(+/-)-1,3-Butanediol, 99%
(+/-)-1,3-Butanediol, 99%
(+/-)-1,3-Butanediol, 99%
(+/-)-1,3-Butanediol, 99%
Thermo Scientific Chemicals

(+/-)-1,3-Butanediol, 99%

CAS: 107-88-0 | C4H10O2 | 90.122 g/mol
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Catalog NumberQuantity
FSKA11684.AP500 mL
Catalog number FSKA11684.AP
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Quantity:
500 mL
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Specifications
Chemical Name or Material(±)-1,3-Butanediol
CAS107-88-0
Melting Point-50°C
Recommended StorageAmbient temperatures
Density1.005
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(±)-1,3-Butanediol acts as a co-monomer in the production of polyurethane and polyester resins. It is used as a humectant (to prevent loss of moisture) in cosmetics, especially in hair sprays and setting lotions. It is used in surfactants, inks, solvents for natural and synthetic flavorings. It is involved in the synthesis of dual peroxisome proliferator-activated gamma and delta agonists acting as euglycemic agents, which is used in the treatment of diabetes.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
(^+)-1,3-Butanediol acts as a co-monomer in the production of polyurethane and polyester resins. It is used as a humectant (to prevent loss of moisture) in cosmetics, especially in hair sprays and setting lotions. It is used in surfactants, inks, solvents for natural and synthetic flavorings. It is involved in the synthesis of dual peroxisome proliferator-activated gamma and delta agonists acting as euglycemic agents, which is used in the treatment of diabetes.

Solubility
Miscible with water.

Notes
Hygroscopic. Air and moisture sensitive. Incompatible with strong oxidizing agents, acid chlorides, chloroformates and reducing agents. Keep container tightly closed in a dry and well-ventilated place.
RUO – Research Use Only

General References:

  1. Kataoka, N.; Vangnai, A. S.; Pongtharangkul, T.; Tajima, T.; Yakushi, T.; Matsushita, K,; Kato, J. Construction of CoA-dependent 1-butanol synthetic pathway functions under aerobic conditions in Escherichia coli. J. Biotechnol. 2015, 204, 25-32.
  2. Gregory, G. L.; Ulmann, M.; Buchard, A. Synthesis of 6-membered cyclic carbonates from 1,3-diols and low CO2 pressure: a novel mild strategy to replace phosgene reagents. RSC Adv. 2015, 5, 39404-39408.