Toxicology

<p>Applications Flucarbazone-sodium is a herbicide.<br>References Eliason, R., et al.: Weed Sci., 52, 857 (2004);<br></p>

<p>Applications Picloram is used as a herbicide. Studies show that Picloram can reduce seed germination rate and vigor as well as seedling growth in Bidens pilosa L.<br>References Freitas, M.R., et al.: RSC Adv., 5, 7547 (2015); Tian, X., et al.: Nongyao, 53, 485 (2014)<br></p>

<p>Applications Mono N-Desmethyl Disperse Polyester Dark Blue is a disperse dye for synthetic polyester fibers. It has good heat and light resistance and is used for thermal transfer recording.<br>References Peters A. T., et al.: J. Soc. Dyers Colour, 108(7-8), 344-8 (1992)<br></p>

<p>Applications FOY 251-D4 is a labelled analogue of FOY 251 (F754500).<br></p>

<p>Stability Hygroscopic<br>Applications Carboprost Tromethanimine is the salt of Carboprost (C177580), an analog of prostaglandin F2α.<br>References Weeks, J.R., et al.: J. Pharmacol. Exp. Ther., 67, 186 (1973), Csapo, A.I., et al.: Prostaglandins, 18, 479 (1979), Schwallie, P.C., et al.: J. Reprod. Med., 23, 289 (1979), Mapa, M.P., et al.: Int. J. Gynaecol. Obstet., 20, 125 (1982),<br></p>

<p>Stability Hygroscopic<br>Applications Chlorhexidine Digluconate Impurity K was found in a study of the kinetics of chlorhexidine hydrolysis.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Zong, Z., Lee, E.K.: J. Pharm. Sci., 101, 2417 (2012)<br></p>

<p>Stability Hygroscopic<br>Applications A metabolite of Lamivudine (L172500).<br>References Burgess, K., et al.: Chem. Rev., 100, 2047 (2000), Gallois-Montbrun, S., et al.: Biochem. Pharmacol., 68, 1749 (2004),<br></p>

<p>Applications It is a peroxisome proliferator-activated receptor (PPAR) α/γ dual agonist.<br>References Barlocco, D., et al.: Curr. Opin. Invest. Drugs, 6, 427 (2005), Devasthale, P.V., et al.: J. Med. Chem., 48, 2248 (2005), Kendall, D.M., et al.: Diabetes care, 29, 1016 (2006),<br></p>

<p>Applications Shows antioxidant effects. Antiseptic.<br>References Wong, S., et al.: Clin. Chem., 33, 214 (1987), Daood, H., et al.: Food Chem., 55, 365 (1996), Zainol, M., et al.: Food Chem., 81, 575 (2003),<br></p>

<p>Impurity Vancomycin Impurity<br>Applications An impurity in Vancomycin.A representative lot was 75% by HPLC with less than 0.1% vancomycin.<br>References Marshall, F.J., et al.: J. Med. Chem., 8, 18 (1965), Sheldrick, G.M., et al.: Nature, 271, 223 (1987), Dutca-Melan, S., et al.: J. Clin. Microbiol., 33, 24 (1995),<br></p>

<p>Applications Diuron is a phenyl urea herbicide (1,2). Pre-emergent herbicide which may find its way into aquatic environments, and consumable fruit/vegetation (3,4). Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References 1. Noseworthy, J. et al.: Weed. Tech. 2010 Jul:24(1) pp64-702. Armenta, S. et al.: Anal. Bioanal. Chem. 2010 May;397(1):297-308.3. Neuwoehner, J. et al.: Aquat. Toxicol. 2010 Apr 1;97(1):58-67.4. Wong, J. et al.: J. Agric. Food. Chem. 2010 May 26;58(10):5897-9034<br></p>

<p>Applications Terbuthylazine-(ethyl-d5) is the deuterized or labeled form of Terbuthylazine (T110500), which is a triazine herbicide.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Schenck, F., et al.: Bull Environ. Contam. Toxicol., 73, 24 (2004)<br></p>

