Category:information only not used for fragrances or flavors
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Physical Properties:
Appearance: | colorless to pale yellow clear liquid (est) |
Assay: | 95.00 to 100.00
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Food Chemicals Codex Listed: | No |
Melting Point: | 33.00 °C. @ 760.00 mm Hg
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Boiling Point: | 183.50 °C. @ 760.00 mm Hg
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Vapor Pressure: | 0.380000 mmHg @ 25.00 °C. |
Flash Point: | 185.00 °F. TCC ( 85.00 °C. )
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logP (o/w): | -0.655 (est) |
Soluble in: |
| alcohol | | water, 1.00E+06 mg/L @ 20 °C (exp) |
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found). |
Cosmetic Information:
Suppliers:
Safety Information:
Preferred SDS: View |
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Hazards identification |
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Classification of the substance or mixture |
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) |
None found. |
GHS Label elements, including precautionary statements |
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Pictogram | |
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Hazard statement(s) |
None found. |
Precautionary statement(s) |
None found. |
Oral/Parenteral Toxicity: |
Not determined
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Dermal Toxicity: |
Not determined
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Inhalation Toxicity: |
Not determined
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Safety in Use Information:
Category: | information only not used for fragrances or flavors |
Recommendation for meso-2,3-butane diol usage levels up to: | | not for fragrance use.
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Recommendation for meso-2,3-butane diol flavor usage levels up to: |
| not for flavor use.
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Safety References:
References:
Other Information:
Potential Blenders and core components note
Potential Uses:
Occurrence (nature, food, other): note
Synonyms:
(2R,3S)- | butane-2,3-diol | (2R,3S)-rel-2,3- | butanediol | meso-2,3- | butanediol | 2,3- | butanediol (meso) | 2,3- | butanediol, (2R,3S)- | 2,3- | butanediol, (R*, S*)- | 2,3- | butanediol, meso- | | erythro-2,3-butane diol |
Articles:
PubMed:2-Butanol and Butanone Production in Saccharomyces cerevisiae through Combination of a B12 Dependent Dehydratase and a Secondary Alcohol Dehydrogenase Using a TEV-Based Expression System. |
PubMed:Cloning, expression and characterization of glycerol dehydrogenase involved in 2,3-butanediol formation in Serratia marcescens H30. |
PubMed:Genome Sequence of meso-2,3-Butanediol-Producing Strain Serratia marcescens ATCC 14041. |
PubMed:Mechanism of 2,3-butanediol stereoisomer formation in Klebsiella pneumoniae. |
PubMed:Deletion of meso-2,3-butanediol dehydrogenase gene budC for enhanced D-2,3-butanediol production in Bacillus licheniformis. |
PubMed:Glycerol dehydrogenase plays a dual role in glycerol metabolism and 2,3-butanediol formation in Klebsiella pneumoniae. |
PubMed:Efficient bioconversion of 2,3-butanediol into acetoin using Gluconobacter oxydans DSM 2003. |
PubMed:Synthesis of 2,3-butanediol by Synechocystis sp. PCC6803 via heterologous expression of a catabolic pathway from lactic acid- and enterobacteria. |
PubMed:Improved cellobiose utilization in E. coli by including both hydrolysis and phosphorolysis mechanisms. |
PubMed:A newly isolated Bacillus licheniformis strain thermophilically produces 2,3-butanediol, a platform and fuel bio-chemical. |
PubMed:Enantiomeric recognition of amino acid salts by macrocyclic crown ethers derived from enantiomerically pure 1,8,9,16-tetrahydroxytetraphenylenes. |
PubMed:A new NAD(H)-dependent meso-2,3-butanediol dehydrogenase from an industrially potential strain Serratia marcescens H30. |
