Place of Origin: | China |
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Brand Name: | ChineseHormone |
Certification: | GMP, ISO 9001, USP |
Model Number: | CAS 96-48-0 |
Minimum Order Quantity: | Free samples Available |
Price: | negotiated |
Packaging Details: | as your required |
Delivery Time: | 3-7 working days |
Payment Terms: | Western Union, MoneyGram, T/T, Bitcoin |
Supply Ability: | 5000 kg / month |
MW: | 86.09 | MF: | C4H6O2 |
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Appearance: | Colorless Liquid | MOQ: | 1 L |
Email: | Tonyraws810@gmail.com | Whatsapp: | 86-15871352379 |
Wickr: | Tonyraws | ||
High Light: | pharmaceutical raw material,raw materials for pharmaceutical products |
GBL Safe organic solvents Gamma Butyrolactone CAS 96-48-0 for Bodybuilding
Gamma-Butyrolactone |
|
Alias |
Gamma Butyrolactone, 1, 4- Butyrolactone, γ -Butyroladone, GBL, BLO |
Purity |
99.0% |
Registry Number: |
96-48-0 |
Einecs No: |
202-509-5 |
MF: |
C4H6O2 |
MW: |
86.09 |
Melting Point: |
-44°C |
Boiling Point: |
206°C |
Flash Point: |
99.2°C |
Ignition temperature: |
455°C |
Refractive Index: |
nd20 :1.434~1.440 |
Density |
1.12 g/mL at 25 ° C(lit. ) |
Storage temp. |
2-8° C |
Chemical Properties: |
Colourless oily liquid |
Appearance: |
Colorless clear oily liquid with acetone-like odor |
Product Categories: |
Pharmaceutical Intermediates;Heterocycles;Miscellaneous Reagents |
Lead time |
within 24 hours upon receipt of payment |
Packing: |
Galvanied iron barrel,net weight:200kg±0.05 |
Uses:
(1) GBL can be used to produce a-pyrrolidone, 1-Methyl-2-pyrrolidinone , polyvinyl pyrrolidone, and α-Acetyl-γ-butyrolactone, etc.
(2)GBL can be used as anaesthetic and tranquilizer, used to produce ciprofloxacin and interferon, as the intermediate of vitamin and rolicyprine;
(3) GBL is the intermediate of plant growth stimulator and insecticide.
(4)GBL is a good antioxidant, plasticizer, extractant, adsorbent, dispersant, fixative and curing agent; Moreover, it can also be used in battery, capacitor and development of color film.
Product Description:
GBL is a lactone. It is hydrolyzed under basic conditions, for example in a sodium hydroxide solution into sodium gamma-hydroxybutyrate, the sodium salt of gamma-hydroxybutyric acid. Under acidic conditions it forms an equilibrium mixture of both compounds.
These compounds then may go on to form a polymer. When treated with a non-nucleophilic base, like lithium diisopropylamide, GBL can become an alpha-carbon nucleophile. The related compound caprolactone can be used to make a polyester in this manner.
GBL is not active in its own right; its mechanism of action stems from its identity as a prodrug of GHB.
The hypnotic effect of GHB is enhanced by combination with alcohol. A 2003 rat study showed that GBL in combination with ethanol showed a potentiated hypnotic effect, as the sleep-timing measure was longer than both of the individual components combined
GBL is rapidly converted into GHB by paraoxonase (lactonase) enzymes, found in the blood.[7][8] Animals which lack these enzymes exhibit no effect from GBL.[7] GBL is more lipophilic (fat soluble) than GHB, and so is absorbed faster and has higher bioavailability.
Because of these pharmacokinetic differences, GBL tends to be more potent and faster-acting than GHB, but has a shorter duration; whereas the related compound 1,4-butanediol (1,4-B) tends to be slightly less potent, slower to take effect but longer-acting than GHB.
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