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(1S)-(-)-alpha-Pinene

Name: (1S)-(-)-alpha-Pinene
Brand: 2A Biotech
SKU: 2A-9034101

CAS Number7785-26-4

Synonyms(1S,5S)-2,6,6-Trimethyl-bicyclo[3.1.1]hept-2-ene; (1S,5S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene; (1S,5S)-Pin-2-ene; MFCD00064145; (1S)-(-)-alpha-Pinene; (1S)-(-)-α-Pinene; α-Pinene; EINECS 232-077-3; L46 A EUTJ A1 A1 D1 &&(-)-α or (1S,5S)- Form; (-)-alpha-pinene; Pinene; (1S,5S)-α-Pinene; (1S,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-ene

Molecular FormulaC10H16

Molecular Weight136.23

Purity98.00%

Density0.9±0.1 g/cm3

Boiling Point157.9±7.0 °C at 760 mmHg

Melting Point-64ºC

AppearanceTransparent and free of impurities

MSDSChinese English

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Cat. No.: 2A-9034101 Purity: 98.00%

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Quality Control of [ 7785-26-4 ] Purity: 98.00% SDS Specification MoL

Chemical & Physical Properties
CAS Number	7785-26-4
Catalog No.	2A-9034101
Chinese Name	(1S)-(-)-α-蒎烯
Synonyms	(1S,5S)-2,6,6-Trimethyl-bicyclo[3.1.1]hept-2-ene; (1S,5S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene; (1S,5S)-Pin-2-ene; MFCD00064145; (1S)-(-)-alpha-Pinene; (1S)-(-)-α-Pinene; α-Pinene; EINECS 232-077-3; L46 A EUTJ A1 A1 D1 &&(-)-α or (1S,5S)- Form; (-)-alpha-pinene; Pinene; (1S,5S)-α-Pinene; (1S,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-ene
Molecular Formula	C10H16
Molecular Weight	136.23
Purity	98.00
Density	0.9±0.1 g/cm3
Boiling Point	157.9±7.0 °C at 760 mmHg
Melting Point	-64ºC
Appearance	Transparent and free of impurities
Water Solubility	Water solubility: insoluble; soluble in: ethanol,
Storage Condition	2-8℃
Packaging	III
Application	(-)-α-Pinene is a monoterpenoid that exhibits sleep-enhancing properties by binding directly to GABAA-benzodiazepine (BZD) receptors as a partial modulator at the BZD binding site.
HTC	29021910
PubChem ID	329768981
SMILES	CC1=CCC2CC1C2(C)C
InChI	InChI=1S/C10H16/c1-7-4-5-8-6-9(7)10(8,2)3/h4,8-9H,5-6H2,1-3H3/t8-,9-/m0/s1
InChI Key	GRWFGVWFFZKLTI-IUCAKERBSA-N
Hazard Symbols	3.0
Bioactivity	(-)-α-Pinene is a monoterpene and shows sleep enhancing property through a direct binding to GABAA-benzodiazepine (BZD) receptors by acting as a partial modulator at the BZD binding site[1]. Related Catalog Signaling Pathways >> Membrane Transporter/Ion Channel >> GABA Receptor Research Areas >> Neurological Disease Signaling Pathways >> Neuronal Signaling >> GABA Receptor In Vitro (-)-α-pinene enhances the quantity of non-rapid eye movement sleep (NREMS) without affecting the intensity of NREMS by prolonging GABAergic synaptic transmission, acting as a partial modulator of GABAA-BZD receptors and directly binding to the BZD binding site of GABAA receptor[1]. References [1]. Yang H, et al. α-Pinene, a Major Constituent of Pine Tree Oils, Enhances Non-Rapid Eye Movement Sleep in Micethrough GABAA-benzodiazepine Receptors. Chemical & Physical Properties Density 0.9±0.1 g/cm3 Boiling Point 157.9±7.0 °C at 760 mmHg Melting Point -64ºC Molecular Formula C10H16 Molecular Weight 136.234 Flash Point 32.2±0.0 °C Exact Mass 136.125198 LogP 4.37 Vapour Pressure 3.5±0.1 mmHg at 25°C Index of Refraction 1.479 InChIKey GRWFGVWFFZKLTI-IUCAKERBSA-N SMILES CC1=CCC2CC1C2(C)C Storage condition 2~8°C
Use of	(-)-α-Pinene is a monoterpene and shows sleep enhancing property through a direct binding to GABAA-benzodiazepine (BZD) receptors by acting as a partial modulator at the BZD binding site[1]. Properties Name (-)-α-pinene Synonym More Synonyms (1S)-(-)-Alpha-Pinene Biological Activity Description (-)-α-Pinene is a monoterpene and shows sleep enhancing property through a direct binding to GABAA-benzodiazepine (BZD) receptors by acting as a partial modulator at the BZD binding site[1]. Related Catalog Signaling Pathways >> Membrane Transporter/Ion Channel >> GABA Receptor Research Areas >> Neurological Disease Signaling Pathways >> Neuronal Signaling >> GABA Receptor In Vitro (-)-α-pinene enhances the quantity of non-rapid eye movement sleep (NREMS) without affecting the intensity of NREMS by prolonging GABAergic synaptic transmission, acting as a partial modulator of GABAA-BZD receptors and directly binding to the BZD binding site of GABAA receptor[1]. References [1]. Yang H, et al. α-Pinene, a Major Constituent of Pine Tree Oils, Enhances Non-Rapid Eye Movement Sleep in Micethrough GABAA-benzodiazepine Receptors. Chemical & Physical Properties Molecular Formula C10H16 Exact Mass 136.125198 Index of Refraction 1.479 InChIKey GRWFGVWFFZKLTI-IUCAKERBSA-N
Tax Rebate	9.0%
Supervision	none
Transport Info	Product name: Purity: 99.0%
MSDS Transport Info	Module 14. Shipping information 14.1 UN number European Dangerous Regulations for land transport: 2368 International Dangerous Regulations for sea transport: 2368 International Dangerous Regulations for air transport: 2368 14.2 Names specified by the United Nations (UN) European Land Transport Danger Regulation: alpha-PINENE IMDG Code: alpha-PINENE International air transport hazard regulations: alpha-Pinene 14.3 Transport hazard categories European land transport Dangerous Regulations: 3 International sea transport Dangerous Regulations: 3 International air transport Dangerous Regulations: 3 14.4 Package group European Land Transport Danger Regulations: III International Maritime Transport Danger Regulations: III International Air Transport Danger Regulations: III 14.5 Environmental hazards European Land Transport Dangerous Regulations: Yes International Maritime Transport Dangerous Regulations Maritime Pollutants: Yes International Air Transport Dangerous Regulations: No 14.6 Special reminder to users No data available

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(1S)-(-)-alpha-Pinene

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