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| Product | Description | |
|---|---|---|
| acetolactate decarboxylase | This enzyme belongs to the family of lyases, specifically the carboxy-lyases, which cleave carbon-carbon bonds. This enzyme participates in butanoate metabolism and c5-branched dibasic acid metabolism. Group: Enzymes. Synonyms: α-acetolactate decarboxylase; (S)-2-hydroxy-2-methyl-3-oxobutanoate carboxy-lyase; (S)-2-hydroxy-2-methyl-3-oxobutanoate carboxy-lyase [(R)-2-acetoin-forming]; (S)-2-hydroxy-2-methyl-3-oxobutanoate carboxy-lyase [(3R)-3-hydroxybutan-2-one-forming]. Enzyme Commission Number: EC 4.1.1.5. CAS No. 9025-2-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4795; acetolactate decarboxylase; EC 4.1.1.5; 9025-02-9; α-acetolactate decarboxylase; (S)-2-hydroxy-2-methyl-3-oxobutanoate carboxy-lyase; (S)-2-hydroxy-2-methyl-3-oxobutanoate carboxy-lyase [(R)-2-acetoin-forming]; (S)-2-hydroxy-2-methyl-3-oxobutanoate carboxy-lyase [(3R)-3-hydroxybutan-2-one-forming]. Cat No: EXWM-4795. |  |
| α-acetolactate decarboxylase | An alpha-acetolactate decarboxylase that bypasses production of diacetyl, converting alpha-acetolactate to acetoin, which reduces maturation time and improves taste, color and aroma. Applications: Chill-proofing and maturation. Group: Enzymes. Synonyms: alpha-acetolactate decarboxylase; Chill-proofing enzyme; Maturation enzyme; Brewing; alpha-acetolactate decarboxylase; BRE-1621. CAS No. 9025-2-9. α-acetolactate decarboxylase. Appearance: powder or liquid. alpha-acetolactate decarboxylase; Chill-proofing enzyme; Maturation enzyme; Brewing; alpha-acetolactate decarboxylase; BRE-1621. Pack: 25kg/paper barrel (powder form), 30kg/polyster barrel (liquid form) or subject to client requirement. Cat No: BRE-1621. | |
| (2R,3R)-2-Methylbutane-1,2,3-triol | (2R,3R)-2-Methylbutane-1,2,3-triol is an intermediate in the synthesis of (S)-α-Acetolactic Acid (A163805), one of the enantiomers of acetolactate, which is the substrate of Acetolactate decarboxylase, which catalyzes the conversion of both enantiomers of acetolactate to the (R)-enantiomer of acetoin. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 100mg, 250mg. Molecular Formula: C5H12O3. US Biological Life Sciences. |  Worldwide |
| (2S)-2-Hydroxy-2-methyl-3-oxobutanoic Acid Phenylmethyl Ester | (2S)-2-Hydroxy-2-methyl-3-oxobutanoic Acid Phenylmethyl Ester is an intermediate in the synthesis of (S)-α-Acetolactic Acid (A163805), one of the enantiomers of acetolactate, which is the substrate of Acetolactate decarboxylase, which catalyzes the conversion of both enantiomers of acetolactate to the (R)-enantiomer of acetoin. Group: Biochemicals. Grades: Highly Purified. CAS No. 442159-35-5. Pack Sizes: 100mg, 250mg. Molecular Formula: C12H14O4. US Biological Life Sciences. | Worldwide |
| (S)-α-Acetolactic Acid Potassium Salt | (S)-α-Acetolactic Acid, is one of the enantiomers of acetolactate, which is the substrate of Acetolactate decarboxylase, which catalyzes the conversion of both enantiomers of acetolactate to the (R)-enantiomer of acetoin. Group: Biochemicals. Alternative Names: (2S)-2-Hydroxy-2-methyl-3-oxo-butanoic Acid Potassium Salt. Grades: Highly Purified. CAS No. 71698-08-3. Pack Sizes: 5mg. Molecular Formula: C?H?KO?, Molecular Weight: 170.2. US Biological Life Sciences. | Worldwide |
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