<p>Stability Moisture sensitive<br>Applications Fenclofenac Glucuronide is a metabolite of Fenclofenac, a non-steroidal anti-inflammatory agent. Mild immunosuppressive agent.<br>References Lim, C. et al.: Metabolism, 44, 1008 (1995); Spiers, E. et al.: Int. J. Immunopharmacol., 15, 865 (1993);<br></p>

<p>Applications Triflumuron is a benzoylphenylurea insecticide. Triflumuron is a chitin synthesis inhibitor used to control insects pests such as mosquitos and flies.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Schaefer, C.H.: J. Econ. Entomol., 71, 427 (1978); Zoebelein, G. et al.: Zeitsch. Angew. Entomol., 89, 289 (1980); Chang, S.C.: J. Econ. Entomol., 77, 479 (1979);<br></p>

<p>Stability Volatile<br>Applications N-Methyl-N-formylhydrazine is a substituent used in the synthesis of Marbofloxacin (M197000), a fluorinated quinolone antibacterial agent.<br>References Gruet, P., et al.: Vet. Rec., 140, 199 (1977), Lefebvre, H.P., et al.: J. Vet. Pharmacol. Ther., 21, 453 (1998),<br></p>

<p>Applications A classical β-adrenergic agonist in retina in interlaboratory study.<br>References Horwitz, W., et al.: Anal. Chem., 54, 67 (1982), Gowik, P., et al.: Analyst, 125, 1103 (2000),<br></p>

<p>Applications Labelled Levamisole. Biological response modifier with anthelmintic activity. Anthelmintic (nematodes); immunomodulator.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Thienpoint, D., et al.: Nature, 209, 1084 (1966), Bullock, M.W., et al.: J. Med. Chem., 11, 169 (1968), Miller, M.J., et al.: Drugs, 20, 122 (1980), Stevenson, H.C., et al.: J. Clin. Oncol., 9, 2052 (1991), Amery, W.K., et al.: Int. J. Immunopharmacol., 14, 481 (1992),<br></p>

<p>Applications Controlled substance (depressant). Sedative; hypnotic.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Horwitz, et al.: Drug Metab. Dispos., 8, 77 (1980),<br></p>

<p>Impurity Fusidic Acid EP Impurity G<br>Applications 3-Keto Fusidic Acid (Fusidic Acid EP Impurity G) is a metabolite of Fusidic Acid.<br>References Godtfredsen, W.O., et al.: J. Med. Chem., 9, 15 (1966), Perry, M.J., et al.: J. Antibiot., 36, 1659 (1983),<br></p>

<p>Applications Radioactive imaging agent.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Subramanian, G., et al.: J. Nucl. Med., 16, 744 (1975), Rosenthall, L., et al.: Clin. Nucl. Med., 2, 232 (1977), Bull, U., et al.: Br. J. Radiol., 50, 629 (1977), Garty, I., et al.: Clin. Nucl. Med., 14, 515 (1989)<br></p>

<p>Applications N-Demethyl-N-(ethylsuccinyl) Erythromycin is an impurity of Erythromycin (E649950), an antibiotic that has a wider spectrum than penicillin (P223500).<br>References Koch, W.L., et al.: Anal. Profiles Drug Subs., 8, 157 (1979),<br></p>

<p>Applications Labelled Amprenavir, a selective HIV protease inhibitor. An analogue of Ritonavir.<br>References Adkins, J.C., et al.: Drugs, 55, 837 (1998)<br></p>

<p>Applications Digoxin derivative, a cardiotonic glycosides steroid.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Yoshida, F., et al.: J. Med. Chem., 43, 2575 ( 2000), Turner, J., et al.: Pharm. Res., 21, 68 (2004), Wang, J., et al.: Anal. Chim. Acta, 601, 156 (2007),<br></p>

