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Home > Encyclopedia > DL-Glutamic acid, monosodium salt

DL-Glutamic acid, monosodium salt

pharmaceutical raw materials
DL-Glutamic acid, monosodium salt structure

DL-Glutamic acid, monosodium salt 

structure
  • CAS No:

    32221-81-1

  • Formula:

    C5H9NO4.Na

  • Chemical Name:

    DL-Glutamic acid, monosodium salt

  • Synonyms:

    Glutamic acid,sodium salt (1:1);Glutamic acid,monosodium salt,DL-;DL-Glutamic acid,monosodium salt;Glutamic acid,monosodium salt;Monosodium DL-glutamate;Monosodium DL-glutamate

  • Categories:

    Cosmetic Ingredient  >  Hair Conditioning

Description

white crystalline solid


A peptide that is a homopolymer of glutamic acid.

DL-Glutamic acid, monosodium salt Basic Attributes

169.11109

187.045670

205-538-1

DTXSID4020905

2103901000

Characteristics

103.45000

-1.37130

Monosodium glutamate appears as white or off-white crystalline powder with a slight peptone-like odor. pH (0.2% solution)7.0. (NTP, 1992)

26.2 (saturated water solution at 20 °C)

450 °F (Decomposes) (NTP, 1992)

333.8ºC at 760 mmHg

155.7ºC

greater than or equal to 100 mg/mL at 68° F (NTP, 1992)

[α]D/20 between + 24,8° and + 25,3°; (10 % solution (anhydrous basis) in 2N HCl, 200 mm tube)

Practically odorless

Meaty taste comes from contaminants in crude glutamates; sweet-saline taste in large concn; no flavor in small quantity

Between 6,7 and 7,2 (5 % solution)

Safety Information

Stable. Incompatible with strong oxidizing agents

Drug Information

Polyglutamate

DL-Glutamic acid, monosodium salt Use and Manufacturing

Methods of Manufacturing

At present, both domestic and foreign countries use rice, starch or molasses as raw materials to produce through saccharification, fermentation, extraction and refining processes: (1) Saccharification of starch. The saccharification of starch mostly adopts the double enzyme method. Rice is soaked, sand-milled or starch is directly blended into starch slurry with relative density of 1.11 (14°Bé), and α-amylase is added to liquefy 15-20min under the condition of pH 4.5 and 90°C, and then heated to 100°C to kill enzyme 5min; After discharging, filter by plate and frame, the filter residue can be used as feed, the filtrate is adjusted to PH5.0, β-amylase is added, saccharification at 60℃ for 12h, and then heated to 100℃ to kill the enzyme and cool and clarify, the supernatant Put it directly into the sugar storage tank, add the filter aid diatomaceous earth to the sedimentation liquid and press filter, the starch sugar conversion rate can reach 92%. (2) Glutamate fermentation. Use about 15% glucose as the carbon source, and add appropriate amount of inorganic salt and biotin to prepare the fermentation medium. After continuous digestion and cooling to 40℃, it is sent to the sterilized empty fermentation tank, and the liquid ammonia is added. As a nitrogen source, it is inoculated with glutamic acid-producing bacteria that has undergone secondary expansion culture. After 30 hours of aeration fermentation, the sugar-acid conversion rate can reach 50% and the acid production level is about 7.0%-7.5%. The pH of the fermentation process is controlled at 7.0-7.2, and the temperature is controlled at 32-34°C in the early stage and 34-37°C in the later stage. (3) Extraction of glutamic acid. The extraction of glutamic acid generally uses the freezing isoelectric-ion exchange method. The fermentation broth was slowly stirred with frozen brine in an isoelectric tank to cool down to 5°C, while adjusting the pH to 3.22 (isoelectric point) with sulfuric acid; after 8h of precipitation, the precipitate was centrifuged to obtain crude glutamic acid; mother liquor and supernatant After liquid preparation, it is exchanged with ion exchange resin and dewashed with ammonia water; the front fraction is merged into the supernatant and re-loaded on the column, the latter fraction is used as the eluent together with the ammonia water, and the high fraction is returned to the isoelectric tank together with the fermentation broth for extraction The rate can reach 88%-90%. (4) Refining of glutamic acid. Add glutamic acid to a neutralization tank with 60-65℃ bottom water, stir, and slowly add soda ash solution to neutralize to pH 6.2-6.4, and control the concentration of the neutralization solution to a relative density of 1.17-1.18 (21- 22°Bé); After the neutralization solution is cooled to below 50°C, add an appropriate amount of sodium sulfide solution to remove iron, then use crude glutamic acid to adjust the pH to 6.2-6.4, and heat to 60°C, then add powdered activated carbon and stir After 0.5h, it is sent to a filter press and filtered, and then the filtrate is decolorized with a granular activated carbon column to obtain a clear liquid; the clear liquid is sent to a vacuum crystal boiling pot and evaporated and concentrated to a relative density of 1.28 (31.5°Bé) at 60-70°C After adding 0.36-0.542mm seed crystals, continue to evaporate and crystallize. During this period, hot water is required to kill the crystals and add a certain amount of clear liquid; after discharging, the crystal is incubated in a crystal tank and centrifuged to obtain crystalline monosodium glutamate. The mother liquor may be decolorized After evaporation and crystallization, the refining yield can reach 92% of the theoretical amount.

Uses

Sodium glutamate is the most widely used umami agent at home and abroad. It can enhance its taste effect when coexisting with table salt. It is more synergistic when used together with sodium 5'-inosinate or sodium 5'-guanylate effect. Our country stipulates that it can be used in all kinds of food in appropriate amounts according to production needs. Used as a food flavoring agent

Computed Properties

Molecular Weight:169.11
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:169.03510202
Monoisotopic Mass:169.03510202
Topological Polar Surface Area:103
Heavy Atom Count:11
Complexity:149
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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