524 Results for: "1-Benzylpiperidine-4-carboxylic acid hydrochloride&amp"

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Ciprofloxacin hydrochloride monohydrate 98.0-102.0%

Supplier: Thermo Scientific Chemicals

An anti-bacterial agent effective against anaerobic bacteria

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Methyl trans-4-aminocyclohexanecarboxylate hydrochloride 97%

Supplier: Ambeed

Methyl trans-4-aminocyclohexanecarboxylate hydrochloride 97%

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Moxifloxacin hydrochloride ≥99%

Supplier: Matrix Scientific

Matrix Scientific Part Number: 047902-1G , MDL Number: MFCD00949117

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Moxifloxacin hydrochloride monohydrate ≥98.0% (by HPLC, titration analysis)

Supplier: TCI America

Moxifloxacin Hydrochloride Monohydrate, >98%, 192927-63-2, C21H24FN3O4.HCl.H2O, Synonym: 1-Cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-7-[(4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridin-6-yl]-4-oxo-3-quinolinecarboxylic Acid Hydrochloride Monohydrate, Size: 1G

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Moxifloxacin hydrochloride 97%

Supplier: Thermo Scientific Chemicals

A broad spectrum antibiotic commonly used against bacteria which cause sinus and lung infections

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Lomefloxacin hydrochloride ≥98.0% (by HPLC, titration analysis)

Supplier: TCI America

CAS Number: 98079-52-8
MDL Number: MFCD00214312
Molecular Formula: C17H19F2N3O3
Molecular Weight: 387.81
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal

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Ciprofloxacin hydrochloride monohydrate ≥98.0% (by HPLC, titration analysis)

Supplier: TCI America

CAS Number: 86393-32-0
MDL Number: MFCD00242856
Molecular Formula: C17H18FN3O3
Molecular Weight: 367.81
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal

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Methyl trans-4-aminocyclohexanecarboxylate hydrochloride ≥98.0% (by total nitrogen and titration analysis)

Supplier: TCI America

CAS Number: 61367-07-5
MDL Number: MFCD08274538
Molecular Formula: C8H15NO2
Molecular Weight: 193.67
Purity/Analysis Method: >98.0% (N,T)
Form: Crystal

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Vancomycin hydrochloride (from Streptomyces lysosup)

Supplier: Enzo Life Sciences

Glycopeptide antibiotic

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Vancomycin hydrochloride ≥900 µg/mg

Supplier: Ambeed

Vancomycin hydrochloride ≥900 µg/mg

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TRC 3’-Amino-2’-Hydroxy-[1,1’]biphenyl-3-carboxylic Acid

Supplier: LGC Standards

TRC 3’-Amino-2’-Hydroxy-[1,1’]biphenyl-3-carboxylic Acid

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Vancomycin hydrochloride >900 µg/mg

Supplier: Thermo Scientific Chemicals

Vancomycin hydrochloride >900 µg/mg

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1-Aminocyclobutanecarboxylic acid ≥97%

Supplier: Matrix Scientific

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Ciprofloxacin hydrochloride monohydrate

Supplier: MP Biomedicals

Ciprofloxacin is a fluorinated quinolone antibacterial agent which is highly effective against a broad spectrum of bacteria and mycoplasma.
Ciprofloxacin is most commonly used to treat infections of the skin, bone, sinus, lung, abdomen, and bladder. It can also be used to treat some sexually transmitted infections. Additionally, ciprofloxacin can be used after exposure to inhalation anthrax to reduce the chance of developing an infection.
During the proliferation phase of a bacterium a segmental twisting and untwisting of the chromosomes take place. An enzyme called DNA gyrase plays a decisive part in this process. Ciprofloxacin inhibits this DNA gyrase in a way that arrests the bacterial metabolism, since vital information can no longer be read from the bacterial chromosome. Ultimately, it affect DNA replication & cell division.
Store at +4 °C.

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Vancomycin hydrochloride for molecular biology

Supplier: Thermo Scientific Chemicals

Inhibits bacterial mucopeptide synthesis.

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Vancomycin hydrochloride 50 mg/ml in distilled water, sterile filtered

Supplier: Thermo Scientific Chemicals

Vancomycin hydrochloride, 50 mg/mL in distilled water, sterile-filtered.

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TRC 4-Amino-2-methyl-10H-thieno[2,3-b][1,5]-benzodiazapine, Hydrochloride

Supplier: LGC Standards

TRC 4-Amino-2-methyl-10H-thieno[2,3-b][1,5]-benzodiazapine, Hydrochloride

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Vancomycin hydrochloride (from Streptomyces orientalis), powder

Supplier: MP Biomedicals

Vancomycin inhibits bacterial mucopeptide biosynthesis

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EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Pierce™

Supplier: Invitrogen

Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.