<p>Applications Ethametsulfuron-methyl is a regulator of the early steps of complement activation on mucosal surfaces. It can be used in combination treatment of ohmic heating with various essential oil components for inactivation of food-​borne pathogens in buffered peptone water and salsa.<br>References Kim, S. S., et al.: Food Control, 80, 29 (2017); Reichhardt, M. P., et al.: Front Immunol, 7, 85 (2016)<br></p>

<p>Applications Pyribenzoxim can be used in biological study of production of acetolactate synthase inhibitor herbicide tolerant Brassica napus mutants.<br>References Ruiter, R., et al.: U.S. Pat. Appl. Publ., US 20150089682 A1 20150326 (2015)<br></p>

<p>Stability Hygroscopic<br>Applications A medicinal agent for treating viral infections.<br>References Chiou, W., et al.: J. Pharm. Sci., 60, 1281 (1971), Ford, J., et al.: J. Pharm. Pharmacol., 31, 726 (1979), Tamblyn, S., et al.: Eur. J. Epidemiol., 10, 503 (1994), Suzuki, H., et al.: Chem. Pharm. Bull., 45, 1688 (1997),<br></p>

<p>Applications De-O-ethoxy Tamsulosin is a derivative of Tamulosin (T006350), a specific α1-adrenoceptor antagonist. It is used in the treatment of benign prostatic hypertrophy.<br>References Kawabe, K., et al.: J. Urol., 144, 908 (1990), Abrams, P., et al.: Br. J. Urol., 76, 325 (1995), Michel, M.C., Expert Opin. Pharmacother., 5, 151 (2004),<br></p>

<p>Stability Hygroscopic<br>Applications Abacavir 5’-β-D-Glucuronide is a metabolite of Abacavir (A105000). Abacavir is a carbocyclic 2'-deoxyguanosine nucleoside reverse transcriptase inhibitor and an anti-HIV drug used to treat HIV infection (1). Intracellular enzymes convert Abacavir to its active form, carbovir-triphosphate (CBV-TP), which then selectively inhibits HIV reverse transcriptase by incorporating into viral DNA (2). Abacavir is metabolized in the liver by uridine diphosphate glucuronyltransferase and alcohol dehydrogenase resulting in inactive glucuronide and carboxylate metabolites, respectively.<br>References (1) Jackson, A., et al.: Antivir Ther. 17, 19 (2012) (2) Yuen, G. J., et al.: Clin Pharmacokinet. 47, 351 (2008)<br></p>

<p>Stability Light Sensitive<br>Applications Labelled Eugenol is a dental compound which shows cytotoxicity to human oral squamous cell carcinoma and oral cells. When glucosylated, this compound exhibits anti-inflammatory activity.<br>References Koh, T. et al.: In Vivo, 27, 85 (2013); Zhang, P. et al.: Arch. Pharm. Res., 36, 109 (2013);<br></p>

<p>Stability Hygroscopic<br>Applications 2-Hydroxyethanephosphonic acid is an substrate used in the study of 2-hydroxyethylphosphonate dioxygenase reaction mechanism. 2-Hydroxyethanephosphonic Acid is also a required intermediate in labelled Fosfomycin (F727502) biosynthesis.<br>References Hirao, H., et al.: J. Am. Chem. Soc., 133, 14550 (2011); Hidaka, T., et al.: J. Antibiot., 45, 1008 (1992); Patel, S., et al.: Drugs, 53, 637 (1997); Ribes, S., et al.: J. Antimicrob. Chemother., 57, 931 (2006);<br></p>

<p>Applications N-(Carboxymethyl)amphetamine Hydrochloride is a synthetic amphetamine-class analyte with potential pharmaceutical properties.<br>References Seiler, N. et al.: Tetrahedron Lett., 38, 4603 (1966);<br></p>

