Clonazolam

Clonazolam (also known as clonitrazolam) is a benzodiazepine that has been sold online as a designer drug.

The synthesis of clonazolam was first reported in 1971 and the drug was described as the most active compound in the series tested.

Clonazolam is reputed to be highly potent, and concerns have been raised that clonazolam and flubromazolam in particular may pose comparatively higher risks than other designer benzodiazepines, due to their ability to produce strong sedation and amnesia at oral doses of as little as 0.5 mg.

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Methyldienedione

Basic Info

CAS: 5173-46-6

Customized: Customized

Suitable for: Elderly, Adult

Purity: >99%

Formula Weight: 270.37

Payment: T/T, Western Union and Money Gram

Express: EMS, DHL, FedEx, etc(Door-to-Door)

Origin: China

Powder: Yes

Certification: GMP, HSE, ISO 9001, USP, BP

Molecular Formula: C18h22o2

Appearance: White Powder

Delivery: Within 24hours After Your Payment

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Ibutamoren

Ibutamoren (INN) (developmental code names MK-677, MK-0677, L-163,191) is a non-peptidic, potent, long-acting, orally-active, and selective agonist of the ghrelin receptor and a growth hormone secretagogue, mimicking the growth hormone (GH)-stimulating action of the endogenous hormone ghrelin.

Mk-677 COA:

TEST	ACCEPTANCE CRITERLA	RESULTS
	TLC	Positive
Identification	UV spectrum	Positive
	IR spectrum	Positive
Characteristics	White to yellowish-white crystalline powder	conform
Melting point	32 ~ 37ºC	33~36ºC
Specific optical rotation	+77°~+82°	+79.3°
Loss on drying	≤0.5%	0.15%
Assay	97 ~ 103%	99.08%
Free heptanoic acid	≤0.2 %	0.10%
Related substances	≤2%	Pass
	Acetone ≤100ppm	Pass
Residual solvents(GC)	Methanol ≤100ppm	Pass
	Pyridine ≤100ppm	Pass

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Gonadotropin-releasing hormone

Gonadotropin-releasing hormone (GnRH) also known as gonadoliberin, and by various other names in its endogenous form and as gonadorelin (INN) in its pharmaceutical form, is a releasing hormone responsible for the release of follicle-stimulating hormone (FSH) and luteinizing hormone (LH) from the anterior pituitary. GnRH is a tropic peptide hormone synthesized and released from GnRH neurons within the hypothalamus. The peptide belongs to gonadotropin-releasing hormone family. It constitutes the initial step in the hypothalamic–pituitary–gonadal axis.

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Sustanon

Sustanon is a trade name owned by Organon Pharmaceuticals for oil-based injectable blends of esterized testosterone compounds.

Sustanon 250 is a blend of four esterized testosterone compounds:

30 mg testosterone propionate

60 mg testosterone phenylpropionate

60 mg testosterone isocaproate

100 mg testosterone decanoate

Sustanon 100 was similar, though with three esters. This smaller dose was usually for pediatric use.

20 mg testosterone propionate

40 mg testosterone phenylpropionate

40 mg testosterone isocaproate

Sustanon 100 has not been produced since 2009.

TEST ITEMS	SPECIFICATION	RESULTS
Description	: White or Almost White Crystalline Powder
Solubility	: Practically insoluble in water, freely soluble in acetone
	and in alcohol, soluble in fatty oils.
Identification	: IR	Positive
Assay(on dry bsis)	: 97.0~103.0%	98.57%
Specific Rotation	: +84°~+90°	+85.9°
Loss On Drying	: 0.5%max	0.31%
Related Substances	: Any impurity: 0.5%max	<0.5%
	Total: 1.0%max	<1.0%
	Disregard limit: 0.05%max	<0.05%
Conclusion	The specification conform with BP2005 standard

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Metenolone enanthate

Metenolone enanthate, or methenolone enanthate, is a dihydrotestosterone (DHT)-based anabolic-androgenic steroid (AAS). It is an ester derivative of metenolone sold commonly under the brand name Primobolan Depot (injectable). When it interacts with the aromatase enzyme it does not form any estrogens. It is used by people who are very susceptible to estrogenic side effects, having lower estrogenic properties than nandrolone. Metenolone, in form of enanthate and acetate (see metenolone acetate), is available as an injection or as an oral formulation, respectively. The injection is regarded as having a higher bioavailability. It is an enanthate ester which is quite long-acting. Because it by-passes hepatic breakdown on the first pass, it also has a higher survival rate. The tablets are in a short-lived acetate form. Metenolone is not 17-alpha-alkylated, but 1-methylated for oral bioavailability. 

