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cis-(+)-Limonene oxide - 90%, high purity , CAS No.4680-24-4

COA

Grade & Purity:

≥90%

Cas Number: 4680-24-4
Molecular Weight: 152.23
MDL number: MFCD09996820
PubChem CID: 6857487

In stock

Item Number

C487105

Grouped product items
SKU	Size	Availability	Price
C487105-100mg	100mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$113.90
C487105-250mg	250mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$224.90
C487105-1g	1g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$446.90
C487105-5g	5g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$890.90
C487105-25g	25g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$1,778.90

Basic Description

Synonyms	A921062 \| cis-(+)-Limonene oxide \| (+)-(1R,2S,4R)-LIMONENE 1,2-EPOXIDE \| D-LIMONENE 1,2-EPOXIDE \| EMD-15,700 \| N-((1,1-Dimethylpropoxy)carbonyl)-L-tryptophyl-L-methionyl-L-alpha-aspartyl-L-phenylalaninamide \| DB02924 \| +(-)-limonene oxide \| (1R,4R,6S)-1-m
Specifications & Purity	≥90%
Product Description	cis-(+)-Limonene oxide is a valuable chiral terpene oxide building block. Product Application: cis-(+)-Limonene oxide can be used as: A monomer to prepare poly(limonene)carbonate by Al(III) catalyzed coupling reaction with CO2. A reactant to prepare trans-diaxial diol via diastereoselective ring-opening reaction using molybdenum complex catalyst. A reactant to synthesize trans-dihydrocarvone via isomerization reaction in the presence of silica-supported tungstophosphoric acid as a catalyst and dialkylcarbonate as a green solvent

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Oxepanes

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Oxepanes
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Oxepanes
Alternative Parents	Oxacyclic compounds Epoxides Dialkyl ethers Hydrocarbon derivatives
Molecular Framework	Aliphatic heteropolycyclic compounds
Substituents	Oxepane - Oxacycle - Ether - Oxirane - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aliphatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as oxepanes. These are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms.
External Descriptors	(4R)-limonene 1,2-epoxide
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

IUPAC Name	(1R,4R,6S)-1-methyl-4-prop-1-en-2-yl-7-oxabicyclo[4.1.0]heptane
INCHI	InChI=1S/C10H16O/c1-7(2)8-4-5-10(3)9(6-8)11-10/h8-9H,1,4-6H2,2-3H3/t8-,9+,10-/m1/s1
InChIKey	CCEFMUBVSUDRLG-KXUCPTDWSA-N
Smiles	CC(=C)C1CCC2(C(C1)O2)C
Isomeric SMILES	CC(=C)[C@@H]1CC[C@@]2([C@H](C1)O2)C
Molecular Weight	152.23
Reaxy-Rn	111814
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=111814&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Chemical and Physical Properties

Flash Point(°F)	160.7 °F
Flash Point(°C)	71.5 °C
Molecular Weight	152.230 g/mol
XLogP3	2.500
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	1
Exact Mass	152.12 Da
Monoisotopic Mass	152.12 Da
Topological Polar Surface Area	12.500 Å²
Heavy Atom Count	11
Formal Charge	0
Complexity	197.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	3
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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