4-Piperidinylmethyl+isonicotinate+hydrochloride
Catalog Number:
(EM-AX0114-1)
Supplier:
MilliporeSigma
Description:
Acetone ≥99.5% (by GC, corrected for water content) for pesticide residue analysis, Supelco®
Supplier:
ALADDIN SCIENTIFIC
Description:
2-Acetylthiazole is useful for preparing triazolothiazoles, chiral alcohols, and in aldol condensation reactions.Useful for preparation of triazolothiazoles,chiral alcohols,and in aldol condensation reactions.
Catalog Number:
(10430-698)
Supplier:
Bioss
Description:
Acts as an electrogenic sodium (Na(+)) and chloride (Cl-)-dependent sodium-coupled solute transporter, including transport of monocarboxylates (short-chain fatty acids including L-lactate, D-lactate, pyruvate, acetate, propionate, valerate and butyrate), lactate, mocarboxylate drugs (nicotinate, benzoate, salicylate and 5-aminosalicylate) and ketone bodies (beta-D-hydroxybutyrate, acetoacetate and alpha-ketoisocaproate), with a Na(+):substrate stoichiometry of between 4:1 and 2:1. Catalyzes passive carrier mediated diffusion of iodide. Mediates iodide transport from the thyrocyte into the colloid lumen through the apical membrane. May be responsible for the absorption of D-lactate and monocarboxylate drugs from the intestinal tract. Acts as a tumor suppressor, suppressing colony formation in colon cancer, prostate cancer and glioma cell lines. May play a critical role in the entry of L-lactate and ketone bodies into neurons by a process driven by an electrochemical Na(+) gradient and hence contribute to the maintenance of the energy status and function of neurons.
Catalog Number:
(TCO0218-001ML)
Supplier:
TCI America
Description:
CAS Number: 589-63-9
MDL Number: MFCD00027241 Molecular Formula: C8H16O Molecular Weight: 128.22 Purity/Analysis Method: >98.0% (GC) Form: Clear Liquid Boiling point (°C): 166 Specific Gravity (20/20): 0.82
Catalog Number:
(10408-230)
Supplier:
Bioss
Description:
Key enzyme for ketone body catabolism. Transfers the CoA moiety from succinate to acetoacetate. Formation of the enzyme-CoA intermediate proceeds via an unstable anhydride species formed between the carboxylate groups of the enzyme and substrate.
Catalog Number:
(10408-240)
Supplier:
Bioss
Description:
Key enzyme for ketone body catabolism. Transfers the CoA moiety from succinate to acetoacetate. Formation of the enzyme-CoA intermediate proceeds via an unstable anhydride species formed between the carboxylate groups of the enzyme and substrate.
Catalog Number:
(TCD1536-005ML)
Supplier:
TCI America
Description:
CAS Number: 19780-10-0
MDL Number: MFCD00015290 Molecular Formula: C12H24O Molecular Weight: 184.32 Purity/Analysis Method: >97.0% (GC) Form: Clear Liquid Flash Point (°C): 66 Specific Gravity (20/20): 0.83
Catalog Number:
(10346-030)
Supplier:
Bioss
Description:
Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate (By similarity).
Catalog Number:
(10346-024)
Supplier:
Bioss
Description:
Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate (By similarity).
Supplier:
TCI America
Description:
CAS Number: 563-80-4
MDL Number: MFCD00008919 Molecular Formula: C5H10O Molecular Weight: 86.13 Purity/Analysis Method: >99.0% (GC) Form: Clear Liquid Boiling point (°C): 93 Melting point (°C): -92 Flash Point (°C): 1 Specific Gravity (20/20): 0.80
Catalog Number:
(TCM0234-010ML)
Supplier:
TCI America
Description:
CAS Number: 2550-21-2
MDL Number: MFCD00039948 Molecular Formula: C7H14O Molecular Weight: 114.19 Purity/Analysis Method: >98.0% (GC) Form: Clear Liquid Boiling point (°C): 145 Flash Point (°C): 38 Specific Gravity (20/20): 0.82
Supplier:
BTNX INC.
Description:
The Rapid Response® Urinalysis reagent strip is a fast, qualitative and semi-quantitative, dip-and-read test for the detection of urine analytes in human urine, to aid in the general evaluation of health and in the diagnosis and monitoring of metabolic or systemic diseases.
Catalog Number:
(TCA1629-5G)
Supplier:
TCI America
Description:
CAS Number: 2879-20-1
MDL Number: MFCD00006823 Molecular Formula: C10H10O3 Molecular Weight: 178.19 Purity/Analysis Method: >98.0% (GC) Form: Crystal Melting point (°C): 84
Supplier:
AMBEED, INC
Description:
1-(Furan-2-yl)ethanone, Purity: 98%, CAS Number: 1192-62-7, Appearance: Colorless to Yellow Liquid or Semi-Solid or solid, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 100g
Catalog Number:
(10430-696)
Supplier:
Bioss
Description:
Acts as an electrogenic sodium (Na(+)) and chloride (Cl-)-dependent sodium-coupled solute transporter, including transport of monocarboxylates (short-chain fatty acids including L-lactate, D-lactate, pyruvate, acetate, propionate, valerate and butyrate), lactate, mocarboxylate drugs (nicotinate, benzoate, salicylate and 5-aminosalicylate) and ketone bodies (beta-D-hydroxybutyrate, acetoacetate and alpha-ketoisocaproate), with a Na(+):substrate stoichiometry of between 4:1 and 2:1. Catalyzes passive carrier mediated diffusion of iodide. Mediates iodide transport from the thyrocyte into the colloid lumen through the apical membrane. May be responsible for the absorption of D-lactate and monocarboxylate drugs from the intestinal tract. Acts as a tumor suppressor, suppressing colony formation in colon cancer, prostate cancer and glioma cell lines. May play a critical role in the entry of L-lactate and ketone bodies into neurons by a process driven by an electrochemical Na(+) gradient and hence contribute to the maintenance of the energy status and function of neurons.
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