate | Orally active, non-peptide proteolitic enzyme inhibitor with anti-trypsin and anti-plasmin activities, related structurally to gabexate. Protease inhibitor. Camostat mesilate is a serine protease inhibitor that inhibits plasmin, kallikrein, thrombin as well as trypsin, which attenuates pancreatic fibrosis. It reduces weight gain and improves metabolism in obese rodent models. It is in clinical use (in Japan) for pancreatitis. Camostat has been found to inhibit influenza virus replication in human tracheal epithelial cells and is also a direct prostasin inhibitor which may be useful in reducing sodium transport in cystic fibrosis. Additionally it has been shown to reduce infection of Calu-3 lung cells by SARS-CoV-2 (the coronavirus responsible for COVID-19) via inhibition of the serine protease TMPRSS2 required for viral spike protein priming. Group: Biochemicals. Alternative Names: 4- [ [4- [ (Aminoiminomethyl) amino] benzoyl] oxy] benzeneacetic Acid 2-(Dimethylamino)-2-oxoethyl Ester Methanesulfonate; FOY 305; FOY-S 980; Foipan. Grades: Highly Purified. CAS No. 59721-29-8. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C??H??N?O?S. US Biological Life Sciences. |  Worldwide |
| Camostat Mesylate | Camostat (INN) or FOY-305 is a serine protease inhibitor. Serine protease enzymes have a variety of functions in the body, and so camostat has a diverse range of uses. It is used in the treatment of some forms of cancer and is also effective against some viral infections, as well as inhibiting fibrosis in liver or kidney disease orpancreatitis. Uses: Trypsin inhibitors. Synonyms: 4-(2-(2-(dimethylamino)-2-oxoethoxy)-2-oxoethyl)phenyl 4-guanidinobenzoate methanesulfonate; Camostat Mesilate; Camostat Mesylate; FOY 305; FOY-305; FOY305. Grades: >98%. CAS No. 59721-29-8. Molecular formula: C20H22N4O5.CH4O3S. Mole weight: 494.52. |  |
| Camostat Mesylate-D6 | Camostat mesylate-D6 is a labelled analogue of Camostat mesylate (C150300). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C21H20D6N4O8S, Molecular Weight: 500.56. US Biological Life Sciences. | Worldwide |
| Camoteskimab | Camoteskimab (AVTX-007) is an anti-IL-18 monoclonal antibody with fully humanized, high-affinity. Camoteskimab is promising for research of cardiovascular diseases and autoinflammatory diseases, including adult-onset Stills disease (AOSD) and multiple myeloma [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: AVTX-007; CERC-007; MEDI 2338. CAS No. 2492472-82-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99491. | |
| cAMP-AM | cAMP-AM is a membrane-permeant precursor of cAMP, the second messenger. cAMP is released after permeation and metabolism of cAMP-AM by esterases, then it is metabolized to produce a pulse-type signal. Synonyms: Adenosine- 3', 5'- monophosphate, acetoxymethyl ester. Grades: ≥ 97% by HPLC for mixture of isomers. CAS No. 159764-93-9. Molecular formula: C13H16O8N5P. Mole weight: 401.3. | |
| Campathecin Impurity 1 | Campathecin Impurity 1. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (R)-4-ethyl-4-hydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione. Molecular Formula: C20H16N2O4. Mole Weight: 348.35. Catalog: APB04617. |  |
| Campathecin Impurity 10 | Campathecin Impurity 10. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (S)-4-ethyl-4-hydroxy-10-methoxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione. Molecular Formula: C21H18N2O5. Mole Weight: 378.38. Catalog: APB04612. | |
| Campathecin Impurity 11 | Campathecin Impurity 11. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (R)-4-ethyl-4,9-dihydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione. Molecular Formula: C20H16N2O5. Mole Weight: 364.35. Catalog: APB04611. | |
| Campathecin Impurity 12 | Campathecin Impurity 12. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (S)-2-hydroxy-7-(2-hydroxy-1-oxobutan-2-yl)-9-oxo-9,11-dihydroindolizino[1,2-b]quinoline-8-carbaldehyde. Molecular Formula: C20H16N2O5. Mole Weight: 364.35. Catalog: APB04608. | |