<p>Stability Hygroscopic<br>Applications Isotope labelled 1,6-Anhydro-β-D-glucopyranose (A648100), an compound that have been proven to be a valuable synthon for the preparation of various biologically important and structurally diverse products (e.g. rifamycin S, indanomycin, thromboxane B2, (+)-biotin, tetrodotoxin, quinone, and macrolide antibiotics) as well as for modified sugars.<br>References Fraser-Reid, B., et al. J. Am. Chem. Soc. 106, 731 (1984); Edwards, M.P., et al. J. Org. Chem. 49, 3503 (1984); Kelly, A.G., and Roberts, J.S. J. Chem. Soc., Chem. Commun. 228, (1980); Ogawa, T., et al. Carbohydr. Res. 57, C31 (1977); Isobe, M., et al. Tetrahedron Lett. 28, 6485 (1987);<br></p>

<p>Applications Propazine<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>

<p>Applications Florasulam is a triazolopyrimidine sulfonamide compound that is used as a post emergence herbicide. Florasulam is often used to control dandelion populations in wheat fields.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Krieger, M., et al.: J. Agr. Food Chem., 48, 3710 (2000); Li, Z., et al.: Bull. Environ. Cont. Toxicol., 90, 280 (2013)<br></p>

<p>Applications An antimalarial.<br>References Natarajan, L., et al.: Arzneim.-Forsch., 22, 1230 (1972), Kracmer, J., et al.: Pharmazie, 29, 773 (1974), Ahmad, I., et al.: Anal. Profiles Drug Subs., 21, 43 (1992),<br></p>

<p>Stability Hygroscopic<br>Applications A new analgesic.<br>References de Julian-Ortiz, J., et al.: J. Med. Chem., 42, 3308 (1999), Roy, K., et al.: Bioorg. Med. Chem., 12, 745 (2004), Garcia-Garcia, A., et al.: J. Antimicrob. Chemother., 53, 65 (2004),<br></p>

<p>Applications Quinolone antibacterial. This compound is a contaminant of emerging concern (CECs).<br>References DiCarlo, et al.: Arch. Biochem. Biophys., 127, 503 (1968), Crew, et al.: Xenobiotica, 1, 193 (1971), Wright, H.T., et al.: Science, 213, 455 (1981),<br></p>

<p>Stability Light Sensitive<br>Applications A labelled metabolite of Rifampicin.<br>References Blumenfeld,O.O., et al.: J. Biol. Chem., 236, 2472 (1961), Cowxan, R.A., et al.: Biochem. Biophys. Res. Commun, 23, 799 (1966)<br></p>

<p>Applications trans-Abacavir Dihydrochloride is an impurity of Abacavir. Abacavir (A104990) is a carbocyclic 2'-deoxyguanosine nucleoside reverse transcriptase inhibitor and an anti-HIV drug used to treat HIV infection (1). Intracellular enzymes convert Abacavir to its active form, carbovir-triphosphate (CBV-TP), which then selectively inhibits HIV reverse transcriptase by incorporating into viral DNA (2). Abacavir is metabolized in the liver by uridine diphosphate glucuronyltransferase and alcohol dehydrogenase resulting in inactive glucuronide and carboxylate metabolites, respectively.<br>References (1) Jackson, A., et al.: Antivir Ther. 17, 19 (2012) (2) Yuen, G. J., et al.: Clin Pharmacokinet. 47, 351 (2008)<br></p>

<p>Impurity Clarithromycin EP Impurity I<br>Applications De(cladinosyl) Clarithromycin (Clarithromycin EP Impurity I) is an impurity of Clarithromycin (C559750). De(cladinosyl) Clarithromycin showed significantly potent antibacterial activity against community acquired respiratory pathogens.<br>References Morimoto, S., et al.: J. Antibiot., 37, 187 (1984), Buxbaum, A., et al.: J. Antimicrob. Chemother., 52, 371 (2003), Westphal, J., et al.: Br. J. Clin. Pharmacol., 50, 285 (2000), Ma, Z., et al.: J. Med. Chem., 44, 4137 (2001),<br></p>

