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Details

Stereochemistry ACHIRAL
Molecular Formula C9H9ClO
Molecular Weight 168.62
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLORINDANOL

SMILES

OC1=CC=C(Cl)C2=C1CCC2

InChI

InChIKey=ATAJVFBUUIBIEO-UHFFFAOYSA-N
InChI=1S/C9H9ClO/c10-8-4-5-9(11)7-3-1-2-6(7)8/h4-5,11H,1-3H2

HIDE SMILES / InChI

Molecular Formula C9H9ClO
Molecular Weight 168.62
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Chlorindanol is an antiseptic agent which is rapidly leathal to vegetative bacteria (Trichophyton sp., C. albicans, E. histolytica cysts and trophozoites, T. vaginalis) and seprmatozoa in vitro. It is one of two active ingredients in a spermicidal contraceptive aerosol cream (Lanettes); with the other being laureth-9.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
The biological properties of chlorindanol, a new antiseptic agent.
1959 Apr
TOXICOLOGY AND SPERMICIDAL ACTIVITY OF A NEW CONTRACEPTIVE CREAM CONTAINING CHLORINDANOL AND LAURETH 9.
1965 Mar
[Effect of chlorindanol on fungi in vitro].
1970 Apr
Patents

Sample Use Guides

A spermicidal aerosol cream marketed under the name Lanettes contains 0.1 % w/w Chlorindanol as one of two active ingredients. Instructions for use describe liberal application inside the vagina and to the penile surface.
Route of Administration: Topical
In Vitro Use Guide
The antifungal properties of chlorindanol were assesed against yeast fungal species including Candida albicans, C. tropicalis, C. parapsilosis, C. pseudotropicalis, C. stellatoidea, C. guilliermondii, C. krusei and Torulopsis glabrata. Chlorindanol was prepared in 5% propylene glycol. Chlorindanol was found to be fungicidal at a concentration of 60 - 80 microg/mL/24 hours and fungistatic at a concentration of 20 - 40 microg/mL/24 hours. Similar activities were obseved for cultures in human seerum.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:00:22 GMT 2023
Edited
by admin
on Fri Dec 15 15:00:22 GMT 2023
Record UNII
7902N03BH0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHLORINDANOL
HSDB   MI   USAN  
USAN  
Official Name English
CLORINDANOL [MART.]
Common Name English
7-Chloro-4-indanol
Systematic Name English
CLORINDANOL
INN   MART.  
INN  
Official Name English
clorindanol [INN]
Common Name English
NSC-158565
Code English
CHLORINDANOL [HSDB]
Common Name English
CHLORINDANOL [USAN]
Common Name English
CHLORINDANOL [MI]
Common Name English
1H-INDEN-4-OL, 7-CHLORO-2,3-DIHYDRO-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C28394
Created by admin on Fri Dec 15 15:00:22 GMT 2023 , Edited by admin on Fri Dec 15 15:00:22 GMT 2023
EPA PESTICIDE CODE 600003
Created by admin on Fri Dec 15 15:00:22 GMT 2023 , Edited by admin on Fri Dec 15 15:00:22 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL1449249
Created by admin on Fri Dec 15 15:00:22 GMT 2023 , Edited by admin on Fri Dec 15 15:00:22 GMT 2023
PRIMARY
CAS
145-94-8
Created by admin on Fri Dec 15 15:00:22 GMT 2023 , Edited by admin on Fri Dec 15 15:00:22 GMT 2023
PRIMARY
NSC
158565
Created by admin on Fri Dec 15 15:00:22 GMT 2023 , Edited by admin on Fri Dec 15 15:00:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID5041774
Created by admin on Fri Dec 15 15:00:22 GMT 2023 , Edited by admin on Fri Dec 15 15:00:22 GMT 2023
PRIMARY
HSDB
2157
Created by admin on Fri Dec 15 15:00:22 GMT 2023 , Edited by admin on Fri Dec 15 15:00:22 GMT 2023
PRIMARY
MERCK INDEX
m110
Created by admin on Fri Dec 15 15:00:22 GMT 2023 , Edited by admin on Fri Dec 15 15:00:22 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C77037
Created by admin on Fri Dec 15 15:00:22 GMT 2023 , Edited by admin on Fri Dec 15 15:00:22 GMT 2023
PRIMARY
SMS_ID
100000084007
Created by admin on Fri Dec 15 15:00:22 GMT 2023 , Edited by admin on Fri Dec 15 15:00:22 GMT 2023
PRIMARY
FDA UNII
7902N03BH0
Created by admin on Fri Dec 15 15:00:22 GMT 2023 , Edited by admin on Fri Dec 15 15:00:22 GMT 2023
PRIMARY
EVMPD
SUB06759MIG
Created by admin on Fri Dec 15 15:00:22 GMT 2023 , Edited by admin on Fri Dec 15 15:00:22 GMT 2023
PRIMARY
PUBCHEM
8961
Created by admin on Fri Dec 15 15:00:22 GMT 2023 , Edited by admin on Fri Dec 15 15:00:22 GMT 2023
PRIMARY
INN
1561
Created by admin on Fri Dec 15 15:00:22 GMT 2023 , Edited by admin on Fri Dec 15 15:00:22 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY