(+/-)-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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產品號碼 A11684.0D
亦稱為 A11684-0D
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10,000 mL
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化學識別
CAS107-88-0
IUPAC Namebutane-1,3-diol
Molecular FormulaC4H10O2
InChI KeyPUPZLCDOIYMWBV-UHFFFAOYNA-N
SMILESCC(O)CCO
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規格Specification Sheet規格表
Refractive Index1.4385-1.4415 @ 20?C
FormLiquid
Identification (FTIR)Conforms
Optical Rotation0.0 ± 0.2? (neat)
Appearance (Color)Clear colorless
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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.