<p>Impurity Hydrochlorothiazide EP Impurity C<br>Applications N-[[7-(Aminosulfonyl)-6-chloro-2,3-dihydro-1,1-dioxo-4H-1,2,4-benzothiadiazin-4-yl]methyl]-6-chloro-3,4-dihydro-1,1-dioxo-2H-1,2,4-benzothiadiazine-7-sulfonamide (Hydrochlorothiazide EP Impurity C) is an impurity in bulk Hydrochlorothiazide. Dimer Impurity C.<br>References Daniels, S.L., et al.: J. Pharm. Sci., 70, 211 (1981), Fang, X., et al.: Pharm. Res., 14, 691 (1997),<br></p>

<p>Impurity Moxifloaxacin EP Impurity A<br>Stability Hygroscopic<br>Applications 8-Desmethoxy-8-fluoro Moxifloxacin (Moxifloaxacin EP Impurity A) is an impurity of Moxifloxacin (M745000).<br>References Martel, A., et al.: Drugs Fut., 22, 109 (1997), Tobin, C., et al.: J. Antimicrob. Chemother., 42, 278 (1998),<br></p>

<p>Applications Deuterated Mycopheolate Mofetil, an immunosuppressant.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Lee, W.A., et al.: Pharm. Res., 7, 161 (1990), Bullingham, R.E.S., et al.: Transplant. Proc., 28, 925 (1996), Keown, P.A., et al.: Transplantation, 61, 1029 (1996),<br></p>

<p>Stability Moisture Sensitive<br>Applications Tetramethylphosphorodiamidic Fluoride is a type of pesticide.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Hayat, K., et al.: Afr. J. Environ., 4, 666 (2010)<br></p>

<p>Applications Labelled Piracetam (P500800). Nootropic.<br>References Gobert, J., et al.: J. Pharm. Belg., 27, 281 (1972), Oosterveld, W.J., et al.: Arzneim.-Forsch., 30, 1947 (1980), Chouinard, G., et al.: Psychopharmacol. Bull., 17, 129 (1981),<br></p>

<p>Applications WP 155, is a pesticide that has mutagenic effect on Saccharomyces cerevisiae and Aspergillus nidulans, which was verified by comparing with standard mutagen methylmethansulfonate.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References De Bertoldi, M., et al.: Environ. Mutagen., 2, 359 (1980)<br></p>

<p>Applications Labelled Dimethomorph (D460530). Agricultural fungicide.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Lu, X., et al.: Phytopathol., 100, 1162 (2010), Schafer, R., et al.: Environ. Sci. Technol., 45, 1665 (2011),<br></p>

<p>Stability Light Sensitive, Temperature Sensitive<br>Applications Xanthophyll is one of the most widespread carotenoid alcohols in nature. Originally isolated from egg yolk, also isolated by chromatography from nettles, algae, and petals of many yellow flowers.<br>References van het Hof, K., et al.: J. Nutr., 130, 503 (2000), Cooper, D., et al.: J. Nutr., 134, 221S (2004), Faulks, R., et al.: Biochim. Biophys. Acta, 1740, 95 (2005), Rao, A., et al.: Pharmacol. Res., 55, 207 (2007), Tuberoso, C., et al.: Food Chem., 103, 149 (2007),<br></p>

<p>Stability Hygroscopic<br>Applications Plerixafor is a hematopoietic stem cell (HSC) mobilizer that inhibits the CXCR4 chemokine receptor and blocks binding of its ligand, stromal cell-derived factor-1-α (SDF-1-α). This agent was approved on Dec. 15, 2008, as treatment in combination with granulocyte-colony stimulating factor (G-CSF) to mobilize HSCs to the peripheral blood for collection and subsequent autologous transplantation in patients with non-Hodgkin's lymphoma (NHL) and multiple myeloma (MM). Selective CXCR4 antagonist.<br>References Xie, T., et al.: Science, 290, 328 (2000), Leone, D., et al.: J. Pharmacol. Exp. Ther., 305, 1150 (2003), Chigaev, A., et al.: J. Immunol. 178, 6828 (2007), Kiel, M., et al.: Cell Stem Cell, 1, 204 (2007),<br></p>