| Campathecin Impurity 13 | Campathecin Impurity 13. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (S)-4-ethyl-4-hydroxy-10-nitro-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione. Molecular Formula: C20H15N3O6. Mole Weight: 393.35. Catalog: APB04609. | |
| Campathecin Impurity 14 | Campathecin Impurity 14. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (S)-4-ethyl-4-hydroxy-9-methoxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione. Molecular Formula: C21H18N2O5. Mole Weight: 378.38. Catalog: APB04610. | |
| Campathecin Impurity 15 | Campathecin Impurity 15. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (S)-4-ethyl-9-hydroxy-3,14-dioxo-3,4,12,14-tetrahydro-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-4-yl acetate. Molecular Formula: C22H18N2O6. Mole Weight: 406.39. Catalog: APB04607. | |
| Campathecin Impurity 16 | Campathecin Impurity 16. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (S)-9-amino-4-ethyl-4-hydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione. Molecular Formula: C20H17N3O4. Mole Weight: 363.37. Catalog: APB04606. | |
| Campathecin Impurity 17 | Campathecin Impurity 17. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (S)-4-ethyl-4,10-dihydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione. CAS No. 67656-30-8. Molecular Formula: C20H16N2O5. Mole Weight: 364.35. Catalog: APB67656308. | |
| Campathecin Impurity 18 | Campathecin Impurity 18. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (S)-4,11-diethyl-4-hydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione. Molecular Formula: C22H20N2O4. Mole Weight: 376.41. Catalog: APB04605. | |
| Campathecin Impurity 19 | Campathecin Impurity 19. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (S)-10-amino-4-ethyl-4-hydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione. Molecular Formula: C20H17N3O4. Mole Weight: 363.37. Catalog: APB04604. | |
| Campathecin Impurity 2 | Campathecin Impurity 2. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (R)-4,11-diethyl-4,9-dihydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione. CAS No. 647852-82-2. Molecular Formula: C22H20N2O5. Mole Weight: 392.4. Catalog: APB647852822. | |
| Campathecin Impurity 20 | Campathecin Impurity 20. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (4S)-4,11-diethyl-4,12-dihydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione. Molecular Formula: C22H20N2O5. Mole Weight: 392.4. Catalog: APB04603. | |
| Campathecin Impurity 3 | Campathecin Impurity 3. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (R)-4-hydroxy-4-vinyl-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione. Molecular Formula: C20H14N2O4. Mole Weight: 346.34. Catalog: APB04616. | |
| Campathecin Impurity 5 | Campathecin Impurity 5. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (S)-4-ethyl-4-hydroxy-10-methoxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione. CAS No. 39026-92-1. Molecular Formula: C21H18N2O5. Mole Weight: 378.38. Catalog: APB39026921. | |
| Campathecin Impurity 6 | Campathecin Impurity 6. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (S)-4,11-diethyl-4-hydroxy-10-methoxy-3,14-dioxo-3,4,12,14-tetrahydro-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-9-yl [1,4'-bipiperidine]-1'-carboxylate. Molecular Formula: C34H40N4O7. Mole Weight: 616.7. Catalog: APB04615. | |
| Campathecin Impurity 7 | Campathecin Impurity 7. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 3, 10-diethyl-1, 13-dioxo-1, 3, 11, 13-tetrahydrofuro[3', 4':6, 7]indolizino[1, 2-b]quinolin-8-yl [1,4'-bipiperidine]-1'-carboxylate. Molecular Formula: C32H36N4O5. Mole Weight: 556.65. Catalog: APB04613. | |
