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C6395

Supelco

Cannabidiol solution

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

Synonym(s):

CBD

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About This Item

Empirical Formula (Hill Notation):
C21H30O2
CAS Number:
13956-29-1
Molecular Weight:
314.46
EC Number:
200-659-6
MDL number:
MFCD00869597
UNSPSC Code:
41116107
PubChem Substance ID:
329775124
NACRES:
NA.24

grade

analytical standard

Quality Level

200

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

SMILES string

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

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

InChI key

QHMBSVQNZZTUGM-ZWKOTPCHSA-N

Gene Information

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

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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).

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.

Signal Word

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

49.5 °F - closed cup

Flash Point(C)

9.7 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000320402
SLCR0734
SLCP0160
SLCH1429
SLCC9048

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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)
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
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)
R G Pertwee
British journal of pharmacology, 153(2), 199-215 (2007-09-11)
Cannabis sativa is the source of a unique set of compounds known collectively as plant cannabinoids or phytocannabinoids. This review focuses on the manner with which three of these compounds, (-)-trans-delta9-tetrahydrocannabinol (delta9-THC), (-)-cannabidiol (CBD) and (-)-trans-delta9-tetrahydrocannabivarin (delta9-THCV), interact with cannabinoid
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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