O-isopropyl ethylthiocarbamate - ≥95% , CAS No.141-98-0

CAS: 141-98-0 Cat. No.: O769067 EC Number: 205-517-7 PubChem CID: 3032295
AVAILABLE TO ORDER
GRADE & PURITY ≥95%
Storage
Store at 2-8°C
Shipped In
Wet ice
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Size
Status
Price
Qty
500g
O769067-500g
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$204.90

$238.90
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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Specifications & Purity
≥95%
Storage
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥95%
Names and Identifiers
Canonical SmilesCCNC(=S)OC(C)C
IUPAC NameO-propan-2-yl N-ethylcarbamothioate
InChIKeyKIACEOHPIRTHMI-UHFFFAOYSA-N
INCHI1S/C6H13NOS/c1-4-7-6(9)8-5(2)3/h5H,4H2,1-3H3,(H,7,9)
Isomeric SMILES CCNC(=S)OC(C)C
Alternate CAS 141-98-0
PubChem CID 3032295
MeSH Entry Terms Dow Z-200;N-ethyl O-isopropyl thiocarbamate;Z 200;Z-200

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganosulfur compounds
ClassThiocarbonyl compounds
SubclassThiocarbamic acid derivatives
Intermediate Tree Nodes Not available
Direct ParentThiocarbamic acid esters
Alternative Parents Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Thiocarbamic acid ester - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as thiocarbamic acid esters. These are organic compounds containing a functional group with the general structure R1OC(=S)N(R2)R3 (R1=alkyl, aryl; R2,R3=H, alkyl, aryl).
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
Molecular Weight147.240 g/mol
XLogP31.700
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count3
Exact Mass147.072 Da
Monoisotopic Mass147.072 Da
Topological Polar Surface Area53.400 Ų
Heavy Atom Count9
Formal Charge0
Complexity93.100
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Fan Feng, Haiyang He, Dan Liu, Siqing Liu, Jianjun Fang, Shuming Wen.  (2024)  Mechanism of Cu-Pb selective flotation separation based on quercetin as a novel depressant.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2024.128505]
2. Zeen Yu, Pingfeng Fu, Lianghua Wang, Yuliang Zhang, Wei Deng.  (2025)  Microbubble catalytic ozonation of refractory organic flotation reagents with steel slag and degradation pathways.  MINERALS ENGINEERING,      [PMID:] [10.1016/j.mineng.2025.109353]
Solution Calculators
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