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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC34558 | Tebufenpyrad |
Tebufenpyrad is an acaricide and insecticide widely used in greenhouses. It is commonly used to control populations of mites and ticks.
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| DC36667 | Decane-1 |
Decane-1,10-dithiol is an important raw material and intermediate used in organic synthesis, pharmaceuticals and agrochemicals.
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| DC37532 | Pyridafenthion |
Pyridafenthion is an Agricultural Chemical.
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| DC36961 | Buformin hydrochloride |
Buformin (1-butylbiguanide) is an oral antidiabetic drug of the biguanide class, chemically related to metformin and phenformin. Buformin was marketed by German pharmaceutical company Grünenthal as Silubin. Buformin delays absorption of glucose from the gastrointestinal tract, increases insulin sensitivity and glucose uptake into cells, and inhibits synthesis of glucose by the liver. Buformin and the other biguanides are not hypoglycemic, but rather antihyperglycemic agents. They do not produce hypoglycemia; instead, they reduce basal and postprandial hyperglycemia in diabetics.[5] Biguanides may antagonize the action of glucagon, thus reducing fasting glucose levels.
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| DC37847 | Homocitrulline |
Homocitrulline is an analogue of L-Citrulline, and is an amino acid that occurs in milk products.
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| DC35614 | 4-bromobutylphosphonic acid |
4-bromobutylphosphonic acid is a non-PEG crosslinker
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| DC35488 | PEG15 |
PEG15 is a PEG Linker.
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| DC37835 | Antiflammin P2 |
Antiflammin P2 is a nonapeptide fragment of lipocortin I. Antiflammin P2 has no phospholipase A2 inhibitory & anti-inflammatory activity.
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| DC37735 | L-Acetylleucine |
L-Acetylleucine is used for treating vestibular-related imbalance and vertigo.
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| DC37659 | Hexachlorobenzene |
Hexachlorobenzene is an agricultural fungicide and seed treatment agent.
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| DC35424 | Hydroxy-PEG12-t-butyl ester |
Hydroxy-PEG12-t-butyl ester is a PEG derivative containing a hydroxyl group with a t-butyl ester. The hydrophilic PEG spacer increases solubility in aqueous media. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The t-butyl protected carboxyl group can be deprotected under acidic conditions.
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| DC36063 | APP-CHMINACA |
APP-CHMINACA is a synthetic cannabinoid (CB) featuring a 1-(cyclohexylmethyl)-1H-indazole-3-carboxamide (CHMINACA) base. It displays a 10-fold greater affinity for the central CB1 receptor than that of JWH 018.
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| DC36861 | Homosalate |
Homosalate is an ultraviolet (UV) filtering agent used in sunscreens and other cosmetics for skin protection purposes.
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| DC37090 | Phenyl salicylate |
Phenyl salicylate, or salol, is a chemical substance, introduced in 1886 by Marceli Nencki of Basel. It is synthesized by heating salicylic acid with phenol.
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| DC37535 | Ferric ammonium citrate |
Ferric ammonium citrate is a biochemical.
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| DC37336 | 1-Naphthalenamine |
1-Naphthalenamine, N-ethyl- is a biochemical.
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| DC37043 | Tyrphostin 47 |
Tyrphostin 47 inhibits protein-tyrosine kinase activity of EGF-R both in vitro and in living cells.
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| DC37891 | Lysobactin |
Lysobactin, also known as katanosin B, is a potent antibiotic with in vivo efficacy against Staphylococcus aureus and Streptococcus pneumoniae. It was previously shown to inhibit peptidoglycan (PG) biosynthesis.
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| DC34645 | Toresten |
Thiethylperazine Maleate is a dopamine antagonist which blocks postsynaptic dopamine 2 (D2) receptors.
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| DC37278 | Di-n-octyl phthalate |
Di-n-octyl phthalate is a plasticizer.
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| DC34326 | DEHP |
DEHP is an inducer of cell proliferation in lymphocytes.
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| DC34128 | Dexamethasone acetate |
Dexamethasone acetate is an anti-inflammatory glucocorticoid. Injectable and topical formulations containing dexamethasone acetate have been used to treat inflammation associated with carpal tunnel syndrome, ocular keratitis, asthma exacerbations, and infertility in men.
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| DC35413 | Hydroxy-PEG14-acid |
Hydroxy-PEG14-acid is a PEG derivative containing a hydroxyl group with a terminal carboxylic acid. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond. The hydrophilic PEG spacer increases solubility in aqueous media. The hydroxyl group enables further derivatization or replacement with other reactive functional groups.
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| DC34552 | MMP-9 inhibitor I |
MMP9-IN-I is a cell-permeable, potent, and reversible MMP-9 inhibitor.
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| DC34464 | SKI-II Hydrochloride |
SKI-II HCl is a substrate competitive, reversible, and highly specific inhibitor of sphingosine kinase.
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| DC34273 | CKI-7 dihydrochloride |
CKI-7 2HCl is a casein kinase 1 (CK1) inhibitor.
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| DC36857 | MM 47755 |
MM 47755 is a new benz[a]anthracene antibiotic from a streptomycete.
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| DC38081 | Paclitaxel-Succinic acid |
Paclitaxel-Succinic acid, also known as Paclitaxel Succinate or Paclitaxel-hemisuccinic acid, is a paclitaxel derivative with a succinic acid linker. The carboxy group of Paclitaxel-Succinic acid, after activiating, can be used to conjugate with other molecules such as peptides, proteins, antibodies or enzymes, or polymers. Paclitaxel-Succinic acid is a useful agent to make Paclitaxel-conjugate for drug delivery, nanodrug research.
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| DC35623 | 1,7-Bis-Boc-1,4,7-Triazaheptane |
1,7-Bis-Boc-1,4,7-Triazaheptane is a non-PEG crosslinker.
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| DC33992 | Aminolink phosphoramidite |
Aminolink phosphoramidite for oligonucleotide synthesis. DMS(O)MT is a special protective group similar to traditional MMT, but designed as an improved alternative to it. DMS(O)MT aminolink is fully compatible with standard coupling, deblock, and purification protocols. However, DMS(O)MT group is much better suited for DMT-on and cartridge purification of amino-oligonucleotides because of higher stability, and better oligonucleotide recovery. Oligonucleotides containing DMS(O)MT are more stable in solution than MMT analogs.
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