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MONOCROTALINE

CAS No.
315-22-0
Chemical Name:
MONOCROTALINE
Synonyms
CROTALINE;MONOCROTALIN;A 6080;CROTALIN;NSC 28693;NCI-C56462;Bulbus Lilii;MONOCROTALINE;Monccrotalire;MONOCRATALINE
CBNumber:
CB4361934
Molecular Formula:
C16H23NO6
Molecular Weight:
325.36
MDL Number:
MFCD00084656
MOL File:
315-22-0.mol
MSDS File:
SDS
Last updated:2024-11-19 23:02:33

MONOCROTALINE Properties

Melting point 204 °C (dec.) (lit.)
alpha -54.8o (C=5 IN CHLOROFORM)
Boiling point 463.55°C (rough estimate)
Density 1.1512 (rough estimate)
refractive index 1.5500 (estimate)
storage temp. 2-8°C
solubility Soluble in DMSO (up to 50 mg/ml with warming), in Ethanol (up to 10 mg/ml with warming) or in organic solvents such as Chloroform (up to 50 mg/ml)
form Solid
pka 12.21±0.60(Predicted)
color White
Water Solubility 11.86g/L(temperature not stated)
Merck 13,6274
BRN 48732
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 1 month.
InChIKey QVCMHGGNRFRMAD-XFGHUUIASA-N
LogP -0.370 (est)
EWG's Food Scores 3
FDA UNII 73077K8HYV
Proposition 65 List Monocrotaline
IARC 2B (Vol. 10, Sup 7) 1987
EPA Substance Registry System Monocrotaline (315-22-0)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS06,GHS08
Signal word  Danger
Hazard statements  H301-H351
Precautionary statements  P201-P301+P310+P330
Hazard Codes  T
Risk Statements  25-40-35
Safety Statements  36/37/39-45
RIDADR  UN 1544 6.1/PG 3
WGK Germany  3
RTECS  QB3140000
HazardClass  6.1(b)
PackingGroup  III
HS Code  29399990
Toxicity LD50 orally in rats: 71 mg/kg (Newberne)
NFPA 704
0
2 0

MONOCROTALINE price More Price(43)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich C2401 Crotaline 315-22-0 1g $512 2024-03-01 Buy
Cayman Chemical 16666 Monocrotaline ≥98% 315-22-0 50mg $62 2024-03-01 Buy
Cayman Chemical 16666 Monocrotaline ≥98% 315-22-0 1g $419 2024-03-01 Buy
Sigma-Aldrich PHL89251 Monocrotaline phyproof? Reference Substance 315-22-0 20mg $288 2024-03-01 Buy
Sigma-Aldrich C2401 Crotaline 315-22-0 500mg $297 2024-03-01 Buy
Product number Packaging Price Buy
C2401 1g $512 Buy
16666 50mg $62 Buy
16666 1g $419 Buy
PHL89251 20mg $288 Buy
C2401 500mg $297 Buy

MONOCROTALINE Chemical Properties,Uses,Production

Description

Monocrotaline (MCT) is a toxic 11-membered macrocyclic pyrrolizidine alkaloid (PA) derived from the seeds of the Crotalaria spectabilis plant. It poisons livestock and humans through the ingestion of contaminated grains and other foods. Pyrrolizidine alkaloid is activated by cytochrome P450 to the reactive pyrrole metabolite dehydromonocrotaline (MCTP) in the liver. The alkaloid causes pulmonary artery hypertension, right ventricular hypertrophy, and pathological changes in the pulmonary vasculature.
Monocrotaline is produced for research use. It is used in rat model to investigate human pulmonary hypertension as it offers technical simplicity, reproducibility, and low cost compared with other models of pulmonary hypertension.

References

[1] Jose G. Gomez-Arroyo, Laszlo Farkas, Aysar A. Alhussaini, Daniela Farkas, Donatas Kraskauskas, Norbert F. Voelkel, Harm J. Bogaard (2012) The monocrotaline model of pulmonary hypertension in perspective, Am J Physio Lung Cell Mol Phyisol, 302, L363-L369
[2] https://pubchem.ncbi.nlm.nih.gov/compound/monocrotaline#section=Top

Description

A hepatotoxic alkaloid of the pyrrolizidine group obtained from Crotalaria retusa and C. spectabilis, the base is laevorotatory with [α]26D - 55.7° (CHCI3). It may be characterized as the hydrochloride, m.p. 184°C ldec.); [α]28D - 38.4° (H20) and the methiodide which crystallizes from MeOH with 3 moles of solvent, m.p. 205°C (dry, dec.); [α]28D + 23.4° (MeOH). Hydrolysis with boiling Ba(OHh furnishes retronecine and monocrotic acid, C7H120 3, b.p. 145-6°C/ 18 mm which is optically inactive. This acid yields a methyl ester, b.p. 94-6°Cj 18 mm, a p-bromophenacyl ester, m.p. 78°C and a 2:4-dinitrophenylhydrazone, m.p. 95-6°C. Hydrogenation in the presence of Pt02 as catalyst yields retro_x0002_necanol and monocrotalic acid, CSH120S' m.p. 181-2°C; [α]28D - 5.33° (H20) which gives a methyl ester, m.p. 79-800 C; [α]30D - 16.2° (EtOH) and a pbromophenacyl ester, m.p. 162-3°C.

Chemical Properties

White to light tan powder

Physical properties

Appearance: white prism crystal. Solubility: soluble in methanol, ethanol, and chloroform; slightly soluble in benzene, water, ether, and acetone; insoluble in petroleum ether. Melting point: 197–198 °C. Specific optical rotation: ?54.7 ° (in chloroform).

History

In 1935, W.?M. Neil and L.?L. Russoff isolated monocrotaline from Crotalaria sessiliflora L.?Monocrotaline showed anticancer activity in?vivo, especially for treating squamous cell carcinoma, cervical cancer, and leukemia. However, since many pyrrolizidine alkaloid compounds have hepatotoxicity, further development of these compounds is restricted.
China began the research of monocrotaline, as early as 1943. Crotalaria sessiliflora L. was also recorded in the 1977 edition of the Pharmacopoeia of the People’s Republic of China. But monocrotaline was reported for its liver toxicity; teratogenic, allergic reactions; and other side effects, limiting its further clinical applications. In 1992, the Ministry of Health stopped the clinical application of monocrotaline injection. Further pharmacology study is essential for monocrotaline .

Uses

antineoplastic, insect sterilant

Uses

Crotaline has been used in hydrochloric acid (HCl) and injected into experimental animals to induce-pulmonary hypertension.

Uses

A toxic pyrrolizidine alkaloid isolated from Crotalaria spp. It is used for inducing pulmonary diseases in rats.

Definition

ChEBI: Monocrotaline is a pyrrolizidine alkaloid.

Indications

This product is available in the Pharmacopoeia of the People’s Republic of China (1977).
Clinical available formulations include gel and liposome transdermal preparations. It is effective in treating skin cancer, basal cell carcinoma, acute leukemia, and cervical and penile cancer.

General Description

This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG

Biochem/physiol Actions

Crotaline induces pulmonary vascular syndrome in rats. It is considered toxic and results in hepatic cirrhosis, enlarged liver, sinusoidal obstruction syndrome and right ventricular hypertrophy.

Pharmacology

Monocrotaline is a pyrrolizidine alkaloid which has anticancer and anti-choline effects. In vitro study suggested that monocrotaline has significant cytotoxicity in human BEL-7402, KB cancer cells through inducing DNA alkylation . Monocrotaline’s toxicity is low, but its metabolites in the liver have high liver toxicity. The metabolites are highly electrophilic and can bind to enzymes, proteins, DNA, and RNA, thus causing several side effects. Monocrotaline can reduce blood pressure and inhibit cardiac contractility and heart rate and also shows mild inhibition of respiratory rate and depth.

Clinical Use

Monocrotaline injection shows well therapeutic effect for treating squamous cell carcinoma and basal cell carcinoma. In folk, the fresh pulp or dry powder of the herb has been also used for treating squamous cell carcinoma and basal cell carcinoma .

Safety Profile

Suspected carcinogen with experimental carcinogenic data. Poison by ingestion, intravenous, intraperitoneal, and subcutaneous routes. Human mutation data reported. When heated to decomposition it emits toxic fumes of NOx.

Purification Methods

Crotaline forms prisms from absolute EtOH and recrystallises also from CHCl3. UV in 96% EtOH has max 217nm (log  3.32). [Adams et al. J Am Chem Soc 74 5612 1952, Culvenor & Smith Aust J Chem 10 474 1957.] The hydrochloride has m 212-214o (from MeOH/Et2O) and [] D28 -38.4o (c 5, H2O) [Adams & Gianturco J Am Chem Soc 78 1922 1956]. The picrate has m 230-231.5o(dec) [Adams et al. J Am Chem Soc 74 5614 1952]. [Beilstein 27 III/IV 6660.]

