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Source: The Open Library

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1The determination of hydrazino-hydrazide groups

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“The determination of hydrazino-hydrazide groups” Metadata:

  • Title: ➤  The determination of hydrazino-hydrazide groups
  • Author:
  • Language: English
  • Number of Pages: Median: 402
  • Publisher: ➤  Elsevier Science & Technology Books - Pergamon Press - Elsevier Science & Technology
  • Publish Date:
  • Publish Location: Oxford - New York
  • Dewey Decimal Classification: 547.442
  • Library of Congress Classification: QD-0305.00000000.A7 M34 1970

“The determination of hydrazino-hydrazide groups” Subjects and Themes:

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  • First Year Published: 1970
  • Is Full Text Available: No
  • Is The Book Public: No
  • Access Status: No_ebook

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2Verband tusschen smaak en constitutie van dicarbonzuur- dihydraziden en derivaten

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“Verband tusschen smaak en constitutie van dicarbonzuur- dihydraziden en derivaten” Metadata:

  • Title: ➤  Verband tusschen smaak en constitutie van dicarbonzuur- dihydraziden en derivaten
  • Author:
  • Language: dut
  • Number of Pages: Median: 138
  • Publisher: Eduard Ijdo
  • Publish Date:
  • Publish Location: Leiden

“Verband tusschen smaak en constitutie van dicarbonzuur- dihydraziden en derivaten” Subjects and Themes:

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Access and General Info:

  • First Year Published: 1930
  • Is Full Text Available: No
  • Is The Book Public: No
  • Access Status: No_ebook

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3Peptide synthesis with o - amino acid phenylhydrazides

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“Peptide synthesis with o - amino acid phenylhydrazides” Metadata:

  • Title: ➤  Peptide synthesis with o - amino acid phenylhydrazides
  • Author:
  • Language: English
  • Number of Pages: Median: 104
  • Publish Date:

“Peptide synthesis with o - amino acid phenylhydrazides” Subjects and Themes:

Edition Identifiers:

Access and General Info:

  • First Year Published: 1967
  • Is Full Text Available: No
  • Is The Book Public: No
  • Access Status: No_ebook

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Wiki

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Hydrazide

alkylhydrazines, hydrazides are nonbasic owing to the inductive influence of the acyl, sulfonyl, or phosphoryl substituent. A common sulfonyl hydrazide is p-toluenesulfonyl

Sodium hydrazide

Sodium hydrazide is an inorganic compound with the formula NaN2H3. It is a pale yellow solid that detonates when in contact with air, water, or alcohol

Maleic hydrazide

Maleic hydrazide
Maleic hydrazide

Maleic hydrazide, often known by the brand name Fazor, is a plant growth regulator that reduces growth through preventing cell division but not cell enlargement

Phenylpiracetam hydrazide

Phenylpiracetam hydrazide
Phenylpiracetam hydrazide

Phenylpiracetam hydrazide, also known as fonturacetam hydrazide, is a racetam that is a derivative of phenylpiracetam in which the amide group is replaced

Luminol

Luminol
Luminol

Hemimellithsäure" Archived 2015-01-02 at the Wayback Machine (On the hydrazide of trimesic acid [1,3,5-benzenetricarboxylic acid] and of hemimellitic

Luminol (C8H7N3O2) is a chemical that exhibits chemiluminescence, with a blue glow, when mixed with an appropriate oxidizing agent. Luminol is a white-to-pale-yellow crystalline solid that is soluble in most polar organic solvents but insoluble in water. Forensic investigators use luminol to detect trace amounts of blood at crime scenes, as it reacts with the iron in hemoglobin. Biologists use it in cellular assays to detect copper, iron, and cyanides as well as specific proteins via western blotting. When luminol is sprayed evenly across an area, trace amounts of an activating oxidant make the luminol emit a blue glow that can be seen in a darkened room. The glow only lasts about 30 seconds but can be documented photographically. The glow is stronger in areas receiving more spray; the intensity of the glow does not indicate the amount of blood or other activator present.

P-Toluenesulfonyl hydrazide

Zhishan P.; Qiang, T.: Research progress on the synthesis and application of the sulfonyl hydrazides blowing agent in Chemistry World 56 (2015) 125–128.

Isoniazid

Isoniazid
Isoniazid

doctoral student at the German University in Prague Josef Mally researched hydrazides of pyridinecarboxylic acids. By reacting ethyl isonicotinate with hydrazine

Hydrochlorothiazide

Hydrochlorothiazide
Hydrochlorothiazide

Hydrochlorothiazide, sold under the brand name Hydrodiuril among others, is a diuretic medication used to treat hypertension and swelling due to fluid

Hydrochlorothiazide, sold under the brand name Hydrodiuril among others, is a diuretic medication used to treat hypertension and swelling due to fluid build-up. Other uses include treating diabetes insipidus and renal tubular acidosis and to decrease the risk of kidney stones in those with a high calcium level in the urine. Hydrochlorothiazide is taken by mouth and may be combined with other blood pressure medications as a single pill to increase effectiveness. Hydrochlorothiazide is a thiazide medication which inhibits reabsorption of sodium and chloride ions from the distal convoluted tubules of the kidneys, causing a natriuresis. This initially increases urine volume and lowers blood volume. It is believed to reduce peripheral vascular resistance. Potential side effects include poor kidney function, electrolyte imbalances, including low blood potassium, and, less commonly, low blood sodium, gout, high blood sugar, and feeling lightheaded with standing. Two companies, Merck & Co. and Ciba Specialty Chemicals, state they discovered the medication which became commercially available in 1959. It is on the World Health Organization's List of Essential Medicines. It is available as a generic drug and is relatively affordable. In 2023, it was the sixteenth most commonly prescribed medication in the United States, with more than 31 million prescriptions.

Hofmann rearrangement

1002/recl.19200391204. Paulsen, Hans; Stoye, Dieter (1970). "The chemistry of hydrazides". In Zabicky, Jacob (ed.). The Chemistry of Amides. The Chemistry of Functional

ATC code J04

ATC code J04 Antimycobacterials is a therapeutic subgroup of the Anatomical Therapeutic Chemical Classification System, a system of alphanumeric codes