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Home > Encyclopedia > Benzoylhydrazine

Benzoylhydrazine

Benzoylhydrazine structure

Benzoylhydrazine 

structure
  • CAS No:

    613-94-5

  • Formula:

    C7H8N2O

  • Chemical Name:

    Benzoylhydrazine

  • Synonyms:

    Benzoic acid,hydrazide;Benzhydrazide;Hydrazine,benzoyl-;Benzoylhydrazine;Benzoic hydrazide;Benzohydrazide;NSC 644;Benzenecarboxylic acid hydrazide;N-Benzoylhydrazine;INHd 14

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

WHITE TO BEIGE NEEDLE-LIKE CRYSTALS OR POWDER


Benzohydrazide is a carbohydrazide. It derives from a benzoic acid.

Benzoylhydrazine Basic Attributes

136.15

136.15

471797

210-363-9

LLW11ZWZ20

644

DTXSID6020149

Plates from water

29280090

Characteristics

55.1

0.2

White to beige Needle-Like Crystals or Powder

1.2±0.1 g/cm3

115 °C

267 deg C (decomposes)

139.7ºC

1.577

Sol in water and alc; slightly sol in ether, acetone, chloroform

7.8X10-5 mm Hg at 25 deg C /Estimated/

Subcutaneous-mouse LD50: 122 mg/kg; subcutaneous-rabbit LDL0: 102 mg/kg

Flammable; burning produces toxic nitrogen oxide fumes

Henry's Law constant = 9.5X10-12 atm-cu m/mol at 25 °C /Estimated/

pKa = 3.03 at 20 °C (conjugate acid)

Violent reaction with benzeneselenic acid. When heated to decomposition emits toxic fumes of NOx|Hydroxyl radical reaction rate constant = 7.3X10-12 cu cm/molec-sec at 25 °C /Estimated/

Safety Information

IRRITANT

UN 2811 6.1/PG 3

3

25-36/37/38

26-45

DH1575000

T

Ventilated, low temperature and dry; stored separately from food materials in warehouse

Reacts violently with phenylselenic acid

P261-P301 + P310-P305 + P351 + P338

H301-H315-H319-H335

SRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational exposure or environmental contamination. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations.

Violent reaction with benzeneseleninic acid.

|Danger|H301 (85.71%): Toxic if swallowed [Danger Acute toxicity, oral]|P201, P202, P261, P264, P270, P271, P280, P281, P301+P310, P302+P352, P304+P340, P305+P351+P338, P308+P313, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 49 companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

... Vinyl coated hand protection, natural or reclaimed rubber protection, rubber aprons, and plastic eye and face protection ... used when working with small quantities. Where possibility of gross splashing exists, full protective clothing made of rubber, neoprene or vinyl-coated materials should be worn. For respiratory protection in situations where recommended tolerance limits ... exceeded, respiratory protective equipment... must be used. /Hydrazine and derivatives/

Toxicity

highly toxic

Binary mixtures of the osteolathyrogens benzoic hydrazide and beta-aminopropionitrile were tested to determine the joint action for these chemicals, by evaluating induction of malformation and osteolathyrism in developing frog embryos. Exposures, starting with late-blastula stage embryos, were for 96-hr with solution renewal every 24-hr. Five treatments were examined, each chemical alone (i.e., 1:0 and 0:1 solutions) and three mixtures (i.e., 3:1, 1:1, and 1:3). Following exposure, embryos were evaluated grossly and the incidences of all types of malformations and osteolathyrogenic lesions were determined. Toxic unit analysis and isobole diagrams indicated these chemicals were concentration additive in inducing malformations and osteolathyrism. Therefore, benzoic hydrazide and beta-aminopropionitrile induce osteolathyrism, in Xenopus embryos, in a similar manner.

