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Prolintane hydrochloride

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Name

Prolintane hydrochloride

EINECS 214-917-0
CAS No. 1211-28-5 Density N/A
PSA 3.24000 LogP 4.23350
Solubility N/A Melting Point 133-134°
Formula C15H23 N . Cl H Boiling Point 299.9°C at 760 mmHg
Molecular Weight 253.815 Flash Point 123.3°C
Transport Information N/A Appearance N/A
Safety Poison by ingestion, subcutaneous, intraperitoneal, and intravenous routes. When heated to decomposition it emits very toxic fumes of HCl and NOx. Risk Codes N/A
Molecular Structure Molecular Structure of 1211-28-5 (prolintane hydrochloride) Hazard Symbols N/A
Synonyms

Katovit;Katovit N;Katovit hydrochloride;NSC 169914;Prolintane hydrochloride;Promotil;SP 732;Vilescon;Villescon;Pyrrolidine,1-(1-benzylbutyl)-, hydrochloride (6CI);Catovitan;Pyrrolidine, 1-(a-propylphenethyl)-, hydrochloride(7CI,8CI);Pyrrolidine, 1-[1-(phenylmethyl)butyl]-, hydrochloride (9CI);1-(a-Propylphenethyl)pyrrolidinehydrochloride;1-Phenyl-2-pyrrolidinopentane hydrochloride;

 

Prolintane hydrochloride Specification

The Prolintane hydrochloride, with the CAS registry number 1211-28-5,is also known as Pyrrolidine,1-(1-(phenylmethyl)butyl)-,hydrochloride. It belongs to the product categories of Organic matters. This chemical's molecular formula is C15H24ClN and molecular weight is 253.81.Its EINECS number is 214-917-0.What's more,Its systematic name is Prolintane hydrochloride.It is Poison by ingestion, subcutaneous, intraperitoneal, and intravenous routes. When heated to decomposition it emits very toxic fumes of HCl and NOx.

The toxicity data of Prolintane hydrochloride are as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 66mg/kg (66mg/kg)   Oyo Yakuri. Pharmacometrics. Vol. 9, Pg. 601, 1975.
mouse LD50 intravenous 25mg/kg (25mg/kg)   Oyo Yakuri. Pharmacometrics. Vol. 9, Pg. 601, 1975.
mouse LD50 oral 230mg/kg (230mg/kg)   Oyo Yakuri. Pharmacometrics. Vol. 9, Pg. 601, 1975.
mouse LD50 subcutaneous 62mg/kg (62mg/kg) BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY) Arzneimittel-Forschung. Drug Research. Vol. 14, Pg. 178, 1964.
rat LD50 intraperitoneal 78mg/kg (78mg/kg)   Oyo Yakuri. Pharmacometrics. Vol. 9, Pg. 601, 1975.
rat LD50 intravenous 40mg/kg (40mg/kg)   Oyo Yakuri. Pharmacometrics. Vol. 9, Pg. 601, 1975.
rat LD50 oral 278mg/kg (278mg/kg)   Oyo Yakuri. Pharmacometrics. Vol. 9, Pg. 601, 1975.
rat LD50 subcutaneous 142mg/kg (142mg/kg)   Oyo Yakuri. Pharmacometrics. Vol. 9, Pg. 601, 1975.

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