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Supelco

(−)-Perillyl alcohol

analytical standard

Synonym(s):

(S)-4-Isopropenyl-1-cyclohexenylmethanol, (S)-p-Mentha-1,8-dien-7-ol

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About This Item

Empirical Formula (Hill Notation):
C10H16O
CAS Number:
18457-55-1
Molecular Weight:
152.23
Beilstein:
2501605
MDL number:
MFCD00062995
UNSPSC Code:
85151701
PubChem Substance ID:
329767604
NACRES:
NA.24

grade

analytical standard

Quality Level

100

Assay

≥98.0% (sum of enantiomers, GC)

optical activity

[α]20/D -88±2°, c = 1 in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.501

density

0.959 g/mL at 20 °C (lit.)

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

neat

storage temp.

2-8°C

SMILES string

CC(=C)[C@H]1CCC(CO)=CC1

InChI

1S/C10H16O/c1-8(2)10-5-3-9(7-11)4-6-10/h3,10-11H,1,4-7H2,2H3/t10-/m1/s1

InChI key

NDTYTMIUWGWIMO-SNVBAGLBSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCC7175
063264/1
63264/1

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John L Clifford et al.
Cancer prevention research (Philadelphia, Pa.), 3(2), 132-135 (2010-01-28)
This perspective on Stratton et al. (beginning on p. 160), Kowalczyk et al. (beginning on p. 170), and Katiyar et al. (beginning on p. 179) highlights the common theme of translational investigation of natural substances and their molecular effects and
Tabetha Sundin et al.
Molecular and cellular biochemistry, 375(1-2), 97-104 (2013-01-04)
We previously demonstrated in prostate cancer cells that a phytochemical-perillyl alcohol-and the mechanistic target of rapamycin (mTOR) inhibitor rapamycin rapidly attenuated telomerase activity. Protein levels of the telomerase catalytic subunit reverse transcriptase (hTERT) were diminished in the absence of an
Donghak Kim et al.
Biotechnology letters, 31(9), 1427-1431 (2009-05-22)
The catalytic turnover of cytochrome P450( cam ) from Pseudomonas putida requires two auxiliary reduction partners, putidaredoxin (Pd) and putidaredoxin reductase (PdR). We report the functional expression in Escherichia coli of tricistronic constructs consisting of P450( cam ) encoded by
Nonmelanoma skin cancer chemoprevention.
Renata Prado et al.
Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.], 37(11), 1566-1578 (2011-09-08)
Juliana de Saldanha da Gama Fischer et al.
Journal of experimental therapeutics & oncology, 7(4), 285-290 (2009-02-21)
Perillyl alcohol (POH) is a naturally occurring monoterpene with antiangiogenic and anti-tumoral properties. This chemotherapeutic agent has proven effectiveness in several clinical trials, including an ongoing phase I, comprising patients with recurrent glioblastoma multiform (GBM) under treatment with POH by
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