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CAS No.: | 1211-28-5 |
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Name: | prolintane hydrochloride |
Molecular Structure: | |
Formula: | C15H23 N . Cl H |
Molecular Weight: | 253.815 |
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; |
EINECS: | 214-917-0 |
Melting Point: | 133-134° |
Boiling Point: | 299.9°C at 760 mmHg |
Flash Point: | 123.3°C |
Safety: | Poison by ingestion, subcutaneous, intraperitoneal, and intravenous routes. When heated to decomposition it emits very toxic fumes of HCl and NOx. |
PSA: | 3.24000 |
LogP: | 4.23350 |
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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 |
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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. |