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155911-16-3

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155911-16-3 Usage

Description

6-HEX, also known as 6-hexanol, is a colorless liquid with a strong, sweet, herbaceous odor. It is a six-carbon alcohol with a molecular formula of C6H14O. 6-HEX is recognized for its role in creating pleasant scents and flavors, making it a valuable ingredient in various consumer products.

Uses

Used in Food Industry:
6-HEX is used as a flavoring agent for its sweet, herbaceous aroma, enhancing the taste and smell of various food products.
Used in Cosmetic Industry:
6-HEX is used as a fragrance ingredient in cosmetics, contributing to the pleasant scent of products such as perfumes, lotions, and other personal care items.
Used in Perfumery:
6-HEX is used as a component in perfumes due to its strong, sweet, and herbaceous odor, which helps create complex and appealing fragrances.
Used in Insect Attraction:
6-HEX is used in agricultural applications for attracting insects, which aids in pollination processes, as it is a volatile compound naturally emitted by plants.
Used in Essential Oils:
6-HEX is found in essential oils such as lavender and coriander, where it contributes to the overall scent profile and potential therapeutic properties of these oils.
Safety Note:
While 6-HEX is considered relatively low in toxicity, it is important to note that exposure to high concentrations may cause irritation to the eyes, skin, and respiratory system. Proper handling and usage guidelines should be followed to ensure safety.

Check Digit Verification of cas no

The CAS Registry Mumber 155911-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,9,1 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 155911-16:
(8*1)+(7*5)+(6*5)+(5*9)+(4*1)+(3*1)+(2*1)+(1*6)=133
133 % 10 = 3
So 155911-16-3 is a valid CAS Registry Number.

155911-16-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2',4,4',5',7,7'-hexachloro-3',6'-dihydroxy-1-oxospiro[2-benzofuran-3,9'-xanthene]-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2',4,4',5',7,7'-Hexachloro-3',6'-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9'-xanthene]-6-carboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:155911-16-3 SDS

155911-16-3Relevant articles and documents

Synthesis, spectroscopic properties, and biological applications of eight novel chlorinated fluorescent proteins-labeling probes

Wu, Xianglong,Tian, Min,Fan, Wutu,Pan, Yalei,Zhai, Yuankun,Niu, Yinbo,Li, Chenrui,Lu, Tingli,Mei, Qibing

, p. 775 - 786 (2014/07/22)

Eight novel chlorinated fluorescent proteins-labeling probes with a linker and reactive group were prepared in 7 steps by the reaction of chlorinated resorcinols with 3, 6-dichloro-4-carboxyphthalic anhydride in the presence of methanesulfonic acid. Structures of target compounds and intermediates were determined via IR, MS, 1H NMR and element analysis. The spectral properties of the chlorinated fluoresceins were studied. These fluorescent probes showed absorbance peaks at 508-536 nm and fluorescence peaks at 524-550 nm. It was found that they have absorption and emission maxima at long wavelengths and high fluorescence quantum yields. Emission spectra of chlorinated fluoresceins shifted towards long wavelength with increase in chlorine. The probes were used for fluorescence imaging of cells in order to investigate whether they can conjugate to cells. The fluorescence imaging of living cells showed that they were localized in cell nucleus. However, they were localized in cytosol of chemically fixed cells. These probes will be useful reagents for the preparation of stable fluorescent conjugates.

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