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Merck

C6395

Cannabidiol solution

1.0 mg/mL in methanol, analytical standard, for drug analysis

Sinónimos:

CBD

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About This Item

Fórmula empírica (notación de Hill):
C21H30O2
Número CAS:
Peso molecular:
314.46
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
EC Number:
200-659-6
MDL number:

Nombre del producto

Cannabidiol solution, 1.0 mg/mL in methanol, analytical standard, for drug analysis

InChI key

QHMBSVQNZZTUGM-ZWKOTPCHSA-N

InChI

1S/C21H30O2/c1-5-6-7-8-16-12-19(22)21(20(23)13-16)18-11-15(4)9-10-17(18)14(2)3/h11-13,17-18,22-23H,2,5-10H2,1,3-4H3/t17-,18+/m0/s1

SMILES string

CCCCCc1cc(O)c([C@@H]2C=C(C)CC[C@H]2C(C)=C)c(O)c1

grade

analytical standard

concentration

1.0 mg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

pharmaceutical (small molecule)

format

single component solution

storage temp.

2-8°C

Quality Level

Gene Information

human ... CNR1(1268), CNR2(1269)
rat ... Cnr1(25248)

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Application

Cannabidiol is used as an analytical reference standard for the quantification of the analyte in hashish drug samples and plasma samples using chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

General description

Cannabidiol belongs to the group of active cannabinoids, available in neutral form, derived from Cannabis species and is available as a main component of illicit drugs such as hashish (cannabis resin) and marijuana (herbal cannabis).

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

target_organs

Eyes,Central nervous system

Clase de almacenamiento

3 - Flammable liquids

wgk

WGK 2

flash_point_f

49.5 °F - closed cup

flash_point_c

9.7 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves


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Simultaneous separation and identification of hashish constituents by coupled liquid chromatography-mass spectrometry (HPLC-MS)
Rustichelli.C, et al.
Chromatographia, 43(3-4), 129-134 (1996)
Development of a simple and sensitive HPLC?UV method for the simultaneous determination of cannabidiol and ?9-tetrahydrocannabinol in rat plasma
Zgair A, et al.
Journal of Pharmaceutical and Biomedical Analysis, 114(3-4), 145-151 (2015)
Maiko Tsuchiya et al.
International journal of molecular sciences, 20(24) (2019-12-15)
Bone metabolism is strictly regulated, and impaired regulation caused by hormonal imbalances induces systemic bone loss. Local bone loss caused by tumor invasion into bone is suggested to be induced by the generation of cytokines, which affect bone metabolism, by
Antonio Waldo Zuardi
Revista brasileira de psiquiatria (Sao Paulo, Brazil : 1999), 30(3), 271-280 (2008-10-04)
The aim of this review is to describe the historical development of research on cannabidiol. This review was carried out on reports drawn from Medline, Web of Science and SciELO. After the elucidation of the chemical structure of cannabidiol in
Alline Cristina Campos et al.
Psychopharmacology, 226(1), 13-24 (2012-09-26)
Cannabidiol (CBD) is a non-psychotomimetic constituent of Cannabis sativa plant that promotes antianxiety and anti-panic effects in animal models after acute systemic or intra-dorsal periaqueductal gray (DPAG) administration. However, the effects of CBD repeated administration, and the possible mechanisms involved

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