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Isobutyl p-aminobenzoate

Isobutyl p-aminobenzoate structure

CAS No:
94-14-4
Formula:
C11H15NO2
Chemical Name:
Isobutyl p-aminobenzoate
Synonyms:
Benzoic acid,4-amino-,2-methylpropyl ester;Cycloform;Benzoic acid,p-amino-,isobutyl ester;Isobutyl p-aminobenzoate;Isobutyl Keloform;Isocaine;Isobutyl p-aminobenzoate;Isobutyl 4-aminobenzoate;Isobutylcaine;Benzamelid;Cicloforme;Cyclocaine;Cyclogesin;Isobutamben;Isobutyl p-aminobenzobenzoate;NSC 23517;Isobutambene;2-Methylpropyl 4-aminobenzoate
Categories:
Flavors and Fragrances > Synthetic Fragrances

Description

White, crystalline scales. Almost insoluble in water; soluble in alcohol, benzene and acetone.

A local anesthetic that is chemically related to BUPIVACAINE but pharmacologically related to LIDOCAINE. It is indicated for infiltration, nerve block, and epidural anesthesia. Mepivacaine is effective topically only in large doses and therefore should not be used by this route. (From AMA Drug Evaluations, 1994, p168)

Isobutyl p-aminobenzoate Basic Attributes

Molecular Weight：

193.24

Exact Mass：

193.24

EC Number：

202-308-2

UNII：

9566855ULN

NSC Number：

760439|23517

DSSTox ID：

DTXSID9023170

HScode：

2922499990

Characteristics

PSA：

52.32000

XLogP3：

2.66280

Density：

1.0945 (rough estimate)

Melting Point：

64.5 °C

Water Solubility：

0.00 M

Safety Information

RTECS Number：

DG2955000

Precautionary statement(s)：

P261, P272, P280, P302+P352, P321, P333+P313, P363, P501

Hazard Statements：

H317

GHS Classification：

|Warning|H317 (97.44%): May cause an allergic skin reaction [Warning Sensitization, Skin]|P261, P272, P280, P302+P352, P321, P333+P313, P363, and P501|Aggregated GHS information provided by 39 companies from 2 notifications to the ECHA C&L Inventory.

Drug Information

MeSH：

Drugs that block nerve conduction when applied locally to nerve tissue in appropriate concentrations. They act on any part of the nervous system and on every type of nerve fiber. In contact with a nerve trunk, these anesthetics can cause both sensory and motor paralysis in the innervated area. Their action is completely reversible. (From Gilman AG, et. al., Goodman and Gilman's The Pharmacological Basis of Therapeutics, 8th ed) Nearly all local anesthetics act by reducing the tendency of voltage-dependent sodium channels to activate. (See all compounds classified as Anesthetics, Local.)

MeSH Entry Terms：

Carbocaïne

Isobutyl p-aminobenzoate Use and Manufacturing

Uses

Sunscreen.

Manufacturing Info：

Benzoic acid, 4-amino-, 2-methylpropyl ester: INACTIVE

Computed Properties

Molecular Weight:193.24
XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:193.110278721
Monoisotopic Mass:193.110278721
Topological Polar Surface Area:52.3
Heavy Atom Count:14
Complexity:184
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Recommended Suppliers of Isobutyl p-aminobenzoate

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Trader Supplier of API & INTERMEDIATE

Isobutyl 4-Aminobenzoate

Unit Price: $100 /KG EXW

CAS No.: 94-14-4

Grade: Pharmaceutical Grade

Content: 99%

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Guide of Isobutyl p-aminobenzoate

Description
Basic Attributes
Characteristics
Safety Information
Drug Information
Use and Manufacturing
Computed Properties
Recommended Suppliers
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Isobutyl p-aminobenzoate

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