LD50 Mouse sc 122 mg/kg

/AQUATIC SPECIES/ Binary mixtures of the osteolathyrogens benzoic hydrazide and beta-aminopropionitrile were tested to determine the joint action for these chemicals, by evaluating induction of malformation and osteolathyrism in developing frog embryos. Exposures, starting with late-blastula stage embryos, were for 96-hr with solution renewal every 24-hr. Five treatments were examined, each chemical alone (i.e., 1:0 and 0:1 solutions) and three mixtures (i.e., 3:1, 1:1, and 1:3). Following exposure, embryos were evaluated grossly and the incidences of all types of malformations and osteolathyrogenic lesions were determined. Toxic unit analysis and isobole diagrams indicated these chemicals were concentration additive in inducing malformations and osteolathyrism. Therefore, benzoic hydrazide and beta-aminopropionitrile induce osteolathyrism, in Xenopus embryos, in a similar manner.

Biological half-lives were significantly different among the three acetylation phenotypes (analysis of variance, P < 0.05): 3.94+/-1.70 hours for slow acetylators, 2.25+/-0.37 hours for intermediate acetylators, and 1.86+/-0.67 hours for rapid acetylators. /Hydrazine/

Drug Information

Benzohydrazide yields benzoic acid in rabbit: El Masri, AM, Smith, JN, & Williams, RT, Biochem J, 68, 587 (1958). /from table/|... Benzohydrazide ... /is/ metabolized by rabbits to yield hippuric acid & hydrazine.

Basic treatment: Establish a patent airway. Suction if necessary. Watch for signs of respiratory insufficiency and assist ventilations if necessary. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for pulmonary edema and treat if necessary ... . Anticipate seizures and treat if necessary ... . For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with normal saline during transport ... . Do not use emetics. For ingestion, rinse mouth and administer 5 ml/kg up to 200 ml of water for dilution if the patient can swallow, has a strong gag reflex, and does not drool. Administer activated charcoal ... . Cover skin burns with dry, sterile dressings after decontamination ... . /Hydrazine and Related Compounds/|Advanced treatment: Consider orotracheal or nasotracheal intubation for airway control in the patient who is unconscious, has severe pulmonary edema, or is in respiratory arrest. Positive pressure ventilation techniques with a bag valve mask device may be beneficial. Monitor cardiac rhythm and treat arrhythmias if necessary ... . Start an IV with D5W /SRP: "To keep open", minimal flow rate/. Use lactated Ringer's if signs of hypovolemia are present. Consider drug therapy for pulmonary edema ... . For hypotension with signs of hypovolemia, administer fluid cautiously. Consider vasopressors for hypotension with a normal fluid volume. Watch for signs of fluid overload ... . Treat seizures with diazepam ... . Monitor for signs of hypoglycemia (decreased level of consciousness, tachycardia, pallor, dilated pupils, diaphoresis, and/or a dextrose strip or glucometer reading less than 50 mg/dl) and administer 50% dextrose if necessary. Draw blood sample before administration ... . Administer 1% solution methylene blue if patient is symptomatic with severe hypoxia, cyanosis, and cardiac compromise not responding to oxygen. ... . Use proparacaine hydrochloride to assist eye irrigation ... . /Hydrazine and Related Compounds/|Specific treatment for exposure consists of thorough washing of all exposed skin areas with soap and water, copious irrigation of the eyes, and prompt removal of the patient from the source of exposure. /Hydrazines/|After inhalation, observation for progressive respiratory distress is necessary. Chest X-ray and arterial blood gases should be monitored. Administration of oxygen, intubation, and assisted ventilation may become necessary. Pneumonia and bronchitis need to be excluded. /Hydrazines/|For more Antidote and Emergency Treatment (Complete) data for BENZHYDRAZIDE (6 total), please visit the HSDB record page.

benzhydrazide

Benzoylhydrazine Use and Manufacturing

Uses

Benzoyl Hydrazine is an acyl hydrazide as potent antioxidant.

Benzoic acid, hydrazide: ACTIVE

Computed Properties

Molecular Weight:136.15
XLogP3:0.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:136.063662883
Monoisotopic Mass:136.063662883
Topological Polar Surface Area:55.1
Heavy Atom Count:10
Complexity:119
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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