1-MONONITROGLYCERIN

Suppliers

Names

[ CAS No. ]:
624-43-1

[ Name ]:
1-MONONITROGLYCERIN

[Synonym ]:
1,2,3-Propanetriol,1-nitrate
Glycerol-1-nitrate
Glycerol-1-nitrat
glyceryl 1-mononitrate
Glycerol 1-mononitrate
glycerol nitrate
propylene glycol 1-nitrate
Glycerol-1-mononitrat
1-Mononitroglycerin
1-Mononitroglycerol

Chemical & Physical Properties

[ Molecular Formula ]:
C3H7NO5

[ Molecular Weight ]:
137.09100

[ Exact Mass ]:
137.03200

[ PSA ]:
95.51000

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
MB0200000
CHEMICAL NAME :
Glycerol, 1-nitrate
CAS REGISTRY NUMBER :
624-43-1
BEILSTEIN REFERENCE NO. :
1761580
LAST UPDATED :
199612
DATA ITEMS CITED :
6
MOLECULAR FORMULA :
C3-H7-N-O5

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
339 mg/kg
TOXIC EFFECTS :
Behavioral - ataxia Lungs, Thorax, or Respiration - cyanosis Lungs, Thorax, or Respiration - respiratory depression
REFERENCE :
NTIS** National Technical Information Service. (Springfield, VA 22161) Formerly U.S. Clearinghouse for Scientific & Technical Information. Volume(issue)/page/year: AD-B011-150
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
580 mg/kg
TOXIC EFFECTS :
Behavioral - tremor Behavioral - convulsions or effect on seizure threshold Lungs, Thorax, or Respiration - cyanosis
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 36,814,1986
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
1433 mg/kg
TOXIC EFFECTS :
Behavioral - ataxia Lungs, Thorax, or Respiration - cyanosis Lungs, Thorax, or Respiration - respiratory depression
REFERENCE :
NTIS** National Technical Information Service. (Springfield, VA 22161) Formerly U.S. Clearinghouse for Scientific & Technical Information. Volume(issue)/page/year: AD-B011-150
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
3160 mg/kg
TOXIC EFFECTS :
Behavioral - tremor Behavioral - convulsions or effect on seizure threshold Lungs, Thorax, or Respiration - cyanosis
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 36,814,1986
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Mammal - dog
DOSE/DURATION :
>1 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 36,814,1986
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rabbit
DOSE/DURATION :
2 gm/kg
TOXIC EFFECTS :
Behavioral - tremor Behavioral - convulsions or effect on seizure threshold Lungs, Thorax, or Respiration - cyanosis
REFERENCE :
ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 36,814,1986

Safety Information

[ Symbol ]:

GHS02, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H225-H302 + H312 + H332-H319

[ Precautionary Statements ]:
P210-P261-P302 + P352 + P312-P304 + P340 + P312-P337 + P313-P403 + P235

[ RIDADR ]:
UN 1648 3 / PGII

Synthetic Route

Precursor & DownStream

Precursor

  • Glycerol
  • 3-BROMO-1,2-PROPANEDIOL
  • Glycidol
  • ALLYLNITRATE
  • Nitroglycerin
  • 1,3-DINITROGLYCERIN
  • 1,2-DINITROGLYCERIN
  • nitric acid
  • 1,4-Dioxane
  • 2,2,4-Trimethylpentane

DownStream

  • Glycerol
  • 1,3-DINITROGLYCERIN

Articles

Studies on the biphasic relaxant curve of glyceryl trinitrate in rat aorta: role of GTN metabolites.

Clin. Exp. Pharmacol. Physiol. 16(11) , 829-35, (1989)

1. The present study has examined the possibility that one or more metabolites of glyceryl trinitrate (GTN) (i.e. glyceryl-1,2- and -1,3-dinitrate and glyceryl-1- and -2-mononitrate) may be responsibl...

Guanylate cyclase activation by organic nitrates is not mediated via nitrite.

J. Mol. Cell. Cardiol. 20(5) , 389-96, (1988)

Nitrovasodilators relax vascular smooth muscle by stimulating guanylate cyclase. Ignarro et al. (1981) proposed a mechanistic scheme according to which organic nitrates release nitrite in the presence...

[Comparative pharmacology of glycerol-1-nitrate and glyceryl trinitrate in various species].

Arzneimittelforschung 36(5) , 814-21, (1986)

The present studies yield that all 4 metabolites of glyceryl trinitrate (Nitro Mack, GTN) cause the same typical pharmacological effects as the parent substance. Continuous infusion of 4 mg/kg/min of ...


More Articles


Related Compounds

  • 1-Mononitroglycerin
  • 1-[2-(2-fluorobenzoyl)pyrrol-1-yl]propan-2-yl-dimethylazanium,chloride
  • 1-[2-(2-methoxybenzoyl)pyrrol-1-yl]propan-2-yl-dimethylazanium,chloride
  • 1-methyl-3-[3-[[methyl-[(4-nitrophenyl)methyl]carbamoyl]amino]phenyl]-1-[(4-nitrophenyl)methyl]urea
  • 1-(2-methoxyphenyl)-4-(2-phenylethyl)piperazine
  • 1-(3-Chlorophenyl)-4-propylpiperazine
  • (3S,5S)-5-(acetamidomethyl)tetrahydrofuran-3-carboxylic acid
  • (2R)-1-allyloxycarbonyl-2-methyl-pyrrolidine-2-carboxylic acid
  • 2-[(1R,3S)-3-[(2,2,2-trifluoroacetyl)amino]cyclopentyl]acetic acid
  • 2,2,4-trimethyl-3-[(2,2,2-trifluoroacetyl)amino]pentanoic acid
  • 2-(7-acetyl-7-azabicyclo[2.2.1]heptan-1-yl)acetic acid
  • benzyl N-[(4-bromoisothiazol-5-yl)methyl]carbamate
  • 3-allyl-1-(2,2,2-trifluoroacetyl)azetidine-3-carboxylic acid
  • 1-acetyl-4,4-difluoro-piperidine-3-carboxylic acid
  • ethyl 2-amino-2-(3,3-dimethylcyclobutyl)acetate
  • (1R,5S)-5-[(2,2,2-trifluoroacetyl)amino]cyclohex-3-ene-1-carboxylic acid
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.