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19132-06-0

19132-06-0 Structure

19132-06-0 Structure
IdentificationMore
[Name]

(S,S)-2,3-Butanediol
[CAS]

19132-06-0
[Synonyms]

2,3-BUTANEDIOL, [S-(R*,R*)]-
(2S,3S)-(+)-2,3-BUTANEDIOL
(2S,3S)-2,3-BUTANEDIOL
L(+)-2,3-BUTANEDIOL
(S,S)-(+)-2,3-BUTANEDIOL
(S,S)-2,3-BUTANEDIOL
(S,S)-(+)-2,3-BUTYLENE GLYCOL
(S,S)-(+)-2,3-DIHYDROXYBUTANE
(S-(R,R))-butane-2,3-diol
(2S,3S)-(+)-2,3-BUTANEDIOL, 97%(99% EE/GLC)
2S,3S-(+)-Butanediol
(2S,3S)-(+)-2,3-Butanediol,99%
(2S,3S)-(+)-2,3-BUTANEDIOL 99%
(S,S)-Butane-2,3-diol
(2S,3S)-Butane-2,3-diol
L-Butane-2,3-diol
[Molecular Formula]

C4H10O2
[MDL Number]

MFCD00063648
[Molecular Weight]

90.12
[MOL File]

19132-06-0.mol
Chemical PropertiesBack Directory
[Appearance]

SLIGHTLY YELLOW OILY LIQUID
[Melting point ]

20°C
[alpha ]

13 º (c=neat)
[Boiling point ]

179-182 °C (lit.)
[density ]

0.992 g/mL at 20 °C(lit.)
[refractive index ]

n20/D 1.433
[Fp ]

185 °F
[storage temp. ]

2-8°C
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Oily Liquid
[pka]

14.67±0.20(Predicted)
[color ]

Slightly yellow
[Specific Gravity]

0.987
[PH]

9-10 (500g/l, H2O, 20℃)
[explosive limit]

3.1-11.4%(V)
[Optical Rotation]

[α]20/D +13°, neat
[Water Solubility ]

soluble
[BRN ]

1718899
[Stability:]

hygroscopic
[InChI]

1S/C4H10O2/c1-3(5)4(2)6/h3-6H,1-2H3/t3-,4-/m0/s1
[InChIKey]

OWBTYPJTUOEWEK-IMJSIDKUSA-N
[SMILES]

C[C@H](O)[C@H](C)O
[LogP]

-0.655 (est)
[CAS DataBase Reference]

19132-06-0(CAS DataBase Reference)
[NIST Chemistry Reference]

2,3-Butanediol, [S-(R*,R*)]-(19132-06-0)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H227
[Precautionary statements ]

P210-P280-P370+P378-P403+P235-P501
[Hazard Codes ]

Xi
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
[RIDADR ]

NA 1993 / PGIII
[WGK Germany ]

3
[HS Code ]

29053995
[Storage Class]

10 - Combustible liquids
Raw materials And Preparation ProductsBack Directory
[Preparation Products]

Succinic acid-->CC-2SH adhesive composite used in anterior teeth-->conductive coating-composite system of acrylic copolymer and cuprous iodide
Questions And AnswerBack Directory
[Description]

2, 3-Butanediol, which is very important for a variety of chemical feedstocks and liquid fuels, can be derived from the bioconversion of natural resources1-2. It may be used in the production of antifreeze solvents, extraction solvents, butadiene, polymers, polyurethane and diacetyl and may also be used as a fuel1, 2. It can be used as a precursor in the manufacture of a range of chemical products, various plastics and pesticides, including the solvents methyl ethyl ketone (MEK), gamma-butyrolactone (GBL), and 1, 3-butadiene3. Methyl ethyl ketone can be used as a liquid fuel additive. Many other derivatives for potential uses as antifreeze agent (levo-form of 2,3 BDL), solvents, and plastic can also be prepared from 2.3-BDL. Furthermore, it can be added as a flavoring agent in food products when converted to a diacetyl by dehydrogenation2. Nowadays, it has been more and more applied of microbial fermentation for the production of 2.3-BDL2,4.
[Reference]

  1. https://www.sigmaaldrich.com/catalog/product/sial/18967?lang=en&region=US
  2. Lee, Jinwon, et al. "Biological production of 2,3-butanediol." Applied Microbiology & Biotechnology 55.1(2001):10-8.
  3. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3147483/
  4. Oliver, John W. K., et al. "Cyanobacterial conversion of carbon dioxide to 2, 3-butanediol. PNAS 110.4(2013):1249-1254.
Hazard InformationBack Directory
[Chemical Properties]

SLIGHTLY YELLOW OILY LIQUID
[Uses]

(S,S)-2,3-Butanediol is the (S,S)-isomer of 2,3-Butanediol (B690020), a naturally occurring compound found in cocoa butter.
[Definition]

ChEBI: The (S,S) diastereoisomer of butane-2,3-diol.
[General Description]

L-(+)-2,3-Butanediol is a stereoisomer of 2,3-Butanediol (2,3-BD). 2,3-BD may be used in the production of antifreeze solvents, extraction solvents, butadiene, polymers, polyurethane and diacetyl and may also be used as a fuel.
[Synthesis]

(1) 6.06 g of the ketoreductase-containing solution obtained in step 1 above was placed in a clean 250 mL single-necked flask equipped with a magnet with 20 mL of phosphate buffer salt solution at a concentration of 0.01 mol/L, and the single-necked fl

[Purification Methods]

Purify it by fractional distillation. The bis-(4-nitrobenzoate) has m 141-142o and [] (-) or (+) 52o (c 4 CHCl3). [Ghirardelli & Lucas J Am Chem Soc 79 734 1957, Rubin et al. J Am Chem Soc 74 425 1952, Neish Can J Res 27 6 1949, Neish & Ledingham Can J Res 27 694 1949, Beilstein 1 IV 2524-2525.]
Spectrum DetailBack Directory
[Spectrum Detail]

(S,S)-2,3-Butanediol(19132-06-0)MS
(S,S)-2,3-Butanediol(19132-06-0)1HNMR
(S,S)-2,3-Butanediol(19132-06-0)13CNMR
(S,S)-2,3-Butanediol(19132-06-0)IR1
(S,S)-2,3-Butanediol(19132-06-0)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

(2S,3S)-(+)-2,3-Butanediol, 99%(19132-06-0)
[Sigma Aldrich]

19132-06-0(sigmaaldrich)
[TCI AMERICA]

(S,S)-(+)-2,3-Butanediol,>97.0%(GC)(19132-06-0)
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