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V 6133, also known as 2,3-dihydroxybenzoic acid, is a phenolic acid compound that can be found in various plant sources such as fruits, vegetables, and grains. It is also produced synthetically for a range of industrial applications. V 6133 is recognized for its antioxidant properties and potential uses in cosmetics, pharmaceuticals, and food preservation. Its versatility and health-promoting properties make it a promising compound for various applications. Furthermore, V 6133 has demonstrated potential for medical applications due to its anti-inflammatory and antimicrobial effects.

70386-40-2

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70386-40-2 Usage

Uses

Used in Cosmetics Industry:
V 6133 is used as an antioxidant in cosmetics for its ability to protect the skin from oxidative stress and environmental damage, promoting healthier and more youthful-looking skin.
Used in Pharmaceuticals:
V 6133 is used as a pharmaceutical ingredient for its potential health-promoting properties, including its antioxidant, anti-inflammatory, and antimicrobial effects, which can contribute to the development of new treatments and therapies.
Used in Food Preservation:
V 6133 is used as a preservative in the food industry to extend the shelf life of products and maintain their quality by preventing oxidation and spoilage.
Used in Medical Applications:
V 6133 is used in medical applications for its potential to treat various conditions due to its anti-inflammatory and antimicrobial properties, offering new possibilities for therapeutic interventions.

Check Digit Verification of cas no

The CAS Registry Mumber 70386-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,3,8 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70386-40:
(7*7)+(6*0)+(5*3)+(4*8)+(3*6)+(2*4)+(1*0)=122
122 % 10 = 2
So 70386-40-2 is a valid CAS Registry Number.

70386-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Hydrazinecarbothioamide, 2,2'-[1-[1-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethyl] -1,2-ethanediylidene]bis- (9CI)_ V 6133 Tai-Ding-An_ Phthiobuzone

1.2 Other means of identification

Product number -
Other names -

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:70386-40-2 SDS

70386-40-2Downstream Products

70386-40-2Relevant academic research and scientific papers

Preparation method of ftibamzone

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, (2021/02/10)

The invention discloses a preparation method of ftibamzone. The preparation method comprises the following steps: firstly, preparing 3-phthalimide butanone from phthalimide potassium salt and 3-chlorobutanone; reacting the 3-phthalimide butanone with dry hydrogen bromide gas in a dimethyl sulfoxide solution to prepare a dimethyl sulfoxide solution of 3-phthalimide-2-oxy-n-butyraldehyde; dropwise adding a thiosemicarbazide solution into the dimethyl sulfoxide solution of the 3-phthalimide-2-oxy-n-butyraldehyde, controlling the reaction temperature, carrying out heat preservation reaction to prepare a crude product, and recrystallizing the crude product to obtain the ftibamzone. The technical scheme has the advantages of few reaction steps, high yield and high purity.

Preparation method of 3-phthalimide-2-oxy-n-butyraldehyde thiosemicarbazide

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, (2019/08/12)

The invention relates to a preparation method of 3-phthalimide-2-oxy-n-butyraldehyde thiosemicarbazide (I). The preparation method comprises the steps: adopting alanine and N-ethoxycarbonyl phthalimide as a starting material, and performing aminoacylation, methyl-lithium addition, an oxidation reaction and a condensation reaction so as to obtain the target product 3-phthalimide-2-oxy-n-butyraldehyde thiosemicarbazide (I). The method for synthesizing 3-phthalimide-2-oxy-n-butyraldehyde thiosemicarbazide has the advantages of few reaction steps, simple operation, suitability for large-scale production and the like.

Method for synthesizing 3 - phthalatic imide - 2 - oxo-butyl - 1, 2 - double-thiosemicarbazone method

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, (2017/04/12)

The invention relates to a novel method of synthesizing 3-phthalimide-2-oxobutryaldehyde-1, 2-bis-thiosemicarbazide. The novel method comprises the following steps: synthesizing 3-nitro-2-butanol with acetaldehyde and nitroethane as starting raw materials, then carrying out reduction on 3-nitro-2-butanol to generate 3-amino-2-butanol, carrying out reaction on 3-amino-2-butanol and phthalic anhydride to generate N-(1-methyl-2-hydroxypropyl) phthalimide, respectively carrying out oxidation by two steps to form 3-phthalimide-2-oxo-butyraldehyde, and finally carrying out condensation on 3-phthalimide-2-oxo-butyraldehyde and thiosemicarbazide to obtain a target product. The 3-phthalimide-2-oxobutryaldehyde-1, 2-bis-thiosemicarbazide has obvious inhibition action on replication of herpes simplex I type (HSV-I) and II I type (HSV-II) viruses in tissue culture cells; at present, the 3-phthalimide-2-oxobutryaldehyde-1, 2-bis-thiosemicarbazide is mainly clinically used for treating skin diseases caused by herpesvirus and sexually transmitted diseases caused by human papillomavirus (HSV) and has good curative effect.

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