References

Adams, Rogers., J. Amer. Chern. Soc., 61,2815 (1939)

109391-29-9
315-22-0
Synthesis of MONOCROTALINE from 1,3-Dioxolane-4-acetic acid, α,4,5-trimethyl-5-[[2-(trimethylsilyl)ethoxy]carbonyl]-, 2,3,5,7a-tetrahydro-7-(hydroxymethyl)-1H-pyrrolizin-1-yl ester, [1α[R*(4R*,5R*)],7aβ]- (9CI)
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View Lastest Price from MONOCROTALINE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Monocrotaline pictures 2024-11-19 Monocrotaline
315-22-0
US $41.00-89.00 / mg 99.59% 10g TargetMol Chemicals Inc.
Monocrotaline pictures 2023-02-24 Monocrotaline
315-22-0
US $0.00 / mg 5mg ≥98%(HPLC) 10 g Shanghai Standard Technology Co., Ltd.
Monocrotaline pictures 2023-02-13 Monocrotaline
315-22-0
US $90.00 / kg 1kg 99% 100MT Hebei baicao biology science and technology co., ltd
  • Monocrotaline pictures
  • Monocrotaline
    315-22-0
  • US $41.00-89.00 / mg
  • 99.59%
  • TargetMol Chemicals Inc.
  • Monocrotaline pictures
  • Monocrotaline
    315-22-0
  • US $0.00 / mg
  • ≥98%(HPLC)
  • Shanghai Standard Technology Co., Ltd.
  • Monocrotaline pictures
  • Monocrotaline
    315-22-0
  • US $90.00 / kg
  • 99%
  • Hebei baicao biology science and technology co., ltd
(13-alpha,14-alpha)-14,19-dihydro-12,13-dihydroxy-20-norcrotalanan-11,15-dio (13-alpha,14-alpha)-14,19-Dihydro-12,13-dihydroxy-20-norcrotalanan-11,15-dione (2,3,4-gh)pyrrolizine-2,6(3h)-dione,(4,5,8,10,12,13,13a,13b-octahydro-4,5-dihy (2,3,4-gh)pyrrolizine-2,6(3H)-dione,(4,5,8,10,12,13,13a,13b-octahydro-4,5-dihydroxy-3,4,5-trimethyl-2H-(1,6)dioxacycloundecino- 12-beta,13-beta-dihydroxy-12-alpha,13-alpha,14-alpha-trimethylcrotal-1-enine 12beta,13beta-Dihydroxy-12alpha,13alpha,14alpha-trimethylcrotal-1-enine 14,19-dihydro-12,13-dihydroxy(13-alpha,14-alpha)-20-norcrotalanan-11,15-dione 14,19-Dihydro-12,13-dihydroxy(13alpha,14alpha)-20-norcrotalanan-11,15-dione 14,19-dihydro-12,13-dihydroxy-20-norcrotolanan-11,15-dione 20-Norcrotalanan-11,15-dione, 14,19-dihydro-12,13-dihydroxy-, (13alpha,14alpha)- 20-norcrotalanan-11,15-dione,14,19-dihydro-12,13-dihydroxy-,(13-alpha,14-al MONOCROTALINE CROTALIN 20-norcrotalanan-11,15-dione,14,19-dihydro-12,13-dihydroxy-,(13alpha,14alpha) 2H-[1,6]Dioxacycloundecino[2,3,4-gh]pyrrolizine, 20-norcrotalanan-11,15-dione deriv. 4,5-Dihydroxy-3,4,5-trimethyl-4,5,8,10,12,13,13a,13b-octahydro-2H-[1,6]dioxacycloundecino[2,3,4-gh]pyrrolizine-2,6(3H)-dione 5-trimethyl-2h-(1,6)dioxacycloundecino-droxy-4 A 6080 NCI-C56462 NSC 28693 Retronecine cyclic 2,3-dihydroxy-2,3,4-trimethylglutarate Monocrotaline,99% (2,3,4-gh)pyrrolizine-2,6(3h)-dione,(4,5,8,10,12,13,1 Monocrotalinum Monccrotalire MONOCROTALIN(CROTALIN)(RG) MONOCROTOLLINE (99%) MONOCRATALINE (13R,14R)-14,19-Dihydro-12,13-dihydroxy-20-norcrotalanan-11,15-dione Monocrotoline Monocrotaline/crotaline Crotaline,Monocrotaline Bulbus Lilii Monocrotaline, >=98% 2H-[1,6]Dioxacycloundecino[2,3,4-gh]pyrrolizine-2,6(3H)-dione,4,5,8,10,12,13,13a,13b-octahydro-4,5-dihydroxy-3,4,5-trimethyl-,(3R,4R,5R,13aR,13bR)- Crotaline, 98%, from Lilium brownii F.E.Br. ex Miellez (3R,4R,5R,8a1R,13aR)-4,5-Dihydroxy-3,4,5-trimethyl-4,5,8,8a1,10,12,13,13a-octahydro-2H-[1,6]dioxacycloundecino[2,3,4-gh]pyrrolizine-2,6(3H)-dione MONOCROTALINE USP/EP/BP MONOCROTALIN CROTALINE Monocrotaline (6CI, 7CI, 8CI) Crotaline in methanol 315-22-0 C16H24NO6 Inhibitors Amines Heterocycles chemical reagent pharmaceutical intermediate phytochemical reference standards from Chinese medicinal herbs (TCM). standardized herbal extract Miscellaneous Natural Products