PubMed:High-yield production of meso-2,3-butanediol from cellodextrin by engineered E. coli biocatalysts. |
PubMed:Cloning, expression and characterization of meso-2,3-butanediol dehydrogenase from Klebsiella pneumoniae. |
PubMed:Synthesis of pure meso-2,3-butanediol from crude glycerol using an engineered metabolic pathway in Escherichia coli. |
PubMed:Aromatic compounds from the halotolerant fungal strain of Wallemia sebi PXP-89 in a hypersaline medium. |
PubMed:Characterization of a zinc-containing alcohol dehydrogenase with stereoselectivity from the hyperthermophilic archaeon Thermococcus guaymasensis. |
PubMed:D-2,3-butanediol production due to heterologous expression of an acetoin reductase in Clostridium acetobutylicum. |
PubMed:Relationship between changes in the total concentration of acetic acid bacteria and major volatile compounds during the acetic acid fermentation of white wine. |
PubMed:Microbial production of meso-2,3-butanediol by metabolically engineered Escherichia coli under low oxygen condition. |
PubMed:Metabolic engineering of acetoin and meso-2, 3-butanediol biosynthesis in E. coli. |
PubMed:Effects of straight chain alcohols on specific isoforms of adenylyl cyclase. |
PubMed:Role of Saccharomyces cerevisiae oxidoreductases Bdh1p and Ara1p in the metabolism of acetoin and 2,3-butanediol. |
PubMed:From simple diols to carbohydrate derivatives of phenylarsonic acid. |
PubMed:Determination of 2,3-butanediol and 2-hydroxybutanone stereoisomers in batteries of traditional balsamic vinegar. |
PubMed:Fermentation product butane 2,3-diol induces Ca2+ transients in E. coli through activation of lanthanum-sensitive Ca2+ channels. |
PubMed:Male-specific EAD active compounds produced by female European chafer Rhizotrogus majalis (Razoumowsky). |
PubMed:Chiral direction and interconnection of helical three-connected networks in metal-organic frameworks. |
PubMed:Ab initio conformational studies on diols and binary diol-water systems using DFT methods. Intramolecular hydrogen bonding and 1:1 complex formation with water. |
PubMed:Crystallization and preliminary X-ray studies of meso-2,3-butanediol dehydrogenase from Klebsiella pneumoniae IAM1063. |
PubMed:Crystal structure of meso-2,3-butanediol dehydrogenase in a complex with NAD+ and inhibitor mercaptoethanol at 1.7 A resolution for understanding of chiral substrate recognition mechanisms. |
PubMed:Structural analysis of diols by electrospray mass spectrometry on boric acid complexes. |
PubMed:Production of 2,3-butanediol by newly isolated Enterobacter cloacae. |
PubMed:Separation of racemic from meso-2,3-butanediol |
PubMed:Formation of a chiral acetoinic compound from diacetyl by Escherichia coli expressing meso-2,3-butanediol dehydrogenase. |
PubMed:The production of D-acetoin by a transgenic Escherichia coli. |
PubMed:An electron paramagnetic resonance study on the mechanism-based inactivation of adenosylcobalamin-dependent diol dehydrase by glycerol and other substrates. |
PubMed:Metabolism of 2,3-butanediol stereoisomers in the perfused rat liver. |
PubMed:Enantio- and regioselectivity in the epoxide-hydrolase-catalyzed ring opening of aliphatic oxiranes: Part II: Dialkyl- and trialkylsubstituted oxiranes. |
PubMed:Properties of 2,3-Butanediol Dehydrogenases from Lactococcus lactis subsp. lactis in Relation to Citrate Fermentation. |
PubMed:Assay of physiological levels of 2,3-butanediol diastereomers in blood and urine by gas chromatography-mass spectrometry. |
PubMed:Short chain diol metabolism in human disease states. |
PubMed:The measurement of 1,2-propanediol, D, L-2,3-butanediol and meso-2,3-butanediol in controls and alcoholic cirrhotics. |
PubMed:Electron-capture, capillary column gas chromatographic determination of low-molecular-weight diols in serum. |
PubMed:Production of 2-butanol through meso-2,3-butanediol consumption in lactic acid bacteria. |
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