K-002
Ketamine hydrochloride solution
1.0 mg/mL in methanol (as free base), ampule of 1 mL, certified reference material, Cerilliant®
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About This Item
Produits recommandés
Qualité
certified reference material
Niveau de qualité
Forme
liquid
Caractéristiques
Snap-N-Spike®/Snap-N-Shoot®
Conditionnement
ampule of 1 mL
Fabricant/nom de marque
Cerilliant®
drug control
psicótropo (Spain)
Concentration
1.0 mg/mL in methanol (as free base)
Technique(s)
gas chromatography (GC): suitable
liquid chromatography (LC): suitable
Application(s)
forensics and toxicology
Format
single component solution
Température de stockage
−20°C
InChI
1S/C13H16ClNO.ClH/c1-15-13(9-5-4-8-12(13)16)10-6-2-3-7-11(10)14;/h2-3,6-7,15H,4-5,8-9H2,1H3;1H
Clé InChI
VCMGMSHEPQENPE-UHFFFAOYSA-N
Informations sur le gène
human ... GRIN1(2902) , GRIN2A(2903) , GRIN2B(2904) , GRIN2C(2905) , GRIN2D(2906) , GRIN3A(116443) , GRIN3B(116444)
Catégories apparentées
Description générale
This certified solution standard is suitable for use as starting material in calibrators or controls for a variety of LC/MS or GC/MS testing applications from forensic analysis and clinical toxicology to urine drug testing.
Ketamine is a phencyclidine type of anaesthetic drug that blocks the N-methyl-d-aspartate (NMDA) receptors present on neurons. It is also an abused drug owing to its euphoric and hallucinogenic effects. The drug is also abused at clubs, raves, or parties for its noted hallucinogenic and dissociative properties and is prescribed by some doctors as an off-label treatment for depression.
Ketamine is a phencyclidine type of anaesthetic drug that blocks the N-methyl-d-aspartate (NMDA) receptors present on neurons. It is also an abused drug owing to its euphoric and hallucinogenic effects. The drug is also abused at clubs, raves, or parties for its noted hallucinogenic and dissociative properties and is prescribed by some doctors as an off-label treatment for depression.
Application
The certified reference solution (CRM) in solution can also be used as follows:
- Development of a chiral liquid chromatography-tandem mass spectrometric (LC-MS/MS) method to quantify enantiomers of ketamine and norketamine in plasma, brain, and cerebrospinal fluid samples obtained from mouse
- Multi-residue and non-destructive analysis of ketamine, methamphetamine, heroin, and cocaine by a near-infrared spectroscopic (NIR) method in seized drug samples
- Combined detection and estimation of ketamine, free methamphetamine, pethidine, and tramadol in human urine samples using dispersive liquid-liquid microextraction (DLLME) and gas chromatography-mass spectrometry (GC-MS)
- Electrochemical determination of ketamine in human urine samples using a metal-organic framework/graphene nanocomposite (MOFs@G) modified screen-printed electrode (SPE) after the UV polymerization of molecularly imprinted membranes on its surface
- Simultaneous analysis of ketamine, GHB, norketamine, phenobarbital, thiopental, zolpidem, zopiclone, and phenytoin in human urine samples by a LC-MS/MS procedure following a four-step liquid-liquid extraction of the samples
Caractéristiques et avantages
- Fully characterized under ISO/IEC 17025 and ISO 17034 accreditation
- Accompanied with a comprehensive Certificate of Analysis (CoA) with data on stability, homogeneity, accuracy of concentration, uncertainty, and traceability
- Rigorously tested through real-time stability studies to ensure accuracy and shelf life
- Gravimetrically prepared using qualified precision balances to ensure minimal uncertainty
- Flame sealed under argon into ampoules for long-term shelf life
- Offered in a convenient, DEA-exempt format to improve laboratory efficiency
Informations légales
CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany
Produit(s) apparenté(s)
Réf. du produit
Description
Tarif
Mention d'avertissement
Danger
Mentions de danger
Conseils de prudence
Classification des risques
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1
Organes cibles
Eyes
Code de la classe de stockage
3 - Flammable liquids
Classe de danger pour l'eau (WGK)
WGK 2
Point d'éclair (°F)
49.5 °F - closed cup
Point d'éclair (°C)
9.7 °C - closed cup
Certificats d'analyse (COA)
Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".
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Les clients ont également consulté
Kaixin Fu et al.
Biosensors & bioelectronics, 143, 111636-111636 (2019-09-03)
Ketamine is one of the most widely abused drugs in the world and poses a serious threat to human health and social stability; therefore, the ability to accurately monitor the substance in real-time is necessary. However, several problems still exists
Peter Sos et al.
Neuro endocrinology letters, 34(4), 287-293 (2013-06-28)
Ketamine and other NMDA (N-methyl-D-aspartate) antagonists produce fast-acting antidepressant-like effects, although the underlying mechanism is unclear. Furthermore, high affinity NMDA antagonists such as ketamine are associated with psychotomimetic effects. To date the link between the antidepressant and psychotomimetic effects of
Ketamine-medetomidine regimen for chemical immobilisation of free-ranging chimpanzees (Pan troglodytes schweinfurthii) in Uganda.
D Hyeroba et al.
The Veterinary record, 172(18), 475-475 (2013-04-02)
Waikwong Tang et al.
Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan, 33(2), 164-169 (2013-06-26)
To explore the distribution of TCM patterns in ketamine users and the inter-rater reliability of TCM diagnosis among TCM practitioners. Eighty-four subjects recruited from substance abuse clinics and non-governmental counseling services catering for ketamine abusers were examined by one or
Aude Castel et al.
BMC veterinary research, 9, 59-59 (2013-03-30)
Central post-stroke pain is a neuropathic pain condition caused by a vascular lesion, of either ischemic or hemorrhagic origin, in the central nervous system and more precisely involving the spinothalamocortical pathway responsible for the transmission of painful sensations. Few animal
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