SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

📚

Preuve documentaire

Cité dans 37 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Spécifications

Synonymes

Spécifications et pureté

≥95%

Conditions de stockage de stockage

Store at 2-8°C

Expédié en

Wet ice

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Pureté

≥95%

Noms et identifiants

Pubchem Sid

508810441

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508810441

Sourires canoniques

CC1=CCC(CC1)C(=C)C

IUPAC Name

1-methyl-4-prop-1-en-2-ylcyclohexene

InChIKey

XMGQYMWWDOXHJM-UHFFFAOYSA-N

INCHI

1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,10H,1,5-7H2,2-3H3

Isomères SMILES

CC1=CCC(CC1)C(=C)C

Poids moléculaire

136.234

Reaxy-Rn

774123

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=774123&ln=

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.

Rechercher le COA →

📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

Voir la fiche technique →

🔬 Fiche de spécifications

Attributs de qualité complets et critères d'acceptation pour cette qualité.

Voir la fiche de spécifications →

Données avancées

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Classe Prenol lipids
    - Subclass Monoterpenoids

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Classe	Prenol lipids
Subclass	Monoterpenoids
Intermediate Tree Nodes	Not available
Direct Parent	Menthane monoterpenoids
Alternative Parents	Monocyclic monoterpenoids Branched unsaturated hydrocarbons Cycloalkenes Unsaturated aliphatic hydrocarbons
Molecular Framework	Aliphatic homomonocyclic compounds
Substituents	P-menthane monoterpenoid - Monocyclic monoterpenoid - Branched unsaturated hydrocarbon - Cycloalkene - Cyclic olefin - Unsaturated aliphatic hydrocarbon - Unsaturated hydrocarbon - Olefin - Hydrocarbon - Aliphatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.
External Descriptors	a limonene
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

Structure 3D

Cibles associées (humaines)

THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)

Discover Target: THRB

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RXRA Tclin Retinoid X receptor alpha (3637 Activities)

Discover Target: RXRA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TP53 Tchem Cellular tumor antigen p53 (48468 Activities)

Discover Target: TP53

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

A498 (42825 Activities)

Lot Number	Certificate Type	Date	Article
H2611334	Certificate of Analysis	Jul 18, 2026	D304599
H2611182	Certificate of Analysis	Jul 18, 2026	D304599
G2618161	Certificate of Analysis	Apr 10, 2026	D304599
D2622223	Certificate of Analysis	Apr 10, 2026	D304599
D2622224	Certificate of Analysis	Apr 10, 2026	D304599
D2622258	Certificate of Analysis	Apr 10, 2026	D304599
F23151071	Certificate of Analysis	Mar 18, 2026	D304599
F23151034	Certificate of Analysis	Mar 18, 2026	D304599
J2511359	Certificate of Analysis	Sep 19, 2025	D304599
J2511358	Certificate of Analysis	Sep 19, 2025	D304599
J2511357	Certificate of Analysis	Sep 19, 2025	D304599
G2529163	Certificate of Analysis	Jul 11, 2025	D304599
G2529266	Certificate of Analysis	Jul 11, 2025	D304599
G2529265	Certificate of Analysis	Jul 11, 2025	D304599
C2605196	Certificate of Analysis	Jul 11, 2025	D304599
C2510120	Certificate of Analysis	Feb 28, 2025	D304599
C2510121	Certificate of Analysis	Feb 28, 2025	D304599
C2510122	Certificate of Analysis	Feb 28, 2025	D304599
H2415353	Certificate of Analysis	Aug 02, 2024	D304599
H2415352	Certificate of Analysis	Aug 02, 2024	D304599
H2415332	Certificate of Analysis	Aug 02, 2024	D304599
C2407426	Certificate of Analysis	Feb 26, 2024	D304599
C2407431	Certificate of Analysis	Feb 26, 2024	D304599
C2407432	Certificate of Analysis	Feb 26, 2024	D304599
B2510007	Certificate of Analysis	Feb 26, 2024	D304599
J2312594	Certificate of Analysis	Sep 23, 2023	D304599
J2312597	Certificate of Analysis	Sep 23, 2023	D304599
J2312599	Certificate of Analysis	Sep 23, 2023	D304599
F23151052	Certificate of Analysis	Jun 02, 2023	D304599
I2306035	Certificate of Analysis	Jun 02, 2023	D304599
F23151038	Certificate of Analysis	Jun 02, 2023	D304599
F23151037	Certificate of Analysis	Jun 02, 2023	D304599
H2224193	Certificate of Analysis	Jul 28, 2022	D304599
H2224194	Certificate of Analysis	Jul 28, 2022	D304599
H2224192	Certificate of Analysis	Jul 28, 2022	D304599
D2307416	Certificate of Analysis	Jul 28, 2022	D304599
E2319194	Certificate of Analysis	Jul 28, 2022	D304599
F2221251	Certificate of Analysis	Nov 19, 2021	D304599

Point d'éclair (°C)	45℃
Point d'ébullition (°C)	176℃
Point de fusion (°C)	-97℃
Poids moléculaire	136.230 g/mol
XLogP3	3.400
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	0
Rotatable Bond Count	1
Exact Mass	136.125 Da
Monoisotopic Mass	136.125 Da
Topological Polar Surface Area	0.000 Å²
Heavy Atom Count	10
Formal Charge	0
Complexity	163.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	1
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

D-Limonene - ≥95% , CAS No.7705-14-8

Stockage & expédition

Documents qualité

Preuve documentaire

Spécifications

Documentation

📋 Fiche de données de sécurité (FDS)

✅ Certificat d'analyse (COA)

📊 Fiche technique

🔬 Fiche de spécifications

Données avancées

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Avis des clients

📚 Citations par application

View related series