(S)-(−)-Perillyl alcohol - ≥96% , CAS No.18457-55-1

CAS: 18457-55-1 Cat. No.: S468317 Peso molecular: 152.23 Número EC: 629-611-6 PubChem CID: 369312
Disponible para pedir
GRADE & PURITY ≥96%
Synonyms
(-)-Perillyl alcohol | Perycorolle | (3-METHYL-2-OXO-2,3-DIHYDRO-1H-BENZIMIDAZOL-1-YL)ACETICACID | (4S)-perillyl alcohol | (S)-(?)-Perillyl alcohol | NSC-641066 | UNII-3UL4QIY642 | (S)-(4-(prop-1-en-2-yl)cyclohex-1-enyl)methanol | F16807 | MFCD00062995 |
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
250mg
S468317-250mg
2

10,90US$

16,90US$
Guardar 6,00 US$ (35.50%)
1g
S468317-1g
2

25,90US$

38,90US$
Guardar 13,00 US$ (33.42%)
5g
S468317-5g
1

77,90US$

116,90US$
Guardar 39,00 US$ (33.36%)
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Why this grade

≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

(S)-(-)-Perillyl alcohol is a monoterpenoid compound found in the essential oils of cherries, lavender and spearmint. It shows potent anticancer activity.(S)-(−)-Perillyl alcohol (POH or 4-isopropenyl cyclohexene carbinol) can be used as a starting material in the synthesis of:Perillyl alcohol neoglycoside derivatives as potential anti cancer agents.Amino-modified derivatives of (S)-perillyl alcohol as potent antiproliferative agents.Perillaldehyde 8,9-epoxide, apara-menthane class derivative as anin vivoanti-tumor agent.

Specifications

Sinónimos
(-)-Perillyl alcohol | Perycorolle | (3-METHYL-2-OXO-2, 3-DIHYDRO-1H-BENZIMIDAZOL-1-YL)ACETICACID | (4S)-perillyl alcohol | (S)-(?)-Perillyl alcohol | NSC-641066 | UNII-3UL4QIY642 | (S)-(4-(prop-1-en-2-yl)cyclohex-1-enyl)methanol | F16807 | MFCD00062995 |
Especificaciones y pureza
≥96%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥96%
Nombres e identificadores
Pubchem Sid504758598
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504758598
Sonrisas canónicasCC(=C)C1CCC(=CC1)CO
IUPAC Name[(4S)-4-prop-1-en-2-ylcyclohexen-1-yl]methanol
InChIKeyNDTYTMIUWGWIMO-SNVBAGLBSA-N
INCHI1S/C10H16O/c1-8(2)10-5-3-9(7-11)4-6-10/h3,10-11H,1,4-7H2,2H3/t10-/m1/s1
Isómeros SMILES CC(=C)[C@H]1CCC(=CC1)CO
PubChem CID 369312
Peso molecular 152.23

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClasePrenol lipids
SubclassMonoterpenoids
Intermediate Tree Nodes Not available
Direct ParentMenthane monoterpenoids
Alternative Parents Monocyclic monoterpenoids  Primary alcohols  Hydrocarbon derivatives  
Molecular FrameworkAliphatic homomonocyclic compounds
Substituents P-menthane monoterpenoid - Monocyclic monoterpenoid - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic homomonocyclic compound
DescripciónThis 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 Menthane monoterpenoids
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
PLK1 Tchem Serine/threonine-protein kinase PLK1 (28605 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A498 (42825 Activities)
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ACHN (49357 Activities)
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CAKI-1 (44928 Activities)
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CCRF-CEM (65223 Activities)
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COLO 205 (50209 Activities)
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DLD-1 (17511 Activities)
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DU-145 (51482 Activities)
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HL-60 (67320 Activities)
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HT-29 (80576 Activities)
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K562 (73714 Activities)
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KM12 (47707 Activities)
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M14 (47487 Activities)
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MCF7 (126967 Activities)
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MOLT-4 (49676 Activities)
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OVCAR-3 (48710 Activities)
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OVCAR-4 (44535 Activities)
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OVCAR-5 (45555 Activities)
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OVCAR-8 (47708 Activities)
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PC-3 (62116 Activities)
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RPMI-8226 (44974 Activities)
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RXF 393 (41971 Activities)
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RXF 631 (11415 Activities)
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SF-295 (48000 Activities)
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SK-MEL-2 (46422 Activities)
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SK-MEL-28 (48833 Activities)
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SK-MEL-5 (47095 Activities)
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SK-OV-3 (52876 Activities)
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SN12C (47755 Activities)
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SNB-19 (46794 Activities)
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SNB-78 (14240 Activities)
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TK-10 (45540 Activities)
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U-251 (51189 Activities)
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UACC-257 (46019 Activities)
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UACC-62 (47335 Activities)
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UO-31 (46270 Activities)
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XF498 (12972 Activities)
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786-0 (47912 Activities)
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A549 (127892 Activities)
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NCI/ADR-RES (33767 Activities)
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T47D (39041 Activities)
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EKVX (44102 Activities)
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NCI-H322M (45589 Activities)
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HCC 2998 (41480 Activities)
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HCT-116 (91556 Activities)
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HOP-92 (41141 Activities)
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Hs-578T (29457 Activities)
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NCI-H460 (60772 Activities)
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SF-268 (49410 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
IGROV-1 (47897 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
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Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot NumberCertificate TypeFechaArticulo
J2323239Certificate of AnalysisOct 08, 2023 S468317
J2325236Certificate of AnalysisOct 08, 2023 S468317
J2325237Certificate of AnalysisOct 08, 2023 S468317
J2325238Certificate of AnalysisOct 08, 2023 S468317
J2325239Certificate of AnalysisOct 08, 2023 S468317
J2325240Certificate of AnalysisOct 08, 2023 S468317
J2325241Certificate of AnalysisOct 08, 2023 S468317
Propiedades químicas y físicas
Índice de refracciónn20/D 1.501
Rotación específica [α][α]22/D −88°, c = 1 in methanol
Punto de ebullición (°C)119-121 °C/11 mmHg
Peso molecular152.230 g/mol
XLogP32.100
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count2
Exact Mass152.12 Da
Monoisotopic Mass152.12 Da
Topological Polar Surface Area20.200 Ų
Heavy Atom Count11
Formal Charge0
Complexity179.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Feng Gao, Zhongkun Zhang, Minzi Ju, Liang Bian, Huijuan Wang, Sibo Zhao, Ningbo Cai, Yu Wang, Yanpeng Jia, Ling Shen, Yuan Zhang, Honghong Yao.  (2025)  Therapeutic Delivery of circDYM by Perillyl Alcohol Nanoemulsion Alleviates LPS-Induced Depressive-Like Behaviors.  Advanced Science,      [PMID:40145792] [10.1002/advs.202414559]
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