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Merck
모든 사진(1)

주요 문서

63661

Supelco

(+)-Menthofuran

analytical standard

동의어(들):

(6R)-4,5,6,7-Tetrahydro-3,6-dimethylbenzofuran, (R)-3,6-Dimethyl-4,5,6,7-tetrahydrobenzofuran

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About This Item

실험식(Hill 표기법):
C10H14O
CAS Number:
Molecular Weight:
150.22
Beilstein:
2729
MDL number:
UNSPSC 코드:
85151701
PubChem Substance ID:
NACRES:
NA.24

Grade

analytical standard

Quality Level

분석

≥99.0% (sum of enantiomers, GC)

광학 활성

[α]20/D +100±2°, neat

유통기한

limited shelf life, expiry date on the label

기술

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.484

bp

204-206 °C (lit.)

density

0.97 g/mL at 20 °C (lit.)

응용 분야

food and beverages

형식

neat

저장 온도

2-8°C

SMILES string

C[C@@H]1CCc2c(C)coc2C1

InChI

1S/C10H14O/c1-7-3-4-9-8(2)6-11-10(9)5-7/h6-7H,3-5H2,1-2H3/t7-/m1/s1

InChI key

YGWKXXYGDYYFJU-SSDOTTSWSA-N

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일반 설명

(+)-Menthofuran is a metabolite of pulegone, found in mint plants, which is basically produced from (+)–pulegone by menthofuran synthase enzyme, under certain conditions of stress like low sunlight, limited moisture and nutrient deficiencies.

애플리케이션

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

기타 정보

This compound is commonly found in plants of the genus: mentha

픽토그램

Exclamation markEnvironment

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves


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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

이미 열람한 고객

Council of Europe
Chemically-defined Flavouring Substances (2000)
Rahman-U-A
Studies in Natural Products Chemistry, Volume 37, 37 (2012)
(R)-(+)-Menthofuran is a potent, mechanism-based inactivator of human liver cytochrome P450 2A6
Khojasteh - Bakht.CS
Drug Metabolism and Disposition, 26(7), 701-704 (1998)
Soheil S Mahmoud et al.
Proceedings of the National Academy of Sciences of the United States of America, 100(24), 14481-14486 (2003-11-19)
(+)-Pulegone is a central intermediate in the biosynthesis of (-)-menthol, the most significant component of peppermint essential oil. Depending on environmental conditions, this branch point metabolite may be reduced to (-)-menthone en route to menthol, by pulegone reductase (PR), or
P Racine et al.
Fitoterapia, 76(3-4), 316-323 (2005-05-14)
The quenching activity against singlet oxygen, an actor of lipid peroxidation and DNA degradation, of the essential oil and resinoid of Commiphora myrrha from Somalia has been studied and compared to DL-alpha-tocopherol using 1,3-diphenylisobenzofuran (DPBF) as a probe. To insure

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