<p>Applications Bisphenol AF-13C12 is the isotope labelled analog of Bisphenol AF (2,2-Bis-(4-hydroxyphenyl)hexafluoropropane). 2,2-Bis-(4-hydroxyphenyl)hexafluoropropane acts as an endocrine-disrupting chemical (EDC), activating estrogen through the estrogen receptor ERα. It is a full agonist for the estrogen receptor.<br>References Matsushima, A. et al.: Environ. Health, Perspect. 118, 1267 (2010);<br></p>

<p>Applications A labelled form of Ethoprophos (E890530), which is an organophosphate non-systemic nematicide and soil insecticide.<br>References Lehotay, S. J.; Chromatographia (2018).<br></p>

<p>Impurity Ritonavir EP Impurity L<br>Applications Desthiazolylmethyl Ritonavir (Ritonavir EP Impurity L) is an analogue of the selective HIV protease inhibitor Ritonavir (R535000). It is a COVID19-related research product.<br>References Brittain, H., et al.: Pharm. Res., 8, 963 (1991), Sham, H., et al.: J. Med. Chem., 39, 392 (1996), Phadnis, N., et al.: J. Pharm. Sci.,86, 1256 (1997), Bauer, J., et al.: Pharma. Res., 18, 859 (2001),<br></p>

<p>Stability Hygroscopic<br>Applications Pizotifen Malate is an anti migraine drug.<br>References Serna-Jimenez. et al.,Int. J. Pharm. 492, 223-232(2015);<br></p>

<p>Applications Flutriafol is a systemic fungicide of the triazole class. Flutriafol has broad spectrum fungicidal activity and is used to control effectively cereal powdery mildew, cloud disease, leaf spot disease and rust disease.<br>References Gozzo, F. et al.: Pest. Biochem. Physiol., 40, 68 (1991); Cao, W. et al.: Jing. Huag. Zhong., 36, 33 (2006); Evans, V.J. et al.: BCPC Conf. Pests Dis., 1, 511 (2000);<br></p>

<p>Applications Ambroxol O-glucuronide is a metabolite of Ambroxol (A575900, HCl salt), a bronchosecretolytic drug.<br>References Jauch, R., et al.: Arzneim-Forsch., 13, 474 (1963)<br></p>

<p>Applications Influenza viral neuraminidase inhibitor; structural analog of the sialic acid. Antiviral.<br>References Woods, J.M., et al.: Antimicrob. Agents Chemother., 37, 1473 (1993), Pegg, M.S., et al.: Biochem. Mol. Biol. Int., 32, 851 (1994), Monto, A.S., et al.: J. Am. Med. Assoc., 282, 31 (1999),<br></p>

<p>Stability Hygroscopic<br>Applications 3-Hydroxybutyrylcarnitine is a reagent used to study acylcarnitine profile in thyroid disease.<br>References Wong, S., et al.: Clinical Biochem., 46, 180 (2013); Alu, F., et al.: Heredity, 110, 253 (2013); Adam, B., et al.: Clinical Biochem., 44, 1445 (2011)<br></p>

<p>Applications 2,3,4-Trihydroxybenzophenone-2’,3’,4’,5’,6’-d5 is the isotope labelled analog of 2,3,4-Trihydroxybenzophenone; a trihydroxy derivative of Benzophenone (B204980) which is a compound used in the manufacturing of antihistamines, hypnotics, and insecticides.<br>References Wallace, W., et al.: Environ. Toxicol. Chem., 19, 962 (2000); Hayashi, T., et al.: Toxicol. Lett., 167, 1 (2006); Bechard, K., et al.: Aquat. Toxicol., 90, 310 (2008)<br></p>

<p>Applications Undecanoic-d21 Acid (CAS# 60658-40-4) is a useful isotopically labeled research compound.<br></p>

