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Sodium DL-Malate, a chemical compound derived from malic acid, is commonly found in various fruits such as apples. It is recognized for its sour taste and buffering properties, which make it a versatile ingredient in the food, cosmetic, and pharmaceutical industries. Sodium DL-Malate is generally recognized as safe for consumption by the FDA, and its applications extend beyond food products to include health and wellness benefits.

676-46-0

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676-46-0 Usage

Uses

Used in the Food Industry:
Sodium DL-Malate is used as a flavor enhancer and preservative for its ability to add a sour taste and control the acidity of food products, thereby improving the overall taste and stability of various food items.
Used in the Cosmetic Industry:
In the cosmetic sector, Sodium DL-Malate is utilized as a buffering agent and pH adjuster, ensuring the stability and effectiveness of cosmetic formulations.
Used in the Pharmaceutical Industry:
Sodium DL-Malate is employed in the production of pharmaceuticals, where it serves as a buffering agent to maintain the desired pH levels in medications, thus ensuring their efficacy and safety.
Used in Metabolic Disorder Treatment:
Sodium DL-Malate is used in the treatment of metabolic disorders, as it plays a role in the body's energy production and metabolic processes, helping to regulate and support overall health.
Used as an Energy Source:
Sodium DL-Malate also serves as a source of energy for the body, contributing to the maintenance of vital physiological functions and supporting overall well-being.

Check Digit Verification of cas no

The CAS Registry Mumber 676-46-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,7 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 676-46:
(5*6)+(4*7)+(3*6)+(2*4)+(1*6)=90
90 % 10 = 0
So 676-46-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H6O5.Na/c5-2(4(8)9)1-3(6)7;/h2,5H,1H2,(H,6,7)(H,8,9);

676-46-0 Well-known Company Product Price

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  • Aldrich

  • (M6773)  DL-Malicaciddisodiumsalt  ≥95% (capillary GC)

  • 676-46-0

  • M6773-5G

  • 321.75CNY

  • Detail
  • Aldrich

  • (M6773)  DL-Malicaciddisodiumsalt  ≥95% (capillary GC)

  • 676-46-0

  • M6773-25G

  • 996.84CNY

  • Detail

676-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Sodium 2-hydroxysuccinate

1.2 Other means of identification

Product number -
Other names Sodium DL-Malate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives
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:676-46-0 SDS

676-46-0Downstream Products

676-46-0Relevant academic research and scientific papers

Process for preparing hyperpolarized substrates and method for MRI

-

Page/Page column 35, (2017/08/01)

The present invention generally relates to a process for the preparation of aqueous solutions of hyperpolarized molecules ready for use in in-vivo MR diagnostic imaging, the use thereof as MRI contrast agent in investigation methods for producing diagnostic MR images of a human or non-human animal body organ, region or tissue.

Sulfonamide derivatives

-

Page 8-12, (2010/02/05)

The present invention relates to a compound of formula (I) or a pharmaceutically acceptable salt thereof which is useful for the treatment of conditions associated with glutamate hypofunction, such as psychiatric and neurological disorders.

Enzymatic Production of L-Malate from Maleate by Alcaligenes sp.

Kimura, Takuhei,Kawabata, Yasuro,Sato, Eiji

, p. 89 - 94 (2007/10/02)

Alcaligenes sp.T501, which has the ability to produce L-malate from maleate at a concentration of 20percent in a molar yield of 98.4percent was isolated from soil.Analysis of the reaction mixture components suggested that maleate was converted to L-malate via fumarate through the action of maleate isomerase and fumarase.These two enzymes were constitutively found in the cells regardless of the carbon source in the medium.The enzyme reaction was significantly enhanced by adding 2-mercaptoethanol, but was not affected by glutathione or L-cysteine.

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