| Campathecin Impurity 8 | Campathecin Impurity 8. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (S)-4,11-diethyl-4-hydroxy-3,14-dioxo-3,4,12,14-tetrahydro-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-9-yl 2'-hydroxy-[1,4'-bipiperidine]-1'-carboxylate. CAS No. 1346597-39-4. Molecular Formula: C33H38N4O7. Mole Weight: 602.68. Catalog: APB1346597394. | |
| Campathecin Impurity 9 | Campathecin Impurity 9. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (S)-4,11-diethyl-4-hydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione. Molecular Formula: C22H20N2O4. Mole Weight: 376.41. Catalog: APB04614. | |
| cAMP-Bn | cAMP-Bn is a precursor of cAMP, the second messenger. The polar cAMP is released after cAMP-Bn is hydrolyzed to produce an elevated cAMP level for a prolonged period. Synonyms: Adenosine- 3', 5'- monophosphate, benzyl ester. Grades: ≥ 95% by HPLC for mixture of isomers. CAS No. 62742-71-6. Molecular formula: C17H18N5O6P. Mole weight: 419.3. | |
| cAMP (Cyclic Adenosine Monophosphate, Cyclic AMP, Adenosine 3'5'-cyclic Monophosphate) 99+% (HPLC) | Cyclic adenosine monophosphate (cAMP, cyclic AMP or 3'-5'-cyclic adenosine monophosphate) is a second messenger important in many biological processes. cAMP is derived from adenosine triphosphate (ATP) and used for intracellular signal transduction in many different organisms, conveying the cAMP-dependent pathway. Group: Biochemicals. Alternative Names: Cyclic AMP-3',5'; Adenosine-3':5'-cyclic monophosphoric acid; Adenosine 3',5'-cyclophosphoric acid. Grades: Highly Purified. CAS No. 60-92-4. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| cAMP (Cyclic Adenosine Monophosphate, Cyclic AMP, Adenosine 3'5'-cyclic Monophosphate) (HRP) | Cyclic Adenosine Monophosphate is a hydrophilic secondary messenger that is part of the cellular signal transduction pathway. It is produced by enzymatic methods on the molecule ATP by the enzyme adenylyl cyclase. It interacts with receptor proteins on the surface of a cell membrane following an intracellular signal produced by hormones or neurotransmitters. Cyclic AMP activates Protein Kinase A (PKA) catalytic ability. This activated PKA molecule transfers phosphate from ATP to different amino acid sequences. These phosphorylated amino acids can regulate calcium ion channels allowing calcium to move across the cellular membrane. Group: Biochemicals. Grades: Purified. Pack Sizes: 500ul. US Biological Life Sciences. | Worldwide |
| cAMP-dependent protein kinase | cAMP is required to activate this enzyme. The inactive holoenzyme of cAMP-dependent protein kinase is a tetramer composed of two regulatory (R) and two catalytic (C) subunits. cAMP causes the dissociation of the inactive holoenzyme into a dimer of regulatory subunits bound to four cAMP molecules and two free monomeric catalytic subunits [i.e. R2C2 + 4 cAMP = R2(cAMP)4 + 2 C]. Group: Enzymes. Synonyms: PKA; PKA C; protein kinase A; STK22. Enzyme Commission Number: EC 2.7.11.11. CAS No. 142008-29-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3130; cAMP-dependent protein kinase; EC 2.7.11.11; 142008-29-5; PKA; PKA C; protein kinase A; STK22. Cat No: EXWM-3130. |  |
| cAMP-dependent Protein Kinase catalytic subunit from Murine, Recombinant | The catalytic subunit of cAMP-dependent Protein Kinase (PKA) is a serine/threonine protein kinase, which combines, in the absence of cAMP, with the regulatory subunit to form the inactive PKA holoenzyme. Since this is the free catalytic subunit alone, no cAMP is required for activation. Group: Enzymes. Synonyms: Protein Kinase A catalytic subunit; Protein kinase A; PKA; PKAC; cAMP-dependent protein kinase catalytic subunit; PRKAC. Enzyme Commission Number: EC 2.7.11.11. Mole weight: 38 kDa. Storage: Store at -20° C. Form: 50 mM NaCl, 20 mM Tris-HCl (pH 7.5 at 25°C), 1 mM Na2 EDTA, 2 mM DTT and 50% glycerol. Source: E. coli. Species: Murine. Protein Kinase A catalytic subunit; Protein kinase A; PKA; PKAC; cAMP-dependent protein kinase catalytic subunit; PRKAC. Cat No: NATE-1888. | |
