Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H27N.C8H6Cl2O3 |
| Molecular Weight | 406.387 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCCCCN.OC(=O)COC1=C(Cl)C=C(Cl)C=C1
InChI
InChIKey=GDOSCZDDZQGBAJ-UHFFFAOYSA-N
InChI=1S/C12H27N.C8H6Cl2O3/c1-2-3-4-5-6-7-8-9-10-11-12-13;9-5-1-2-7(6(10)3-5)13-4-8(11)12/h2-13H2,1H3;1-3H,4H2,(H,11,12)
| Molecular Formula | C12H27N |
| Molecular Weight | 185.3495 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C8H6Cl2O3 |
| Molecular Weight | 221.037 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:01:20 GMT 2025
by
admin
on
Mon Mar 31 22:01:20 GMT 2025
|
| Record UNII |
GH0IOA21HX
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
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Preferred Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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EPA PESTICIDE CODE |
30011
Created by
admin on Mon Mar 31 22:01:20 GMT 2025 , Edited by admin on Mon Mar 31 22:01:20 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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2,4-D-dodecylammonium
Created by
admin on Mon Mar 31 22:01:20 GMT 2025 , Edited by admin on Mon Mar 31 22:01:20 GMT 2025
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PRIMARY | |||
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GH0IOA21HX
Created by
admin on Mon Mar 31 22:01:20 GMT 2025 , Edited by admin on Mon Mar 31 22:01:20 GMT 2025
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PRIMARY | |||
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62438
Created by
admin on Mon Mar 31 22:01:20 GMT 2025 , Edited by admin on Mon Mar 31 22:01:20 GMT 2025
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PRIMARY | |||
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DTXSID5040334
Created by
admin on Mon Mar 31 22:01:20 GMT 2025 , Edited by admin on Mon Mar 31 22:01:20 GMT 2025
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PRIMARY | |||
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2212-54-6
Created by
admin on Mon Mar 31 22:01:20 GMT 2025 , Edited by admin on Mon Mar 31 22:01:20 GMT 2025
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PRIMARY | |||
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218-660-5
Created by
admin on Mon Mar 31 22:01:20 GMT 2025 , Edited by admin on Mon Mar 31 22:01:20 GMT 2025
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PRIMARY |