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Home > Encyclopedia > 1,10-Phenanthroline, monohydrate

1,10-Phenanthroline, monohydrate

pharmaceutical raw materials
1,10-Phenanthroline, monohydrate structure

1,10-Phenanthroline, monohydrate 

structure
  • CAS No:

    5144-89-8

  • Formula:

    C12H8N2.H2O

  • Chemical Name:

    1,10-Phenanthroline, monohydrate

  • Synonyms:

    1,10-Phenanthroline,hydrate (1:1);1,10-Phenanthroline,monohydrate;4,5-Phenanthroline monohydrate;o-Phenanthroline monohydrate

  • Categories:

    Biochemical Engineering  >  Biochemical Reagents

Description

o-Phenanthroline monohydrate (1,10-Phenanthroline monohydrate), a metal chelator, prevents the induction of chromosomal aberrations in streptozotocin-treated cells. o-Phenanthroline monohydrate forms a red chelate with Fe2+ that absorbs maximally at 510 nm[1].


O-phenanthroline monohydrate appears as white crystalline powder or solid. Slight odor. (NTP, 1992)


O-phenanthroline monohydrate appears as white crystalline powder or solid. Slight odor. (NTP, 1992)

1,10-Phenanthroline, monohydrate Basic Attributes

198.22100

198.07900

KSX215X00E

2811

DTXSID6075302

29339990

Characteristics

35.01000

2.71870

O-phenanthroline monohydrate appears as white crystalline powder or solid. Slight odor. (NTP, 1992)

1.1

103 °C @ Solvent: Water

365.1ºC at 760 mmHg

164.8ºC

H2O: <0.01 g/100 mL at 21 ºC

Store at RT.

LD50 orally in Rabbit: 132 mg/kg

Insoluble in water.

Amines, Phosphines, and Pyridines

O-PHENANTHROLINE MONOHYDRATE is incompatible with strong oxidizers. It is also incompatible with strong acids. It forms complex compounds with ferrous ions. (NTP, 1992).

Safety Information

III

6.1

UN 2811

3

R25; R50/53

S45-S60-S61

SF8437000

T

Stable. Incompatible with iron, other heavy metals, strong oxidizing agents, strong acids.

P273-P301 + P310-P501

H301-H410

Flash point data for this chemical are not available. It is probably combustible. (NTP, 1992)

|Danger|H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]|P264, P270, P273, P301+P310, P321, P330, P391, P405, and P501|Aggregated GHS information provided by 105 companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Fires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. A water spray may also be used. (NTP, 1992)

Excerpt from ERG Guide 154 [Substances - Toxic and/or Corrosive (Non-Combustible)]: As an immediate precautionary measure, isolate spill or leak area in all directions for at least 50 meters (150 feet) for liquids and at least 25 meters (75 feet) for solids. SPILL: Increase, in the downwind direction, as necessary, the isolation distance shown above. FIRE: If tank, rail car or tank truck is involved in a fire, ISOLATE for 800 meters (1/2 mile) in all directions; also, consider initial evacuation for 800 meters (1/2 mile) in all directions. (ERG, 2016)

SMALL SPILLS AND LEAKAGE: Should a spill occur while you are handling this chemical, FIRST REMOVE ALL SOURCES OF IGNITION, then you should dampen the solid spill material with 60-70% ethanol and transfer the dampened material to a suitable container. Use absorbent paper dampened with 60-70% ethanol to pick up any remaining material. Seal the absorbent paper, and any of your clothes, which may be contaminated, in a vapor-tight plastic bag for eventual disposal. Solvent wash all contaminated surfaces with 60-70% ethanol followed by washing with a soap and water solution. Do not reenter the contaminated area until the Safety Officer (or other responsible person) has verified that the area has been properly cleaned. STORAGE PRECAUTIONS: You should store this chemical under refrigerated temperatures, and keep it away from oxidizing materials and strong acids. (NTP, 1992)

RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter. (NTP, 1992)

Drug Information

Agents that are capable of inserting themselves between the successive bases in DNA, thus kinking, uncoiling or otherwise deforming it and therefore preventing its proper functioning. They are used in the study of DNA. (See all compounds classified as Intercalating Agents.)|Chemicals that bind to and remove ions from solutions. Many chelating agents function through the formation of COORDINATION COMPLEXES with METALS. (See all compounds classified as Chelating Agents.)|Reagents with two reactive groups, usually at opposite ends of the molecule, that are capable of reacting with and thereby forming bridges between side chains of amino acids in proteins; the locations of naturally reactive areas within proteins can thereby be identified; may also be used for other macromolecules, like glycoproteins, nucleic acids, or other. (See all compounds classified as Cross-Linking Reagents.)|Drugs that inhibit cholinesterases. The neurotransmitter ACETYLCHOLINE is rapidly hydrolyzed, and thereby inactivated, by cholinesterases. When cholinesterases are inhibited, the action of endogenously released acetylcholine at cholinergic synapses is potentiated. Cholinesterase inhibitors are widely used clinically for their potentiation of cholinergic inputs to the gastrointestinal tract and urinary bladder, the eye, and skeletal muscles; they are also used for their effects on the heart and the central nervous system. (See all compounds classified as Cholinesterase Inhibitors.)|Organic chemicals that form two or more coordination links with an iron ion. Once coordination has occurred, the complex formed is called a chelate. The iron-binding porphyrin group of hemoglobin is an example of a metal chelate found in biological systems. (See all compounds classified as Iron Chelating Agents.)|Compounds which inhibit or antagonize biosynthesis or actions of proteases (ENDOPEPTIDASES). (See all compounds classified as Protease Inhibitors.)

SYMPTOMS: Symptoms of exposure to this compound may include irritation of the skin, eyes and respiratory tract. ACUTE/CHRONIC HAZARDS: This compound is harmful if swallowed. It is also harmful if inhaled or absorbed through the skin. It is an irritant of the skin, eyes and respiratory tract. When heated to decomposition it emits toxic fumes of carbon monoxide, carbon dioxide and nitrogen oxides. (NTP, 1992)

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop. SKIN: IMMEDIATELY flood affected skin with water while removing and isolating all contaminated clothing. Gently wash all affected skin areas thoroughly with soap and water. If symptoms such as redness or irritation develop, IMMEDIATELY call a physician and be prepared to transport the victim to a hospital for treatment. INHALATION: IMMEDIATELY leave the contaminated area; take deep breaths of fresh air. If symptoms (such as wheezing, coughing, shortness of breath, or burning in the mouth, throat, or chest) develop, call a physician and be prepared to transport the victim to a hospital. Provide proper respiratory protection to rescuers entering an unknown atmosphere. Whenever possible, Self-Contained Breathing Apparatus (SCBA) should be used; if not available, use a level of protection greater than or equal to that advised under Protective Clothing. INGESTION: DO NOT INDUCE VOMITING. If the victim is conscious and not convulsing, give 1 or 2 glasses of water to dilute the chemical and IMMEDIATELY call a hospital or poison control center. Be prepared to transport the victim to a hospital if advised by a physician. If the victim is convulsing or unconscious, do not give anything by mouth, ensure that the victim's airway is open and lay the victim on his/her side with the head lower than the body. DO NOT INDUCE VOMITING. IMMEDIATELY transport the victim to a hospital. (NTP, 1992)

(OP)2Cu(I)

1,10-Phenanthroline, monohydrate Use and Manufacturing

Used as a bidentate ligand in coordination chemistry.

Computed Properties

Molecular Weight:198.22
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Exact Mass:198.079312947
Monoisotopic Mass:198.079312947
Topological Polar Surface Area:26.8
Heavy Atom Count:15
Complexity:183
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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