| Camp-dependent protein kinase inhibitor-alpha(5-22)amide(human, mouse, rabbit, rat) | Heterocyclic Organic Compound. Alternative Names: THR-THR-TYR-ALA-ASP-PHE-ILE-ALA-SER-GLY-ARG-THR-GLY-ARG-ARG-ASN-ALA-ILE-NH2;PKA INHIBITOR (5-22) AMIDE;PKI (5-22), AMIDE;PKI-ALPHA (5-22) AMIDE (HUMAN, MOUSE, RABBIT, RAT);PROTEIN KINASE A INHIBITOR (5-22) AMIDE;WIPTIDE;TTYADFIASGRTGRRNAI-NH2;H-THR-THR-T. CAS No. 100853-58-5. Molecular formula: C84H137N29O26. Mole weight: 1969.17. Purity: 0.96. IUPACName: H-THR-THR-TYR-ALA-ASP-PHE-ILE-ALA-SER-GLY-ARG-THR-GLY-ARG-ARG-ASN-ALA-. Canonical SMILES: CCC (C)C (C (=O)N)NC (=O)C (C)NC (=O)C (CC (=O)N)NC (=O)C (CCCNC (=N)N)NC (=O)C (CCCNC (=N)N)NC (=O)CNC (=O)C (C (C)O)NC (=O)C (CCCNC (=N)N)NC (=O)CNC (=O)C (CO)NC (=O)C (C)NC (=O)C (C (C)CC)NC (=O)C (CC1=CC=CC=C1)NC (=O)C (CC (=O)O)NC (=O)C (C)NC (=O)C (CC2=CC=C (C=C2)O)NC (=O)C (C (C)O)NC (=O)C (C (C)O)N. Catalog: ACM100853585. |  |
| Campestanol | Campestanol is a phytosterol that can be found in plant food. Campestanol lowers serum cholesterol and low-density lipoprotein. Campestanol can be used for the research of metabolic disorders [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 474-60-2. Pack Sizes: 500 μg; 1 mg. Product ID: HY-113288. | |
| Campestanol | Campestanol. Group: Biochemicals. Alternative Names: 5a-Cholestan-24(RS)-methyl-3b-ol; (3b,5a,24R)-Ergostan-3-ol; 24b-Ethylcholestanol. Grades: Highly Purified. CAS No. 474-60-2. Pack Sizes: 1mg. Molecular Formula: C28H50O. US Biological Life Sciences. | Worldwide |
| Campesterol | Campesterol. Group: Biochemicals. Grades: Highly Purified. CAS No. 474-62-4. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C28H48O. US Biological Life Sciences. | Worldwide |
| Campesterol | Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects. Uses: Scientific research. Group: Natural products. CAS No. 474-62-4. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-N1459. | |
| Campesterol | Campesterol is a phytosterol, primarily found in nuts, fruits, legumes and seeds. It is poorly absorbed in humans and competitively inhibits the absorption of cholesterol. lt decreases the transcription of genes involved in cholesterol metabolism in hepatocytes and enterocytes and has positive impact in treatment of cardiovascular disease. lt was used as standard in GC1 and HPLC2 analysis of oil samples from plants. Synonyms: Campest-5-en-3beta-ol; Ergost-5-en-3beta-ol, (24R)-; Ergost-5-en-3-ol, (3beta,24R)-; 24α-Methyl-5-cholesten-3β-ol. Grades: >98%. CAS No. 474-62-4. Molecular formula: C28H48O. Mole weight: 400.68. | |
| campesterol-d6 | campesterol-d6. Group: Others. Synonyms: 26,27-hexadeuteriocampest-5-en-3ss-ol. Purity: >99%. Mole weight: 406.717. Stability: 6 Months. Storage: -20°C. Avanti Polar Lipids; lipid products; sterols; sterols products; singnal transduction; cell pathways; campesterol-d6; campesterol-d6; 26,27-hexadeuteriocampest-5-en-3ss-ol. Cat No: STEZ-060. | |
| Campesterol-d7 (Mixture of Diastereomers) | Labeled Campesterol. A phytosterol, which may inhibit the intestinal absorption of cholesterol. Group: Biochemicals. Alternative Names: 5-Cholesten-24(RS)-methyl-d3-3 β-ol-d7. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Camphene | Camphene. CAS No. 79-92-5. FEMA No. 2229. VIGON Item # 500049. Categories: Speciality Ingredients Suppliers, Flavors, Fragrances, Perfumers. |  America & Internationally |
| Camphene | Camphene. We stock inventory in warehouses throughout the United States, allowing us to serve customers in all regions in a timely and cost effective manner. |  California |
| Camphene Natural | Camphene Natural. CAS No. 79-92-5. FEMA No. 2229. Kosher: Y. VIGON Item # 508256. Categories: Speciality Ingredients Suppliers, Flavors, Fragrances, Perfumers, Aromatherapy, Essential Oils. | America & Internationally |