<p>Applications Potent inhibitor of Phosphatidylinositol 3-kinase (PI3K)<br></p>

<p>Applications Albuterol-d4, is the labeled analogue of Albuterol (A514500), a β2-adrenoceptor agonist, bronchodilator, and tocolytic.<br>References Brittain, R.T., et al.: Nature, 219, 862 (1968), Cullum, V.A, et al.: Br. J. Pharmacol. 35, 141 (1969), Martin, L.E., et al.: Eur. J. Pharmacol., 14, 183 (1971), Aboul-Enein, H.Y., Anal. Profiles Drug Subs., 10, 665 (1981)<br></p>

<p>Applications An intermediate of Indapamide (I500100), as bactericide, disinfectant, and antiseptic.<br>References Kumar, P., et al.: Arch. Pharma., 316, 759 (1983), Rival, Y., et al.: Eur. J. Med. Chem., 26, 13 (1991),<br></p>

<p>Applications Ginsenoside Rh4 possesses inhibitory and antifungal activity.<br>References Xue, P., et al: RSC Adv., 7, 10939-10946 (2017)<br></p>

<p>Applications Ethionamide-d3 is the isotope labelled analogue of Ethionamide (E890420), a antibacterial (tuberculostatic) agent.<br>References Banerjee, A., et al.: Science, 263, 227 (1994), Newton, G., et al.: J. Bacteriol., 178, 1990 (1996), Baulard, A., et al.: J. Biol. Chem., 275, 28326 (2000), Koledin, T., et al.: Arch. Microbiol., 178, 331 (2002), Cardoso, R., et al.: Antimicrob. Agents Chemother., 48, 3373 (2004),<br></p>

<p>Applications Broad spectrum third generation cephalosporin antibiotic.<br>References Wise, R., et al.: Antimicrob. Agents Chemother., 14, 807 (1978), Muhtadi, F.J., et al.: Anal. Profiles Drug Subs., 11, 139 (1982),<br></p>

<p>Applications ent-Entecavir is an enantiomeric impurity of the antiviral drug Entecavir (E558900).<br>References Ruediger, E. et al.: Tetrahed. Lett., 45, 739 (2004): Bisacchi, G.S. et al.: Bioorg. Med. Chem. Lett., 7, 127 (1997);<br></p>

<p>Applications Isotope labelled analog of Gamithromycin (G195000), a macrolide compound which is known to have antibacterial activity, and is useful in the therapy of bacterial infections in mammals. Antibiotic.<br>References Broto, P., et al.: Eur. J. Med. Chem., 19, 71 (1984), Farrar, V., et al.: J. Med. Chem., 36, 3517 (1993), Clark, D., et al.: J. Pharm. Sci., 88, 807 (1999),<br></p>

<p>Impurity Fusidic Acid EP Impurity H<br>Applications 11-Keto Fusidic Acid (Fusidic Acid EP Impurity H) is a metabolite of Fusidic Acid.<br>References Godtfredsen, W.O., et al.: J. Med. Chem., 9, 15 (1966), Perry, M.J., et al.: J. Antibiot., 36, 1659 (1983),<br></p>

<p>Applications Labelled Zephirol. Quaternary ammonium composition to treat herpes, pseudomonas, staph, hepatitis and other infectious diseases.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Berr, S., et al.: J. Phys. Chem., 91, 4760 (1987), Jones, M., et al.: Eur. J. Pharm. Biopharm., 48, 101 (1999), Okano, L., et al.: Langmuir, 16, 3119 (2000),<br></p>

<p>Applications An organophosphate pesticide that is an inhibitor of acetylcholinesterase (AChE).<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Yan, D. et al.: Zhong. Huan. Kex., 26, 364 (2006); Wood, S.J. et al.: Pest. Sci., 32, 485 (1991);<br></p>

<p>Applications Pentachloronitrobenzene is used in the synthesis of chlorodibenzo-p-dioxins for toxilogical studies. Its a pesticide used in the protection of crops from fungal bacterium. Useful in cannabis testing kits as a component of pesticide mixes (P698235).<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Munoz, E. et al.: J. AOAC Int., 95, 1777 (2012); Pohland, A. et al.: J. Agri. Food Chem., 20, 1093 (1972);<br></p>

