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DL-Malic Acid Monosodium Salt is a naturally occurring isomer of malic acid, primarily found in sour and unripe fruits. It is a white crystalline powder with a slightly acidic taste and is known for its ability to enhance the flavor and acidity of various food and beverage products.

68303-40-2

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68303-40-2 Usage

Uses

Used in Food and Beverage Industry:
DL-Malic Acid Monosodium Salt is used as a flavor enhancer for its ability to improve the taste and acidity of various food and beverage products, providing a more balanced and refreshing taste.
Used in Wine Analysis:
DL-Malic Acid Monosodium Salt is used as a component in the preparation of standard solutions during the analysis of wine samples using peroxidase-based biosensors. This application aids in the accurate measurement and analysis of malic acid content in wines, which is crucial for understanding the wine's quality and characteristics.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, DL-Malic Acid Monosodium Salt can also be used in the pharmaceutical industry for various applications, such as an intermediate in the synthesis of drugs, a buffering agent, or an additive in the formulation of certain medications. Its versatility and natural occurrence make it a valuable compound in the development of pharmaceutical products.

Check Digit Verification of cas no

The CAS Registry Mumber 68303-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,0 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 68303-40:
(7*6)+(6*8)+(5*3)+(4*0)+(3*3)+(2*4)+(1*0)=122
122 % 10 = 2
So 68303-40-2 is a valid CAS Registry Number.

68303-40-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Aldrich

  • (M1125)  L-(−)-Malicacidsodiumsalt  95-100% (enzymatic)

  • 68303-40-2

  • M1125-5G

  • 332.28CNY

  • Detail
  • Aldrich

  • (M1125)  L-(−)-Malicacidsodiumsalt  95-100% (enzymatic)

  • 68303-40-2

  • M1125-25G

  • 940.68CNY

  • Detail
  • Aldrich

  • (M1125)  L-(−)-Malicacidsodiumsalt  95-100% (enzymatic)

  • 68303-40-2

  • M1125-100G

  • 2,846.61CNY

  • Detail

68303-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name DL-MALIC ACID MONOSODIUM SALT

1.2 Other means of identification

Product number -
Other names PURASAL(R)S/SP 60

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:68303-40-2 SDS

68303-40-2Downstream Products

68303-40-2Relevant 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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