| Camphor | Camphor. We stock inventory in warehouses throughout the United States, allowing us to serve customers in all regions in a timely and cost effective manner. | California |
| Camphor | Camphor. Synonyms: (±)-Camphor, 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one. CAS No. 76-22-2. Pack Sizes: 100, 500 g in poly bottle. Product ID: CDC10-0191. Molecular formula: C10H16O. Category: Flavoring Chemical Agents. Product Keywords: Cosmetic Ingredients; Flavoring Chemical Agents; Camphor; CDC10-0191; 76-22-2; C10H16O; (±)-Camphor, 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one; 200-945-0; MFCD00074738; 76-22-2. Purity: 0.96. EC Number: 200-945-0. Solubility: Ethanol: soluble 1 g/L, clear, colorless. Quality Level: 100. Application: Camphor was used in the synthesis of single-walled nanotubes by chemical vapor deposition. It was used in two-phase based hollow fibre liquid-phase microextraction procedure for migration analysis of food packagings containing essential oils. Boiling Point: 204 °C (lit.). Melting Point: 175-177 °C (lit.). Product Description: Camphor is a novel carbon nanotube precursor. |  |
| Camphor | Camphor. Synonyms: camphanone;(1RS,4RS)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one;Caladryl;2-Kamfanon;2-CAMPHOR. CAS No. 76-22-2. Pack Sizes: 100, 500 g in poly bottle. Product ID: CDC10-0262. Molecular formula: C10H16O. Category: Cosmetic Plasticizers. Product Keywords: Cosmetic Ingredients; Cosmetic Plasticizers; Camphor; CDC10-0262; 76-22-2; C10H16O; camphanone; (1RS,4RS)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one; Caladryl; 2-Kamfanon; 2-CAMPHOR; 207-354-7; MFCD00064148; 76-22-2. Purity: 0.96. Color: Colorless or white. EC Number: 207-354-7. Physical State: Crystalline Powder. Solubility: Ethanol: soluble 1 g/L, clear, colorless. Application: Camphor was used in the synthesis of single-walled nanotubes by chemical vapor deposition. It was used in two-phase based hollow fibre liquid-phase microextraction procedure for migration analysis of food packagings containing essential oils. Boiling Point: 204ºC. Melting Point: 179ºC. Density: 0.992 g/cm3. Product Description: Kampfer is a waxy, flammable, white, or transparent solid with a strong aroma. It is a terpenoid with the chemical formula C10H16O. | |
| Camphor | Camphor appears as a colorless or white colored crystalline powder with a strong mothball-like odor. About the same density as water. Emits flammable vapors above 150°F. Used to make moth proofings, pharmaceuticals, and flavorings.;Camphor oil appears as a colorless liquid with a characteristic odor. Flash point 125°F. Insoluble in water and generally less dense than water. Vapors heavier than air.;D-camphor appears as colorless or white crystals. Sublimes. Flash point 149°F. Burns readily with a bright, smoky flame. Penetrating aromatic odor. Pungent, aromatic taste followed by a sensation of cold. (NTP, 1992);DryPowder; Liquid; PelletsLargeCrystals;COLOURLESS OR WHITE CRYSTALS WITH CHARACTERISTIC ODOUR.;White to gray translucent crystals or fused mass; Warm, minty, almost ethereal diffusive aroma;White to pale yellow crystalline solid, Camphoraceous aroma;Colorless or white crystals with a penetrating, aromatic odor.;Colorless or white crystals with a penetrating, aromatic odor. Group: Polymers. Product ID: 1,7,7-trimethylbicyclo[2.2.1]heptan-2-one. Molecular formula: 152.23g/mol. Mole weight: C10H16O;C10H16O;C10H16O. CC1(C2CCC1(C(=O)C2)C)C. InChI=1S/C10H16O/c1-9(2)7-4-5-10(9, 3)8(11)6-7/h7H, 4-6H2, 1-3H3. DSSYKIVIOFKYAU-UHFFFAOYSA-N. |  |
| Camphor | Camphor. CAS No: 76-22-2 |  Sarchem Laboratories New Jersey NJ |
| Camphor | Camphor ((±)-Camphor) is a topical anti-infective and anti-pruritic and internally as a stimulant and carminative. However, Camphor is poisonous when ingested. Antiviral, antitussive, and anticancer activities [1]. Camphor is a TRPV3 agonist [2]. Uses: Scientific research. Group: Natural products. Alternative Names: (±)-Camphor. CAS No. 76-22-2. Pack Sizes: 10 mM * 1 mL; 25 g; 50 g. Product ID: HY-N0808. | |
