L-Aspartic Acid

L-Aspartic Acid

L-Aspartic acid · C4H7NO4

L-Aspartic acid powder, CAS 56-84-8, made by enzymatic amination of fumaric acid and assayed 98.5-101.5% dried basis. Acidic amino acid for chelates, aspartame and effervescent blends.

Specifications

Chemical nameL-Aspartic acid; (2S)-2-aminobutanedioic acid
CAS number56-84-8
Molecular formula / weightC4H7NO4 / 133.10 g/mol
AppearanceWhite crystals or crystalline powder with a slightly acidic taste; decomposes on heating at approximately 270 deg C
Assay (dried basis)98.5 - 101.5 % C4H7NO4 by titration with 0.1 M sodium hydroxide, to the USP monograph range
Specific optical rotation+24.5 deg to +26.0 deg, calculated on the dried basis, to the USP monograph range; confirms the L-enantiomer against D- and DL-forms
SolubilitySlightly soluble in water, approximately 5 g/L at 25 deg C; freely soluble in dilute mineral acid and in alkali hydroxide solution
Loss on drying / residue on ignitionControlled to the USP and Ph. Eur. monograph limits; the measured value for each lot is reported on the batch CoA
Elemental impuritiesLead, arsenic, cadmium and mercury tested against ICH Q3D and monograph limits; results reported per batch
Source and production routeEnzymatic amination of fumaric acid with L-aspartate ammonia-lyase (aspartase, EC 4.3.1.1) on immobilised microbial cells; no animal input
Allergen statusFree from milk, egg, soy, fish, crustacean, gluten, peanut and tree nut; synthesised from fumaric acid and ammonia, not from any protein hydrolysate
Dietary and origin suitabilityVegan and vegetarian suitable; non-bovine, non-porcine and non-marine. Non-GMO declaration, Kosher and Halal certificates on request
Shelf life and storageTypically 24 - 36 months from manufacture in unopened original packing; store below 25 deg C, dry and away from direct sunlight
HS code (India)2922 49 90, not 2922 50 90 - only one kind of oxygen function is present; see classification note
L-Aspartic acid is (2S)-2-aminobutanedioic acid, CAS 56-84-8, molecular formula C4H7NO4 and molecular weight 133.10. It is one of the two acidic, dicarboxylic proteinogenic amino acids, carrying a second carboxyl group on the beta carbon, and that extra acid function drives almost everything a formulator needs to know about it. The material is only slightly soluble in plain water, around 5 g/L at 25 degrees C, yet dissolves freely in dilute mineral acid and in alkali hydroxide solution, so wet-process work is normally done as the salt or under pH control rather than by trying to dissolve the free acid. It presents as white crystals or crystalline powder with a slightly acidic taste, decomposes on heating at about 270 degrees C, and is held to the USP content range of 98.5 to 101.5 percent on the dried basis with a specific rotation of +24.5 to +26.0 degrees, determined by titration against 0.1 M sodium hydroxide. Aspartic acid is dietarily non-essential in humans and is formed endogenously by transamination of oxaloacetate, which places it directly at the junction between amino acid nitrogen and the tricarboxylic acid cycle; it is also the nitrogen donor entering the urea cycle at argininosuccinate. That is a statement of established intermediary metabolism and composition, not a health benefit - Thovek makes no therapeutic or disease claim for the ingredient, and any nutrient or function wording on a finished product remains the brand owner's responsibility under destination-market rules. Commercially, the ingredient is bought for three quite different reasons: as the acid partner in mineral aspartate chelates such as magnesium, zinc, potassium and calcium aspartate, as the amino acid feedstock in aspartame manufacture, and as a free-form amino acid in sports and clinical nutrition blends, where its low free-acid solubility makes it a common choice for effervescent and granulated systems. Production is enzymatic rather than fermentative or extractive. Fumaric acid and ammonia are combined using L-aspartate ammonia-lyase, the aspartase enzyme EC 4.3.1.1, carried on immobilised microbial cells in a continuous reactor - a route first commercialised in Japan and still the industry standard because it gives high product concentration with very little by-product. Nothing of animal origin is involved and the product is not a protein hydrolysate, so it is vegan and vegetarian suitable, non-bovine, non-porcine and non-marine, and free from milk, egg, soy, fish, crustacean, gluten, peanut and tree nut. Buyers should distinguish this L-form clearly from D-aspartic acid and from the DL-racemate, which are separate articles with different specifications and different optical rotation; Thovek supplies the L-enantiomer only, and the rotation figure on each CoA is the check. Batch CoA, MSDS, allergen and origin statement, non-GMO declaration and Kosher or Halal certificates accompany every consignment.

Applications

Mineral aspartate chelate manufactureAspartame synthesis feedstockEffervescent tablet blendsFree-form amino acid blendsSports nutrition formulationsCell culture media componentPolyaspartic acid productionFood acidulant and flavour

Available grades

Food grade (FCC) and pharmaceutical grade to USP / Ph. Eur. / BP / JP monograph; technical grade for polyaspartate and chelation feedstock. Standard crystalline powder, with granular and fine-milled cuts to order. L-enantiomer only - D- and DL-forms are separate articles.

Packaging: 25 kg fibre drums or multi-wall paper sacks with food-grade LDPE inner liner, heat sealed. 500 kg and 1000 kg big bags for chelation and aspartame feedstock volumes. 1 kg and 5 kg foil pouches for trials; palletised and shrink-wrapped for FCL or LCL export.

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