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D-valine dane salt is a chemical compound that combines D-valine, a non-essential amino acid, with a salt component. It is a vital constituent in the structure of many proteins and is important for the proper functioning of the nervous system. The addition of a salt component to D-valine enhances its solubility and stability, making it easier to store and handle in laboratory settings.

134841-35-3

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134841-35-3 Usage

Uses

Used in Pharmaceutical Industry:
D-valine dane salt is used as an active pharmaceutical ingredient for its role in protein synthesis and its potential therapeutic applications in nervous system disorders.
Used in Food Additives Industry:
D-valine dane salt is used as a flavor enhancer and nutritional supplement in food products, contributing to the amino acid profile and improving taste.
Used in Biochemical Research:
D-valine dane salt is used as a research tool in biochemical studies, facilitating experiments related to protein structure, function, and synthesis. Its enhanced solubility and stability make it an ideal compound for laboratory use.

Check Digit Verification of cas no

The CAS Registry Mumber 134841-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,8,4 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 134841-35:
(8*1)+(7*3)+(6*4)+(5*8)+(4*4)+(3*1)+(2*3)+(1*5)=123
123 % 10 = 3
So 134841-35-3 is a valid CAS Registry Number.

134841-35-3Downstream Products

134841-35-3Relevant academic research and scientific papers

Synthesis method of valnemulin hydrochloride

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Paragraph 0063-0065; 0076-0078; 0089; 0090; 0102; 0103, (2017/04/03)

The invention discloses a synthesis method of valnemulin hydrochloride. The synthesis method comprises the following three steps: synthesis of dimethylcysteamine pleuromulin from pleuromulin, synthesis of D-valine dane salt from D-valine and synthesis of

Process for the preparation of pleuromutilins

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Page/Page column 7, (2008/06/13)

A process for the preparation of 14-O-[(N-(3-methyl-2-amino-butyryl-piperidinyl)sulfanyl) acetyl]mutilins of formula feasible for large-scale production of high purity products, and wherein the carbon atom at the piperidine ring attached to the sulphur atom is either in the (S)-configuration or in the (R)-configuration, and a new crystalline form of 14-O-[(N-3-methyl-2-(R)-amino-butyryl-piperidine-3(S)-yl)sulfanyl)acetyl]mutilin - hydrochloride.

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