| Camphor | Kampfer is a waxy, flammable, white, or transparent solid with a strong aroma. It is a terpenoid with the chemical formula C10H16O. It is found in the wood of the Kampfer laurel (Cinnamomum camphora), a large evergreen tree found in Asia (particularly in Sumatra, Indonesia, and Borneo), and also of the unrelated Kapur tree, a tall timber tree from the same region. It also occurs in some other related trees in the laurel family, notably Ocotea usambarensis. The oil in rosemary leaves (Rosmarinus officinalis), in the mint family, contains 10 to 20%, Kampfer, while camphorweed (Heterotheca) only contains some 5%. Camphor can also be synthetically produced from the oil of turpentine. It is used for its scent, as an ingredient in cooking (mainly in India), as an embalming fluid, for medicinal purposes, and in religious ceremonies. A major source of camphor in Asia is camphor basil (the parent of African blue basil).The molecule has two possible enantiomers is shown in the structural diagrams. The structure on the left is the naturally occurring (R)-form, while its mirror image shown on the right is the (S)-form.Norcamphor is a Kampfer derivative with the three methyl groups replaced by hydrogen. Group: Inhibitors. Alternative Names: 1,7,7-Trimethyl-bicyclo[2.2.1]heptan-2-on. CAS No. 76-22-2. Molecular formula: C10H16O. Mole weight: 152.23. Appearance: Powder. Purity: 0.98. IUPACName: 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one. Canonica | |
| Camphor | Camphor is found in the wood of the camphor laurel (Cinnamomum camphora), a large evergreen tree found in East Asia. It can be used as a repellent, a plasticizer for nitrocellulose, a moth repellent, and an antimicrobial substance. Uses: Anti-infective agents, local. Synonyms: Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-; (±)-Camphor; 1,7,7-Trimethylbicyclo[2.2.1]-2-heptanone; 1,7,7-Trimethylnorcamphor; 2-Bornanone; 2-Camphanone; DL-Camphor; Alphanon; Borneo camphor; dl-Camphor; HCXL 8899; MeSH ID: D002164; Racemic camphor; Root bark oil; Spirit of camphor. Grades: ≥95%. CAS No. 76-22-2. Molecular formula: C10H16O. Mole weight: 152.23. | |
| Camphor | (±)-Camphor, has a strong aromatic odor. It is toxic to insects so it can be used as repellent. Camphor can also be used as a plasticizer for nitrocellulose, as a moth repellent, and as an antimicrobial substance.This compound is a contaminant of emerging concern (CECs). Group: Biochemicals. Alternative Names: (+/-)-Camphor; 1, 7, 7-Trimethylbicyclo[2. 2. 1]heptan-2-one; 1,7,7-Trimethylnorcamphor; 2-Bornanone; 2-Camphanone; Alphanon; Borneo camphor; DL-Camphor; Root bark Oil; Spirit of Camphor. Grades: Highly Purified. CAS No. 76-22-2. Pack Sizes: 1Kg. US Biological Life Sciences. | Worldwide |
| Camphor-10-sulfonic acid (β) | Camphorsulfonic acid is a organosulphur compound. Uses: Camphor-10-sulfonic acid (β) (csa) is extensively used as an acid catalyst. it can be used in a catalytic amount to protect hydroxyl groups as tetrahydropyranyl (thp) ethers using dihydropyran. it also catalyzes the protection of ketones as ketals. it is a useful catalyst for the intramolecular ring opening of epoxides. csa can also be used to catalyze nucleophile-promoted alkyne-iminium cyclization in the total synthesis of pumiliotoxin a. Group: Bioelectronic materials. Alternative Names: CSA. CAS No. 5872-8-2. Pack Sizes: 100, 500 g in glass bottle. Product ID: (7, 7-dimethyl-2-oxo-1-bicyclo[2. 2. 1]heptanyl)methanesulfonic acid. Molecular formula: 232.3. Mole weight: C10H16O4S. [H][C@@]12CC[C@@] (CS (O) (=O)=O) (C (=O)C1)C2 (C)C. 1S/C10H16O4S/c1-9(2)7-3-4-10(9, 8(11)5-7)6-15(12, 13)14/h7H, 3-6H2, 1-2H3, (H, 12, 13, 14)/t7-, 10-/m1/s1. MIOPJNTWMNEORI-GMSGAONNSA-N. | |
