CAS 19902-08-0

beta-pinene

Description:

Beta-pinene is a bicyclic monoterpene with the chemical formula C10H16, characterized by its distinct pine-like aroma. It is a colorless to pale yellow liquid at room temperature and is insoluble in water but soluble in organic solvents. Beta-pinene is primarily found in the essential oils of various plants, particularly conifers, and is commonly used in the fragrance and flavor industries. Its structure features a cyclobutane ring and a double bond, contributing to its reactivity and potential applications in organic synthesis. Beta-pinene exhibits antimicrobial and antifungal properties, making it of interest in natural product chemistry and potential therapeutic applications. Additionally, it can undergo polymerization and oxidation reactions, leading to the formation of various derivatives. Due to its pleasant scent, beta-pinene is also utilized in the production of perfumes, cleaning products, and as a flavoring agent in food. Safety data indicates that while it is generally regarded as safe in low concentrations, it should be handled with care due to potential irritant effects.

Formula: C₁₀H₁₆

InChI: InChI=1/C10H16/c1-7-4-5-8-6-9(7)10(8,2)3/h8-9H,1,4-6H2,2-3H3/t8-,9-/m1/s1

SMILES: C=C1CC[C@@H]2C[C@H]1C2(C)C

Synonyms:

• Terbenthene
• 2(10)-Pinene
• 2,2,6-Trimethylbicyclo(3.1.1)Hept-2-Ene
• 6,6-Dimethyl-2-Methylenebicyclo(3.1.1)Heptane
• 6,6-Dimethyl-2-Methylenenorpinane
• Ai3-24483
• Bicyclo(3.1.1)Heptane, 6,6-Dimethyl-2-Methylene-
• Monoterpenes
• Nopinen
• Nopinene
• Pinene, Beta
• Pseudopinen
• Pseudopinene
• Rosemarel
• Terebenthene
• Beta-Pinene (Natural)
• (1)-6,6-Dimethyl-2-Methylenebicyclo(3.1.1)Heptane
• 6,6-Dimethyl-2-Methylene-Bicyclo(3.1.1)Heptane
• Pin-2(10)-Ene
• Pinene
• 6,6-Dimethyl-2-Methylidenebicyclo[3.1.1]Heptane

(1R,5R)-6,6-dimethyl-2-methylidenebicyclo[3.1.1]heptane

CAS: 19902-08-0

Formula: C₁₀H₁₆

Color and Shape: Liquid

Molecular weight: 136.234

Ref: IN-DA002BW9

ASTM Method D7845 Check Standard 0.01-0.05 Wt% in Toluene

Controlled Product

CAS: 100-42-5, 100-80-1, 105-67-9, 108-93-0, 108-95-2, 1195-32-0, 122-99-6, 123-07-9, 141-32-2, 142-96-1, 19902-08-0, 2039-89-6, 2234-20-0, 25837-05-2, 4169-04-4, 5989-27-5, 60-12-8, 611-15-4, 620-17-7, 622-97-9, 71-36-3, 77-73-6, 770-35-4, 80-56-8, 873-66-5, 90-00-6, 90-12-0, 91-20-3, 91-57-6, 93-56-1, 95-13-6, 98-83-9, 98-85-1, 99-89-8

Color and Shape: Mixture

Ref: 04-GS09001085TO

(+)-β-Pinene

CAS: 19902-08-0

Formula: C₁₀H₁₆

Molecular weight: 136.24

Ref: 4Z-P-265005

(+)-β-Pinene

Controlled Product

CAS: 19902-08-0

Formula: C₁₀H₁₆

Color and Shape: Neat

Molecular weight: 136.23

Ref: TR-P466618

R-(+)-β-Pinene-D2,13C

Controlled Product

CAS: 19902-08-0

Formula: CC₉D₂H₁₄

Color and Shape: Neat

Molecular weight: 139.239

Ref: TR-P466619

(1R,5R)-6,6-Dimethyl-2-methylene-bicyclo[3.1.1]Heptane

CAS: 19902-08-0

(1R,5R)-6,6-Dimethyl-2-methylene-bicyclo[3.1.1]Heptane is a deuterated geranyl compound that has been shown to have neuroprotective properties in animal models of Parkinson's disease and Alzheimer's disease. As a phosphite, it reacts with acids to form phosphoric acid and water. The acidic proton on the geranyl group can be protonated by protic solvents such as water and alcohols to form the corresponding alcoholate esters. This compound is biosynthesized from dietary sulfur, which contains sulfur atoms derived from sulfurous compounds such as hydrogen sulfide or cysteine (amino acid). The ligand has been rationalized through its similarity to fructus aurantii immaturus.

Formula: C₁₀H₁₆

Purity: Min. 95%

Molecular weight: 136.23 g/mol

Ref: 3D-FD143194