Chemical Compounds

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4-Aminobenzonitrile was used as derivatization reagent in capillary zone electrophoretic analysis of aldoses, ketoses and uronic acid^[3]. It was used in the synthesis of methacrylic monomers containing pendant azobenzene structures^[1]and polythiophenes containing an azobenzene moiety in the side-chain^[2].

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• Formula BrC₆H₄CHO

• •  

    assay	99%
    mp	55-58 °C (lit.)

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Like many other esters, this compound undergoes the Claisen ester condensations. The advantage of using this compound is that unwanted self-condensation reactions are avoided. Like other esters, this compound undergoes bromination at the alpha position.^[2]

Diethyl malonate can be nitrosated with excess sodium nitrite in acetic acid to afford diethyl oximinomalonate, catalytic hydrogenolysis of which in ethanol over Pd/C affords diethyl aminomalonate (DEAM). DEAM can be acetylated to produce diethyl acetamidomalonate (useful in amino-acid synthesis), or can be added with 3-substituted 2,4-diketones to boiling acetic acid to afford in maximal yield variously substituted ethyl pyrrole-2-carboxylates of interest for porphyrin synthesis...

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Item Code: PCCHEM170

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Austrian chemist Heinrich Hlasiwetz (1825-1875) is remembered for his chemical analysis of phloroglucinol.

A solution of hydrochloric acid and phloroglucinol is also used for the detection of lignin (Wiesner test). A brilliant red color develops, owing to the presence of coniferaldehydegroups in the lignin.^[19] A similar test can be performed with tolonium chloride.

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1. CAS NO:61-90-5
2. FORMULA: C₆H₁₃NO₂
3. MOLAR MASS:131.17 g/mol
4. INFORMATION OF L-LEUCINE:-Leucine is one of the essential amino acids and one of three branched chain amino acids, along with isoleucine &valine. There are eight essential amino acids in total, with the others being: l-isoleucine, l-lysine, l-methionine, l-phenylalaline, l-threonine, l-tryptophan and l-valine. (l-histidine and l-arginine are often included as EAAs).¹ They cannot be made by the body, thus must be derived from the diet. L-Leucine is found in nuts, brown rice and whole wheat bread, or supplements.² There are three branched-chain amino acids (BCAAs) in the body, L-Isoleucine, L-Valine, and L-Leucine, and all of them help promote muscle recovery after exercise.
5. BENIFITS OF L-LEUCINE:BCAAs consumed before, during or after training support muscle protein synthesis, decrease protein catabolism and are very important to the use and production of glucose for energy. Leucine enhances insulin's anabolic response, and is believed to be the most important BCAA with respect to increasing protein synthesis and prevention of muscle catabolism.
6. ³¹ Essentials of Sports Nutrition and Supplements, p. 486
7. ² Macrobolic Nutrition, p. 33
8. ³ Essentials of Sports Nutrition and Supplements, p. 474 and 498 

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In 1996, the University of California's Statewide Integrated Pest Management Project reported:

Dosages were difficult to control... and as a result soaking or spraying methods are no longer used.
The current application method involves applying metam-sodium products in foam carriers (similar to shaving cream).

The U.S. Food & Drug Administration or FDA (a major operational division of the U.S. Department of Health & Human Services) mentions "dichlobenil" in a reports entitled "Herbicidal suppression of bracken and effects on forage production.

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1. INFORMATION OF N,N'-DicyclohexylcarbodiimideN,N'-Dicyclohexylcarbodiimide is an organic compound with the chemical formula C₁₃H₂₂N₂ whose primary use is to couple amino acids during artificial peptide synthesis. Under standard conditions, it exists in the form of white crystals with a heavy, sweet odor. The low melting point of this material allows it to be melted for easy handling. It is highly soluble in dichloromethane, tetrahydrofuran,acetonitrile and dimethylformamide, but insoluble in water. The compound is often abbreviated DCC.
2. REACTIONDCC is a dehydrating agent for the preparation of amides, ketones, nitriles. In these reactions, DCC hydrates to formdicyclohexylurea (DCU), a compound that is nearly insoluble in most organic solvents and insoluble in water. The majority of the DCU is thus readily removed by filtration, although the last traces can be difficult to eliminate from non-polar products. DCC can also be used to invert secondary alcohols.
3. SAFTYDCC is a potent allergen and a sensitizer, often causing skin rashes
4. CAS NO538-75-0