| camphor 5-monooxygenase | A heme-thiolate protein (P-450). Also acts on (-)-camphor and 1,2-campholide, forming 5-exo-hydroxy-1,2-campholide. Group: Enzymes. Synonyms: camphor 5-exo-methylene hydroxylase; 2-bornanone 5-exo-hydroxylase; bornanone 5-exo-hydroxylase; camphor 5-exo-hydroxylase; camphor 5-exohydroxylase; camphor hydroxylase; d-camphor monooxygenase; methylene hydroxylase; methylene monooxygenase; D-camphor-exo-hydroxylase; camphor methylene hydroxylase. Enzyme Commission Number: EC 1.14.15.1. CAS No. 9030-82-4. 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-0934; camphor 5-monooxygenase; EC 1.14.15.1; 9030-82-4; camphor 5-exo-methylene hydroxylase; 2-bornanone 5-exo-hydroxylase; bornanone 5-exo-hydroxylase; camphor 5-exo-hydroxylase; camphor 5-exohydroxylase; camphor hydroxylase; d-camphor monooxygenase; methylene hydroxylase; methylene monooxygenase; D-camphor-exo-hydroxylase; camphor methylene hydroxylase. Cat No: EXWM-0934. | |
| Camphor Monobromated | Camphor Monobromated. CAS No: 10293-06-8 | Sarchem Laboratories New Jersey NJ |
| CAMPHOR OIL | Camphor appears as a colorless or white colored crystalline powder with a strong mothball-like odor. About the same density as water. Emits flammable vapors above 150°F. Used to make moth proofings, pharmaceuticals, and flavorings.;Camphor oil appears as a colorless liquid with a characteristic odor. Flash point 125°F. Insoluble in water and generally less dense than water. Vapors heavier than air.;D-camphor appears as colorless or white crystals. Sublimes. Flash point 149°F. Burns readily with a bright, smoky flame. Penetrating aromatic odor. Pungent, aromatic taste followed by a sensation of cold. (NTP, 1992);DryPowder; Liquid; PelletsLargeCrystals;COLOURLESS OR WHITE CRYSTALS WITH CHARACTERISTIC ODOUR.;White to gray translucent crystals or fused mass; Warm, minty, almost ethereal diffusive aroma;White to pale yellow crystalline solid, Camphoraceous aroma;Colorless or white crystals with a penetrating, aromatic odor.;Colorless or white crystals with a penetrating, aromatic odor. Group: Polymers. Product ID: 1,7,7-trimethylbicyclo[2.2.1]heptan-2-one. Molecular formula: 152.23g/mol. Mole weight: C10H16O;C10H16O;C10H16O. CC1(C2CCC1(C(=O)C2)C)C. InChI=1S/C10H16O/c1-9(2)7-4-5-10(9, 3)8(11)6-7/h7H, 4-6H2, 1-3H3. DSSYKIVIOFKYAU-UHFFFAOYSA-N. | |
| Camphor Oil White | Camphor Oil White. CAS No. 8008-51-3. FEMA No. 2231. Kosher: Y. VIGON Item # 502149. Categories: Speciality Ingredients Suppliers, Flavors, Fragrances, Perfumers, Cosmetics. | America & Internationally |
| Camphor Powder Natural | Camphor Powder Natural. CAS No. 464-49-3. FEMA No. 2230. VIGON Item # 505010. Categories: Speciality Ingredients Suppliers, Flavors, Fragrances, Perfumers, Aromatherapy, Essential Oils. | America & Internationally |
| Camphor Powder Synthetic | Camphor Powder Synthetic. CAS No. 464-49-3. FEMA No. 2230. VIGON Item # 500646. Categories: Speciality Ingredients Suppliers, Flavors, Fragrances, Perfumers. | America & Internationally |
| Camphorquinone | Camphorquinone. CAS No: 10373-78-1 | Sarchem Laboratories New Jersey NJ |
| Camphorquinone-10-sulfonic acid hydrate | Camphorquinone-10-sulfonic acid hydrate. Group: Biochemicals. Alternative Names: (1S, 4S)-7, 7-dimethyl-2, 3-dioxobicyclo[2. 2. 1]heptane-1-methanesulfonic acid; CQS-OH. Grades: Highly Purified. CAS No. 73413-79-3. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C10H16O6S. US Biological Life Sciences. | Worldwide |
| Camphorquinone-10-sulfonyl chloride | Camphorquinone-10-sulfonyl chloride. Group: Biochemicals. Alternative Names: 7,7-Dimethyl-2,3-dioxo-bicyclo[2.2.1]heptane-1-methanesulfonyl chloride. Grades: Highly Purified. CAS No. 82594-19-2. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. Molecular Formula: C10H13ClO4S. US Biological Life Sciences. | Worldwide |
