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Merck
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文件

77311

Supelco

(-)-紫苏子醇

analytical standard

别名:

(S)-4-异丙烯基-1-环己烯基甲醇, (S)-对薄荷-1,8-二烯-7-醇

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About This Item

经验公式（希尔记法）:
C10H16O
CAS号:
18457-55-1
分子量:
152.23
Beilstein:
2501605
MDL號碼:
MFCD00062995
分類程式碼代碼:
85151701
PubChem物質ID:
329767604
NACRES:
NA.24

等級

analytical standard

品質等級

100

化驗

≥98.0% (sum of enantiomers, GC)

光學活性

[α]20/D -88±2°, c = 1 in methanol

技術

HPLC: suitable
gas chromatography (GC): suitable

折射率

n20/D 1.501

密度

0.959 g/mL at 20 °C (lit.)

應用

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

格式

neat

儲存溫度

2-8°C

SMILES 字串

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 密鑰

NDTYTMIUWGWIMO-SNVBAGLBSA-N

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應用

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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Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

230.0 °F - closed cup

閃點（°C）

110 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

分析证书(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
Makoto Koyama et al.
Oncology reports, 29(2), 779-784 (2012-12-13)
The monoterpene perillyl alcohol (POH) is a naturally occurring compound derived from citrus fruits, mint and herbs. It exhibited chemotherapeutic potential against various malignant tumors in preclinical models and is currently being tested in clinical trials in patients with refractory
Francisco das Chagas Abreu da Silveira et al.
Journal of cancer research and clinical oncology, 138(8), 1347-1354 (2012-04-07)
Malignant gliomas are associated with alteration in EGF/EGFR signaling. Functional EGF+61A>G polymorphism is implicated with risk, recurrence, and progression of glioma. This study aimed to establish a putative association of EGF+61A>G with risk of glioma development, production of angiogenic growth
Ismail Kiran
Natural product communications, 6(12), 1805-1806 (2012-02-09)
S-(-)-Perillyl alcohol (p-mentha-1, 8-diene-7-ol) (1) (500 mg) was converted by Fusarium heterosporium ATCC 15625 over 10 days at 25 degrees C to a new metabolite, 1,2-dihydroxyperillyl alcohol (p-mentha-8-en-1,2,7-triol) (3) in a yield of 13% (70 mg). The structure of 3
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