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Boldenone

Boldenone (INN, BAN) (brand names Equipoise, Ganabol, Equigan, Ultragan, Boldane), also known as Δ1-testosterone, 1-dehydrotestosterone, or androsta-1,4-diene-3-one-17β-ol, is a synthetic anabolic-androgenic steroid (AAS) and the 1(2)-dehydrogenated analogue of testosterone. It is often formulated as boldenone undecylenate, the undecylenate ester.

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Betamethasone

Betamethasone is a steroid medication. It is used for a number of diseases including rheumatic disorders such as rheumatoid arthritis and systemic lupus erythematosus, skin diseases such as dermatitis and psoriasis, allergic conditions such as asthma and angioedema, preterm labor to speed the development of the baby, Crohn's disease, cancers such as leukemia, and along with fludrocortisone for adrenocortical insufficiency, among others. It can be taken by mouth, injected into a muscle, or applied as a cream.

COA:

ITEMS	SPECIFICATIONS	RESULTS
Appearance	A white to almost white,odorless, crystalline powder	Conforms
Identification	Complies with the stanard	Conforms
Loss on drying	≤0.5%	0.08 %
Residue on Ignition	≤0.3%	0.3%
Specific on rotation	+118~ +126.	+ 123.4 °
Melting point	50 ℃ ~ 60 ℃	50 ℃ ~ 60 ℃
Sulphate ash	≤0.1%	0.05%
Heavy metals	≤ 20 ppm	< 20ppm
Related substance	Total impurity ≤2.0% Single impurity ≤.0%	0.41% 0.12%
Methanol	≤ 3000 ppm	Conforms
Ethylacetate	≤ 3000 ppm	Conforms
DMF	≤ 3000 ppm	Conforms
Acetone	≤ 3000 ppm	Conforms
Dichlormethane	≤ 3000 ppm	Conforms
Assay	97.0~103.0%	100.0 %
Conclusiion	This product complied with the standard of EP 6.

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Benzocaine

Benzocaine is a local anesthetic commonly used as a topical pain reliever or in cough drops. It is the active ingredient in many over-the-counter anesthetic ointments such as products for oral ulcers. It is also combined with antipyrine to form A/B otic drops to relieve ear pain and remove earwax.

Chemical properties

Benzocaine COA：

Product Benzocaine CAS No. 94-09-7 Packing 25 kg/drum Man.date 2016-06-02 Expiry date 2018-06-01 Standard USP 36 Items Specifications Results Appearance White crystalline powder White crystalline powder Identification Consistent with the standard chart Conformed Reactive Identification Orange Red Orange Red Melting Point 88ºC ~ 92ºC 89.3ºC ~ 90.3ºC Loss on Drying ≤0.5% 0.3% Easy Carbide Comply with USP standard Conformed Residue on ignition ≤0.1% Conformed Heavy Metals ≤10ppm Conformed Assay 98% ~ 102% 101.4% Particle size 90% pass 40 mesh Conformed Conclusion Qualified

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RAD140

Description:

RAD140, from its internal nonsteroidal selective androgen receptor modulator ("SARM") discovery program, for full preclinical development as a potential therapy for the treatment of age-related muscle loss (sarcopenia) and other musculoskeletal conditions such as osteoporosis. Radius selected RAD140 from a series of promising SARMs after it demonstrated exceptional selectivity for anabolic activity in well- validated in vivo models.

Radius expects to complete formal toxicology studies that will allowed.

This makes its usage significantly safer and more effective compared to traditional prohormones and anabolic steroids.

According to the Cambridgebased pharmaceuticals company Radius, the potent, orally bioavailable and nonsteroidal RAD 140 SARM is designed to make the hormonal receptors in the tissues of the body act the same way as if they're getting a good dose of testosterone, setting off the same effects as if you're cycling with prohormones and anabolic steroids minus unwanted side effects.

