GBL Safe Organic Solvents Gamma Butyrolactone CAS 96-48-0 for Bodybuilding

Basic Information
Place of Origin: China
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
Appearance: Colorless Liquid MOQ: 1 L
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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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