| Camphorquinone-10-sulfonylnorleucine | Camphorquinone-10-sulfonylnorleucine. Group: Biochemicals. Alternative Names: (1S)-N-[[(7, 7-Dimethyl-2, 3-dioxobicyclo[2. 2. 1]hept-1-yl)methyl]sulfonyl]-L-norleucine; CQS-NLE-OH. Grades: Highly Purified. CAS No. 73413-80-6. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C16H25NO6S. US Biological Life Sciences. | Worldwide |
| Camphorsulfonic acid Ethyl Ester | Camphorsulfonic acid Ethyl Ester. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: ethyl (7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonate. Molecular Formula: C12H20O4S. Mole Weight: 260.35. Catalog: APB04513. | |
| Camphorsulfonic acid Methyl Ester | Camphorsulfonic acid Methyl Ester. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: methyl (7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonate. Molecular Formula: C11H18O4S. Mole Weight: 246.32. Catalog: APB04514. | |
| Camphorsultam | Heterocyclic Organic Compound. CAS No. 108488-77-7. Purity: 0.96. Catalog: ACM108488777. | |
| Camphor, Synthetic, Blocks | Camphor appears as a colorless or white colored crystalline powder with a strong mothball-like odor. About the same density as water. Emits flammable vapors above 150°F. Used to make moth proofings, pharmaceuticals, and flavorings.;Camphor oil appears as a colorless liquid with a characteristic odor. Flash point 125°F. Insoluble in water and generally less dense than water. Vapors heavier than air.;D-camphor appears as colorless or white crystals. Sublimes. Flash point 149°F. Burns readily with a bright, smoky flame. Penetrating aromatic odor. Pungent, aromatic taste followed by a sensation of cold. (NTP, 1992);DryPowder; Liquid; PelletsLargeCrystals;COLOURLESS OR WHITE CRYSTALS WITH CHARACTERISTIC ODOUR.;White to gray translucent crystals or fused mass; Warm, minty, almost ethereal diffusive aroma;White to pale yellow crystalline solid, Camphoraceous aroma;Colorless or white crystals with a penetrating, aromatic odor.;Colorless or white crystals with a penetrating, aromatic odor. Group: Plasticizers. CAS No. 76-22-2. Product ID: 1,7,7-trimethylbicyclo[2.2.1]heptan-2-one. Molecular formula: 152.23g/mol. Mole weight: C10H16O;C10H16O;C10H16O. CC1(C2CCC1(C(=O)C2)C)C. InChI=1S/C10H16O/c1-9(2)7-4-5-10(9, 3)8(11)6-7/h7H, 4-6H2, 1-3H3. DSSYKIVIOFKYAU-UHFFFAOYSA-N. | |
| Camphor, Synthetic, USP | Camphor appears as a colorless or white colored crystalline powder with a strong mothball-like odor. About the same density as water. Emits flammable vapors above 150°F. Used to make moth proofings, pharmaceuticals, and flavorings.;Camphor oil appears as a colorless liquid with a characteristic odor. Flash point 125°F. Insoluble in water and generally less dense than water. Vapors heavier than air.;D-camphor appears as colorless or white crystals. Sublimes. Flash point 149°F. Burns readily with a bright, smoky flame. Penetrating aromatic odor. Pungent, aromatic taste followed by a sensation of cold. (NTP, 1992);DryPowder; Liquid; PelletsLargeCrystals;COLOURLESS OR WHITE CRYSTALS WITH CHARACTERISTIC ODOUR.;White to gray translucent crystals or fused mass; Warm, minty, almost ethereal diffusive aroma;White to pale yellow crystalline solid, Camphoraceous aroma;Colorless or white crystals with a penetrating, aromatic odor.;Colorless or white crystals with a penetrating, aromatic odor. Group: Plasticizers. CAS No. 76-22-2. Product ID: 1,7,7-trimethylbicyclo[2.2.1]heptan-2-one. Molecular formula: 152.23g/mol. Mole weight: C10H16O;C10H16O;C10H16O. CC1(C2CCC1(C(=O)C2)C)C. InChI=1S/C10H16O/c1-9(2)7-4-5-10(9, 3)8(11)6-7/h7H, 4-6H2, 1-3H3. DSSYKIVIOFKYAU-UHFFFAOYSA-N. | |
| cAMPS-Rp, triethylammonium salt | cAMPS-Rp, triethylammonium salt. Group: Biochemicals. Grades: Purified. CAS No. 151837-09-1. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| cAMPS-Sp, triethylammonium salt | cAMPS-Sp, triethylammonium salt. Group: Biochemicals. Grades: Purified. CAS No. 93602-66-5. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
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