Moreover, clinical studies also show that RAD 140 SARM also has a few other benefits, which we will discuss more thoroughly in a moment.

Rad-140 Oral SARMs Steroids For Massive Muscle Gain 118237-47-0 Pharma Grade Steroids

COA

Item	Specification	Result
Appearance	white powder	pass
Identificaton	The retention time of the major peak is confirm to the RS	pass
Loss on Drying	Not more than 0.5%	0.33%
Assay(HPLC)	Not less than 99.0%	99.59%
Ignition residue	Not more than 0.1%	pass
Heavy metal	Not more than 20 ppm	pass

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Enobosarm

Enobosarm, also known as ostarine, is an investigational selective androgen receptor modulator (SARM) from GTX, Inc for treatment of conditions such as muscle wasting and osteoporosis, formerly under development by Merck & Company.

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Lorcaserin

Lorcaserin, currently marketed under the trade name Belviq and previously Lorqess during development, is a weight-loss drug developed by Arena Pharmaceuticals. It has serotonergic properties and acts as an anorectic.

Medical uses

Lorcaserin is used long term for weight loss in those who are obese.

Product name	LORCASERIN
CAS NO.	616202-92-7
Synonyms	LORCASERIN;(R)-8-Chloro-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine;Apd   356;Apd356;Apd-356;Ar-10a;Unii-637E494o0z;(1R)-8-Chloro-2,3,4,5-tetrahydro-1-Methyl-1H-3-benzazepine
MF	C11H14ClN
bp	288 ºC
density	1.075
Fp	128 ºC
storage temp.	-20 ºC Freezer
Appearance:	Colorless to yellow liquid
Purity:	more than 98.0%
Usage:	Pharmaceutical intermediates

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5-Methylcytosine

5-Methylcytosine is a methylated form of the DNA base cytosine that may be involved in the regulation of gene transcription. When cytosine is methylated, the DNA maintains the same sequence, but the expression of methylated genes can be altered (the study of this is part of the field of epigenetics). 5-Methylcytosine is incorporated in the nucleoside 5-methylcytidine.

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4'-Methyl-α-pyrrolidinohexiophenone

4'-Methyl-α-pyrrolidinohexiophenone or MPHP is a stimulant compound which has been reported as a novel designer drug. It is closely related to pyrovalerone, being simply its chain-lengthened homologue. In the pyrrolidinophenone series, stimulant activity is maintained so long as the positions of the aryl, ketone and pyrrolidinyl groups are held constant, while the alkyl backbone can be varied anywhere between three and as many as seven carbons, with highest potency usually seen with the pentyl or isohexyl backbone, and a variety of substituents are tolerated on the aromatic ring.

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4'-Methyl-α-pyrrolidinobutiophenone

4'-Methyl-α-pyrrolidinobutiophenone or MPBP is a stimulant compound which has been reported as a novel designer drug. It is closely related to pyrovalerone, being simply its chain-shortened homologue.

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Dimethocaine (Larocaine)

Dimethocaine (Larocaine) is a local anesthetic with stimulant properties that some studies have shown to be half the potency of cocaine.

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Anti-ERK5

synthetic peptide corresponding to amino acids 789-802 of human ERK5.

General description

Extracellular signal-regulated kinase 5 (ERK5), also referred to as big-MAP kinase 1 or BMK1, is a protein that belongs to Mitogen-activated protein kinases family and is expressed mainly in skeletal muscle, kidney, heart and placenta. It has a critical role in different cellular processes like differentiation, proliferation and survival. Anti-ERK5 (big-MAPK, BMK1) antibody can be used to study the differential tissue expression and intracellular localization of the MAP Kinase isoform in normal and neoplastic tissues. Rabbit anti-ERK5 (big-MAPK, BMK1) antibody reacts specifically with ERK5 (97 kD) from mouse fibroblast cell extract.

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5-Methyl-MDA

5-Methyl-3,4-methylenedioxyamphetamine (5-Methyl-MDA) is an entactogen and psychedelic designer drug of the amphetamine class. It is a ring-methylated homologue of MDA and a structural isomer of MDMA.

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