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Diphenhydramine

CAS No.
58-73-1
Chemical Name:
Diphenhydramine
Synonyms
Benadryl;Benzhydryl;Dimedrol;DIPHENHYDRAMINE BASE;Benzhydril;Etanautine;Benzhydramine;Difenidramina;DiMenhydraMine;2-(Diphenylmethoxy)-N,N-dimethylethylamine
CBNumber:
CB6196202
Molecular Formula:
C17H21NO
Molecular Weight:
255.35
MDL Number:
MFCD00274173
MOL File:
58-73-1.mol
MSDS File:
SDS
Last updated:2024-04-03 17:07:09

Diphenhydramine Properties

Melting point 167-172°C
Boiling point bp2.0 150-165°
Density 0.9889 (rough estimate)
refractive index 1.5450 to 1.5490
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Chloroform (Slightly), Methanol (Slightly)
form Oil
pka pKa 9.1 (Uncertain)
color Oil
Merck 14,3309
BCS Class 1
CAS DataBase Reference 58-73-1(CAS DataBase Reference)
NCI Dictionary of Cancer Terms diphenhydramine
FDA UNII 8GTS82S83M
NIST Chemistry Reference Ethylamine, 2-diphenylmethoxy-n,n-dimethyl-(58-73-1)
NCI Drug Dictionary Benadryl
ATC code D04AA32,N04AB01,R06AA02,R06AA52
EPA Substance Registry System Ethanamine, 2-(diphenylmethoxy)-N,N-dimethyl- (58-73-1)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H319-H315-H302
Precautionary statements  P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P-P264-P270-P301+P312-P330-P501
RTECS  KR6825000
HS Code  2922.19.7000
Toxicity LD50 oral in rat: 390mg/kg
NFPA 704
1
2 0

Diphenhydramine price More Price(21)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical D4744 Diphenhydramine >98.0%(GC)(T) 58-73-1 5g $46 2024-03-01 Buy
TCI Chemical D4744 Diphenhydramine >98.0%(GC)(T) 58-73-1 25g $132 2024-03-01 Buy
TRC D487128 Diphenhydramine 58-73-1 10g $435 2021-12-16 Buy
Usbiological 470664 Diphenhydramine 58-73-1 1mg $453 2021-12-16 Buy
Usbiological 470663 Diphenhydramine 58-73-1 1mg $453 2021-12-16 Buy
Product number Packaging Price Buy
D4744 5g $46 Buy
D4744 25g $132 Buy
D487128 10g $435 Buy
470664 1mg $453 Buy
470663 1mg $453 Buy

Diphenhydramine Chemical Properties,Uses,Production

Description

Diphenhydramine is one of the main representatives of antihistamine drugs that block H1 receptors. Besides antihistamine activity, diphenhydramine exhibits a local anesthetic effect, relaxes smooth muscle, and has sedative and soporific action.

Originator

Benadryl,Parke Davis,US,1946

Uses

Antihistaminic.

Uses

Diphenhydramine is used for symptoms of allergies, for treating hives, hay fever, serum sickness, and other allergic illnesses, and also as a sedative and soporific drug as an independent as well as in combination with other drugs. Synonyms of this drug are dimedrol, benadryl, allergina, valdren, and many others.

Uses

Diphenhydramine also reduces muscle rigidity and general stiffness, and has a relatively minor effect on tremors.

Definition

ChEBI: Diphenhydramine is an ether that is the benzhydryl ether of 2-(dimethylamino)ethanol. It is a H1-receptor antagonist used as a antipruritic and antitussive drug. It has a role as a H1-receptor antagonist, an antiemetic, a sedative, an anti-allergic agent, a muscarinic antagonist, an antiparkinson drug, an antipruritic drug, a local anaesthetic, an antidyskinesia agent, an antitussive and a oneirogen. It is an ether and a tertiary amino compound.

Manufacturing Process

As described in US Patent 2,421,714: (a) benzhydryl
omide is first prepared as follows: 840 parts by weight of diphenylmethane is heated to 130°C with stirring. In the presence of a 200 watt electric light 6 inches from the flask, 880 parts of
omine is added slowly. Liberation of H
occurs and addition requires 1 hour and 45 minutes. The temperature is maintained at 130°C for an additional 30 minutes. A fine stream of air is blown in to remove H
and
2 while the reaction mixture cools. Benzene (180 parts) is added and the solution used immediately in (b) below.
If pure benzhydryl
omide is desired the above reaction mixture is dissolved in ether, washed with water, sodium carbonate solution and finally with water. The ether is removed, benzene added and distilled off and the benzhydryl
omide distilled in vacuo. Yield 85%.
(b) 490 parts β-dimethylaminoethanol and 530 parts of anhydrous sodium carbonate are heated to 110°C with stirring. The addition of the benzenebenzhydryl
omide mixture is then begun. The temperature is raised to 120°- 125°C. As reaction takes place carbon dioxide is evolved, the addition requires1? hours. The mixture is kept at 125°C for 5 hours additional time. After cooling, 3,000 parts of water is added and the mixture stirred until the inorganic salts are dissolved. The mixture is transferred to a large separatory funnel and 1,500 parts of ether added. The ether solution is washed several times with water and then the ether layer extracted with 1 to 4 hydrochloric acid. The acid solution is treated with 30 parts of Darco and 30 parts Filter-Cel and filtered.
The free base is liberated from the acid solution with 20% sodium hydroxide solution and taken up in ether. The ether layer is washed with water, saturated with NaCl and then shaken with solid potassium hydroxide. The ether is removed by distillation, 200 parts of benzene added and distilled off. The residue is distilled in vacuo and the fraction 150°-165°C/2 mm is collected and amounts to 433 parts. The hydrochloride salt is prepared by dissolving the free base in anhydrous ether and slowly adding an alcoholic solution of hydrogen chloride. The solid is recrystallized from absolute alcohol-ether mixture or isopropanol-ether mixture and has a MP of 161-162°C.

