1124-25-0

Basic information

• Product Name: (1α,4β)-p-Menth-8-ene
• Synonyms: (1α,4β)-p-Menth-8-ene;trans-p-Menth-8-ene
• CAS NO: 1124-25-0
• Molecular Formula: C₁₀H₁₈
• Molecular Weight: 138.25
• Mol File: 1124-25-0.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (1α,4β)-p-Menth-8-ene(CAS DataBase Reference)
• NIST Chemistry Reference: (1α,4β)-p-Menth-8-ene(1124-25-0)
• EPA Substance Registry System: (1α,4β)-p-Menth-8-ene(1124-25-0)

Safety Data

• Hazardous Substances Data: 1124-25-0(Hazardous Substances Data)

Usage

General Description

(1α,4β)-p-Menth-8-ene is a chemical compound with a molecular formula of C10H16. It is a bicyclic monoterpene and a member of the menthane class of organic compounds. (1α,4β)-p-Menth-8-ene is found naturally in various essential oils, such as mint, and is commonly used in the fragrance and flavoring industries. It has a characteristic minty, herbal aroma and is often used in products such as perfumes, soaps, and cosmetics. In addition to its olfactory properties, (1α,4β)-p-Menth-8-ene also has potential medicinal benefits, including antimicrobial and anti-inflammatory properties.

Upstream product

• 55816-07-4 citronellyl iodide 
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• 1124-27-2 p-4⁽⁸⁾-menthene 
• 5114-00-1 trans-p-menthan-8-ol 
• 138-86-3 limonene. 
• 5989-27-5 D-limonene 
• 554-59-6 trans-Carane 
• 554-59-6 cis-Carane 
• 1197-01-9 p-cymene-8-ol 
• 94-08-6 4-methylbenzoic acid ethyl ester 
• 98-55-5 terpineol 
• 41144-01-8 (+/-)-citronellyl tosylate 
• 4795-86-2 (1R)-(+)-cis-pinane 

Downstream Products

• 106933-00-0 N-p-menth-8-ylacetamide 

Relevant articles and documents

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Amberlyst-15: A reusable heterogeneous catalyst for the dehydration of tertiary alcohols

Tertiary alcohols react under mild conditions in the presence of Amberlyst-15 (dry) (solid-supported sulfonic acid) to give predominantly the most stable alkene in very good yield. The dehydration of tertiary alcohol functionality occurs without observation of rearrangement and polymerization products, and with outstanding substrate tolerance, which include the NHCBz, NHBoc, OSEM, OTBDMS, OBOM and ethylene ketal functional groups. Amberlyst-15 (dry) can be easily recovered from the reaction medium and reused for five cycles, maintaining the catalytic efficiency. In addition, the dehydration can occur under continuous operation.

SYNTHESIS AND THERMOCHEMICAL PARAMETERS OF 1-p-MENTHENE AND 3-p-MENTHENE

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TRANSFORMATIONS OF cis- AND trans-CARENES IN THE PRESENCE OF ZEOLITE CATALYSTS

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