Product Details

C4H6O2 Cutting Cycle Steroids G-Butyrolactone GBL with Safe Pass Customs

Place of Origin China
Brand Name HZ
Certification ISO 9001, GMP
Model Number GBL
Min.Order Quantity 10g
Price Negotiated
Packaging Details disguised packing
Delivery Time 3~5 days
Payment Terms Western Union, MoneyGram, T/T,Bank Transfer
Supply Ability 1000kg/month

Product Features

Clear Colorless Solvent Gamma G-Butyrolactone GBL with Safe Pass Customs

Quick detials

Product name: Butyrolactone; Gamma G*B*L
MF: C4H6O2
MW: 86.09
EINECS: 202-509-5
Chemical Properties: Clear colorless oily liquid with a pleasant odor
Specification : Magic G B L with Magic effect
Usage: Butyrolactone is one kind of important fine chemicalintermediate, simultaneously also is one kind of performance fine highboiling point solvent, ideal antioxidant, plasticizer,extracting agent, absorbent, dispersing agent, solid stain, Coagulation Reagent.
Dosage:The appropriate dose of γ-butyrolactone depends on several factors such as the users age, health, and several other conditions. At this time there is not enough scientific information to determine an appropriate range of doses for gam butyrolactone.



What is γ-Butyrolactone ?

Butyrolactone (γ-butyrolactone or ) is a hygroscopic colorless liquid with a weak characteristic odor which is soluble in water. is a common solvent and reagent in chemistry as well as being used as a flavouring, as a cleaning solvent, as a superglue remover, and as a solvent in some wet aluminium electrolytic capacitors. In humans it acts as a prodrug for, and it is used as a recreational intoxicant with effects similar to alcohol.

Butyrolactone has been found in extracts from samples of unadulterated wines.[3] This finding indicates that Butyrolactone is a naturally occurring component in some wines and may be present in similar products. The concentration detected was approximately 5 μg/mL and was easily observed using a simple extraction technique followed by GC/MS analysis. Butyrolactone can be found in cheese flavourings but typically results in a content of 0.0002% Butyrolactone in the final foodstuff.

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, Butyrolactone can become an alpha-carbon nucleophile. The related compound caprolactone can be used to make a polyester in this manner.Butyrolactone is not active in its own right; its mechanism of action stems from its identity as a prodrug of .The hypnotic effect of is enhanced by combination with alcohol. A 2003 rat study showed that Butyrolactone in combination with ethanol showed a potentiated hypnotic effect, as the sleep-timing measure was longer than both of the individual components combined

Butyrolactone is rapidly converted into by paraoxonase (lactonase) enzymes, found in the blood.[7][8] Animals which lack these enzymes exhibit no effect from Butyrolactone.[7] Butyrolactone is more lipophilic (fat soluble) than, and so is absorbed faster and has higher bioavailability. Because of these pharmacokinetic differences, Butyrolactone tends to be more potent and faster-acting than, 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.


γ-Butyrolactone Application:

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, Butyrolactone can become an alpha-carbon nucleophile. The related compound caprolactone can be used to make a polyester in this manner.

Butyrolactone is not active in its own right; its mechanism of action stems from its identity as a prodrug of .
The hypnotic effect of is enhanced by combination with alcohol. A 2003 rat study showed that Butyrolactone in combination with ethanol showed a potentiated hypnotic effect, as the sleep-timing measure was longer than both of the individual components combined

Butyrolactone is a non-toxic transparent liquid in the shape of oil. It can be mixed with water and dissolved by ethanol ether, benzene and acetone. It can dissolve many other organic and inorganic compound. Using Butyrolactone is very safe and convenient, because it is a liquid with high boiling, powerful solvency, good electrical and stability properties.Butyrolactone is an important organic synthetic raw material and a fine solvent. It is mainly used as synthetic pyrolidone series products cyclopropylamine acetyl-r-butyrolactone, besides these,Butyrolactone is also used as solvent for agricultural chemicals, polymer, dyestuff and printing. Using butyrolactone as raw material, we can produce aromatic chemicals, medicinal intermediates and rust remover.


γ-Butyrolactone Effects:

Causing relaxation.
Increasing mental clarity.
Relieving depression and stress.
Prolonging life.
Improving sexual performance and pleasure.
Reducing fat.
Improving athletic performance.
Improving sleep.
As a body-builder or muscle-builder.
As a recreational drug.

1 ) It can be used to synthesize pyrrolidone products;
2 ) It can be used as a pharmaceutical intermediate, such as Cyclopropylamine and vitamin;
3 ) It can be used as a pesticide intermediate, such as herbicide and plant growth regulator;
4 ) It can be used for alkenes, alkynes extraction agent, absorbent and dispersing agent;
5 ) It can be used to synthesize resin as an antioxidant, plasticizer, dispersing agent, fixing agent and solvent;
6 ) It can be used to synthesize fiber spinning solvent, coagulant, dyeing assistant and antistatic agent;
7 ) It can be used as a raw material of color film former, electrolyte, capacitor and ink lubricant.


How does it work?

Gam butyrolactone is converted in the body to hydroxybutyrate (G H B) which affects several nerve pathways in the brain.
As a lactone, Butyrolactone is hydrolyzed under basic conditions, for example in a sodium hydroxide solution into sodium hydroxybutyrate, the sodium salt of hydroxybutyric acid. In acidic water, a mixture of the lactone and acid forms coexist in an equilibrium. These compounds then may go on to form the polymer poly(4-hydroxybutyrate). When treated with a non-nucleophilic base, such as lithium diisopropylamide, Gam Butyrolactone undergoes deprotonation alpha to the carbonyl. The related compound caprolactone can be used to make a polyester in this manner.

A variety of catalysts promote the ring-opening polymerization of butyrolactone, poly [citation needed]. The resulting polybutyrolactone reverts to the monomer by thermal cracking. It is claimed that poly is competitive with commercial biomaterial poly(4-hydroxybutyrate), or P4HB. It is further claimed that poly is cheaper to make than P4HB, although both are bio-derived.



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