<p>Impurity Ribavirin EP Impurity D<br>Applications N-Des-1-β-D-ribofuranosyl Ribavirin (Ribavirin EP Impurity D) is an impurity in the synthesis of Ribavirin (R414475), a purine nucleoside analog; inhibits inosine monophosphate dehydrogenase (IMPDH). Used as an antiviral agent.This compound is suitable for pyruvate dehydrogenase (PDH) related research.<br>References Fernandez, H., et al.: Eur. J. Epidemiol., 2, 1 (1986), Liao, H.J. and Stollar, V.: Antiviral Res., 22, 285 (1993), Honda, Y., et al.: Antimicrob. Agents Chemother., 38, 653 (1994), Reichard, O., et al.: Lancet, 351, 83 (1998)<br></p>

<p>Stability Hygroscopic<br>Applications Phenethicillin is a semisynthetic penicillin based β-lactam antibiotic and are used in the treatment of bacterial infections caused by susceptible, usually Gram-positive bacteria.<br>References Lucien, C., et al.: Can. med. Assoc. J., 84, 535 (1961); Timmers, G.J., et al.: Clin. Microbiol. Infect., 13, 497 (2007);<br></p>

<p>Applications A phosphocholine ester metabolite of the immunosuppressant macrolide SDZ RAD (also known as Everolimus E945400) which is an analog of the parent drug Rapamycin (R124000).<br>References Zollinger, M. et al.: Drug. Metab. Disp., 36, 1457 (2008); Kovarik, J. M., et al.: Clin. Pharmacol. Ther., 69, 48 (2001);<br></p>

<p>Stability Hygroscopic<br>Applications Octenidine is an antiseptic (topical). Octenidine is a cationic surfactant and bis-(dihydropyridinyl)-decane derivative.<br>References Slee, A.M., et al.: Antimicrob. Agents Chemother., 23, 531 (1983), Ghannoum, M.A., et al.: J. Antimicrob. Chemother., 25, 237 (1990), Allen, M., et al.: Microbiology, 152, 989 (2006), Ojha, A., et al.: Mol. Microbiol., 66, 468 (2007),<br></p>

<p>Applications A red Cy3-based biarsenical fluorescent probe targeted to a complementary binding peptide. AsCy3 has good photostability, low pH sensitivity, high absorbance, and good quantum yield. This new probe provides a FRET partner to biarsenical dye FlAsH, making this discovery an important step toward a whole toolkit of colored probes directed to different small peptide motifs.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Cao, H., et al.: J. Am. Chem. Soc., 129, 8672 (2007)<br></p>

<p>Applications The major glucuronide metabolite of Chloramphenicol (C325030).<br>References Simons, P., et al.: Xenobiotica, 22, 1267 (1992), Kaji, H., et al.: Drug Metab. Dispos., 33, 60 (2005),<br></p>

<p>Applications Linagliptin is a novel potent and selective dipeptidyl peptidase-4 (DPP-4) inhibitor with potential use in the treatment of type 2 diabetes.<br>References Prabavathy, N. et al.: Int. J. Pharm. Bio. Sci., 2, 438 (2011); Deacon, C.F.: Diab. Obes. Metab., 13, 7 (2011);<br></p>

<p>Impurity Cefotaxime Sodium EP Impurity E<br>Applications 3-Desacetyl Cefotaxime Lactone is an impurity of Cefotaxime sodium (C242950). 3-Desacetyl Cefotaxime Lactone is also a degradation product for other cephalosporin antibiotics such as: Ceftriaxone (C245000), Cefodizime and Ceftiofur (C244700).<br>References Amaker, R., et al.: Antimicrob. Agents Chemother., 40, 1139 (1996), Taylor, P., et al.: Clin. Biochem., 38, 328 (2005),<br></p>