5. Chemical formula	C13H22N2
   Molar mass	206.33 gmol1
   Appearance	white crystalline powder
   Density	1.325 g/cm3, solid
   Melting point	34 DegreeC (93 DegreeF; 307 K)
   Boiling point	122 DegreeC (252 DegreeF; 395 K) (at 6 mmHg

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•  Formula CH₃OC₆H₄CHO

• assay	≥97%
  bp	238 °C(lit.)
  mp	34-40 °C(lit.)
  density	1.127 g/mL at 25 °C(lit.)
  Documentation	see Safety & Documentation for available documents
  Organoleptic	floral; sweet

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• Can prevent bladder stone formation
• Easy to administer (can be mixed with food)

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CERTIFICATE OF ANALYSIS
PRODUCT NAME:P-HYDROXY BENZALDEHYDE

1. CAS NO:123-08-0

2. FORMULA: C₇H₆O₂

3. _APPEARNCE: Light Yellow Crystalline Powder/White Crystalline Powder

4. MELTING POINT:114.5-117

5. DENSITY:1,129 g/cm³

^{6. INFORMATON OF P-HYDROXY BENZALDEHYDE:p-Hydroxybenzaldehyde is an important intermediate of pharmaceutical, perfume, liquid crystal. It can generate anisaldehyde when having reaction with dimethyl sulfate, and can generate hydroxy cinnamic aldehyde upon its reaction with acetaldehyde which can further undergo oxidation to obtain cinnamic acid. The direct oxidation of this product can prepare hydroxybenzoic acid; Its reduction can generate p-hydroxyphenyl rmethanol; both of them can be used as spices; pharmaceutical intermediates; raw material of liquid crystal; other kinds of organic synthesis intermediates with a wide range of applications. In addition to be used as a spice, m-hydroxybenzaldehyde can also be used as the intermediate of producing other kind of species; it can also be used as a kind of pharmaceutical raw materials for production of phenylephrine hydrochloride, epinephrine, and quinine; nickel plating; chemical analysis reagent (sugar quantitative analysis) ; photographic emulsion and fungicides.}

^{7. HOW TO USE:t's the important intermediates of pharmaceutical industry and spices. In foreign , it's also used for synthesis of bromoxynil and chloroxynil which are kind of herbicides, and also used in the manufacture of bactericide, photographic emulsifier, nickel plating luster agent, liquid crystal, etc; In the pharmaceutical field, it can be used for synthesis of amoxicillin, antibacterial synergistic agent named TMP, 3,4,5-Trimethoxybenzaldehyde???Artificial gastrodia elata, farrerol, esmololhydrochloride; In the spicery field, it can be used for synthesis of spicery,for example: vanillin, ethyl vanillin, piperonal, springaldehyde, p-anisaldehyde, raspberry ketone natural,etc.}

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1. CAS NO :-59-23-4 

2. Formula: C6H12O6 Melting Point: 168-170° C Boiling Point: 527.1° C at 760 mmHg Density: 1.58 g/cm3

   C6H12O6

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1. CAS NO:288-32-4
2. FORMULA:C₃H₄N₂
3. MOLAR MASS:68.077 g/mol
4. APPEARNCE:white or pale yellow solid
5. MELTING PONIT:89 to 91 °C
6. BOILING POINT:256 °C
7. DENSITY:1.23 g/cm³
8. INFROMATION OF IMIDAZOLE:Imidazole is an organic compound with the formula C₃N₂H₄. It is a white or colourless solid that is soluble in water, producing a mildly alkaline solution. In chemistry, it is an aromatic heterocycle, classified as a diazole, and having non-adjacent nitrogen atoms.Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C₃N₂ ring but feature varied substituents. This ring system is present in important biological building blocks, such as histidine and the related hormone histamine. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedativemidazolam.Imidazole is an organic compound with the formula C???N???H???. It is a white or colourless solid that is soluble in water, producing a mildly alkaline solution 
9. DISCRIPTION:Imidazole is useful as a buffer in the pH range of 6.2-7.8 One of the applications of imidazole is in the purification of His-tagged proteins in immobilised metal affinity chromatography(IMAC). Imidazole is used to elute tagged proteins bound to Ni ions attached to the surface of beads in the chromatography column. An excess of imidazole is passed through the column, which displaces the His-tag from nickel co-ordination, freeing the His-tagged proteins. Imidazole has become an important part of many pharmaceuticals. Synthetic imidazoles are present in many fungicides and antifungal, antiprotozoal, and antihypertensive medications. Imidazole is part of the theophylline molecule, found in tea leaves and coffee beans, which stimulates the central nervous system. It is present in the anticancer medication mercaptopurine, which combats leukemia by interfering with DNA activities. 