Therapeutic Function

Antihistaminic

Trade name

Benadryl (Parke-Davis)

Contact allergens

This antihistaminic drug with sedative properties is mainly sold over the counter. It can be used both topically (treatment of pruritis) and orally for its antiallergic, antiemetic, sedative, and anticough properties. Allergic or photoallergic contact dermatitis and fixeddrug eruption seem to be rare.

Safety Profile

Deadly human poison by an unspecified route. Poison by ingestion, intravenous, intraperitoneal, and subcutaneous routes. Experimental reproductive effects. Human systemic effects by ingestion: somnolence, alteration of operant conditioning, changes in psychophysiological tests. Human mutation data reported. When heated to decomposition it emits toxic fumes of NO,. See also ETHERS.

Synthesis

Diphenhydramine, 2-diphenylmethoxy-N,N-dimethylamine (10.2.5), is synthesized by the esterification of 2-dimethylaminoethanol with benzhydrylbromide [35¨C37].

Synthesis_58-73-1

Environmental Fate

Diphenhydramine is fairly stable in the environment although it does undergo photodegradation. Conjugates of diphenhydramine such as diphenhydramine-N-glucuronide may be converted back to the parent compound, diphenhydramine, through enzymatic cleavage during sewage treatment process. Diphenhydramine is removed poorly through wastewater treatment processes and is found in significant concentrations in aquatic organisms downstream from such plants.
Diphenhydramine has significant risk for bioaccumulation, particularly in water downstream from wastewater and sewage treatment facilities.

Solubility in water

One gram of diphenhydramine is soluble in 1 mL of water, 2 mL of ethanol, 2 mL of chloroform, or 50 mL of acetone; the compound is very slightly soluble in benzene or ether.

Toxicity evaluation

The toxicity of antihistamines is related to their anticholinergic (antimuscarinic), antihistamine, and serotonergic activation. The action of acetylcholine at the muscarinic receptors is blocked, resulting in signs and symptoms of anticholinergic poisoning. Diphenhydramine may produce direct toxicity unrelated to its anticholinergic properties including inhibition of cardiac fast sodium channels and at higher concentrations, the drug may inhibit potassium channels, which can result in QT prolongation. Diphenhydramine also blocks the reuptake of serotonin and has been reported to cause serotonin syndrome in some individuals during overdose. The action of diphenhydramine at H-1 receptors causes sedation.

108-01-0
91-01-0
58-73-1
Synthesis of Diphenhydramine from 2-Dimethylaminoethanol and Benzhydrol
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View Lastest Price from Diphenhydramine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Diphenhydramine pictures 2024-04-12 Diphenhydramine
58-73-1
US $3.00-1.00 / kg 1kg 99.9% 10 tons Shanghai Aosiris new Material Technology Co., LTD
Diphenhydramine pictures 2024-04-02 Diphenhydramine
58-73-1
US $10.00-100.00 / kg 1kg 99% 5000 Metric Ton/Month Wuhan Xinhao Biotechnology Co., Ltd
	Diphenhydramine pictures 2024-03-29 Diphenhydramine
58-73-1
US $8.00-1.00 / KG 1KG 99% g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
  • Diphenhydramine pictures
  • Diphenhydramine
    58-73-1
  • US $3.00-1.00 / kg
  • 99.9%
  • Shanghai Aosiris new Material Technology Co., LTD
  • Diphenhydramine pictures
  • Diphenhydramine
    58-73-1
  • US $10.00-100.00 / kg
  • 99%
  • Wuhan Xinhao Biotechnology Co., Ltd
Syntedril Syntodril Vena n,n-dimethyl-4,4-diphenyl-3-oxabutylamine AURORA KA-7664 DIPHENHYDRAMINE Diphenyldramine 2-(Diphenylmethoxy)N,N-dimethylethylamine 2(diphenylmethoxy)-n,n-dimethylethylamine Aleryl Alledryl Allergan B Allergeval Allergical Allergival alpha-(2-Dimethylaminoethoxy)diphenylmethane Amidryl Antistominum Antomin Automin Bagodryl Baramine Bena Benachlor Benadrin Ben-allergin Benapon Benodin Benodine Benylan Benzantine Benzhydraminum Benzhydroamina Benzhydryl2-dimethylaminoethylether beta-(Dimethylamino)ethanol diphenylmethyl ether Histaxin Hyadrine Ibiodral Medidryl Mephadryl N-(Benzhydryloksy-etylo)dwumetyloamina n,n-dimethyl-2-(diphenylmethoxy)-ethylamin N,N-Dimethyl-2-diphenylmethyloxyethylamine N-[2-(Diphenylmethoxy)ethyl]-N,N-dimethylamine Nausen Novamina O-Benzhydryl(dimethylamino)ethanol o-benzhydryldimethylaminoethanol PM 255 pm255 Probedryl Restamin Restamine Rigidil Rigidyl S 51 s51 2-benzhydryloxyethyldimethylamine