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C₅H₇NO₃

L-pyroglutamic acid is sold online as a dietary supplement.^[8][9]

Magnesium pidolate, the magnesium salt of pyroglutamic acid, is a mineral supplement.

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1. INFORMATION OF L-CYSTINE:L-Cystine is a non-essential amino acid. This means your body can synthesize sufficient L-cystine to meet its requirements.
3. USES AND BENIFETIS OF L-CYSTINE:Cystine along with the amino acid methionine are the amino-acids necessary for wound healing and forming of epithelial tissue. Cystine is known to stimulate the hematopoietic system and promote the formation of white and red blood cells.
4. Cystine is used as a component for parenteral and enteral nutrition. It is used as the main active ingredient for medications used to treat dermatitis. Cystine is also used in drugs that protect liver function.
5. CAS NO:56-89-3
6. Formula -C6H12N2O4S2
7. ASSAY:98.5
8. DISCRIPTION:White crystals or crystalline powder; tasteless

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Pyruvic acid (CH₃COCOOH) is the simplest of the alpha-keto acids, with a carboxylic acid and a ketone functional group. Pyruvate, the conjugate base, CH₃COCOO⁻, is a key intermediate in several metabolic pathways.

Pyruvic acid can be made from glucose through glycolysis, converted back to carbohydrates (such as glucose) via gluconeogenesis, or to fatty acids through a reaction with acetyl-CoA.^[2] It can also be used to construct the amino acid alanine and can be converted into ethanol or lactic acid via fermentation.

Pyruvic acid supplies energy to cells through the citric acid cycle (also known as the Krebs cycle) when oxygen is present (aerobic respiration), and alternatively ferments to produce lactate when oxygen is lacking

USES:The pyruvic acid derivative bromopyruvic acid is being studied for potential cancer treatment applications by researchers at Johns Hopkins University in ways that would support the Warburg hypothesis on the cause(s) of cancer.^{[citation needed]}

Pyruvate is sold as a weight-loss supplement, though evidence supporting this use is lacking. A systematic review of six trials found a statistically significant difference in body weight with pyruvate compared to placebo. However, all of the trials had methodological weaknesses and the magnitude of the effect was small. The review also identified adverse events associated with pyruvate such as diarrhea, bloating, gas, and increase in low-density lipoprotein (LDL) cholesterol. The authors concluded that there was insufficient evidence to support the use of pyruvate for weight loss.^[7]

There is also in vitro evidence in hearts that pyruvate improves metabolism by NADH production stimulation and increases cardiac function.

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1. CAS NO24424-99-5
2. FORMULAC10H18O5
3. MOLAR MASS218.25 gmol1
4. APPEARANCEcolourless solid
5. DENSITY0.95 gcm3
6. MELTING POINT22 to 24 Degree

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1. CAS NO:110-94-1
2. FORMULA:C₅H₈O₄
3. _{MOLAR MASS:}132.12 g/mol
4. _{BOILING POINT:}200 °C
5. _{INFORMATION OF GLUTARAIC ACID:} Glutaric acid is the organic compound with the formula C₃H₆(COOH)₂ . Although the related "linear" dicarboxylic acids adipic andsuccinic acids are water-soluble only to a few percent at room temperature, the water-solubility of glutaric acid is over 50%
6. SAFTY:lutaric acid may cause irritation to the skin and eyes.^[3] Acute hazards include the fact that this compound may be harmful by ingestion, inhalation or skin absorption.
7. USES:Glutaric acid itself has been used in the production of polymers such as polyester polyols, polyamides. The odd number of carbon atoms (i.e. 5) is useful in decreasing polymer elasticity

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