Borane dimethyl sulfide complex - 9.8M in Dimethylthioamidine , CAS No.13292-87-0

CAS: 13292-87-0 Cat. No.: B431899 Peso molecular: 75.97 Beilstein Registry Number: 3663489 Número EC: 236-313-6
Disponible para pedir
GRADE & PURITY 9.8M in Dimethylthioamidine
Synonyms
MCQRPQCQMGVWIQ-UHFFFAOYSA-N | Dimethyl sulphide borane | Dimethyl sulfide borane | borane methylsulphide | boron dimethyl sulfide | FT-0652013 | Borane dimethyl sulfide complex 2.0 M in THF | UNII-93TWS7F2GX | (Dimethyl sulfide)trihydroboron | (Methylthio
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25ml
B431899-25ml
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123,90US$

145,90US$
Guardar 22,00 US$ (15.08%)
4×25ml
B431899-4×25ml
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228,90US$

525,90US$
Guardar 297,00 US$ (56.47%)
500ml
B431899-500ml
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957,90US$

1.118,90US$
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Why this grade

9.8M in Dimethylthioamidine for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged 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 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Borane dimethyl sulfide complex (BMS) is a commonly used reagent and a mediator for hydroboration reaction for the preparation of organoborane compounds, which are utilized as key intermediates in organic synthesis. BMS is also employed as a reducing agent for the reduction of various functional groups such as aldehydes, ketones, epoxides, esters, and carboxylic acids to corresponding alcohols.


Application

Borane-dimethyl sulfide (BH 3 Me 2 S) can be used as a reagent: For the selective synthesis of 1,3,5-oxygenated compounds from dimethyl 3-oxoglutarate. For the conversion of ozonides to alcohols. In the CBS-catalyzed asymmetric reduction of ferrocenyl-1,3-diketones to 1,3-diols. For enantioselective reduction of ketones to chiral secondary alcohols in the presence of C 3 -symmetric tripodal hydroxyamide as a ligand. For the hydroboration reduction and other applications. With a dendrimeric supported L-pyrrolidinol in the asymmetric reduction of indanones and tetralones.


Other Notes

10.0-10.2 M as BH 3 . May contain excess methyl sulfide.

Specifications

Sinónimos
MCQRPQCQMGVWIQ-UHFFFAOYSA-N | Dimethyl sulphide borane | Dimethyl sulfide borane | borane methylsulphide | boron dimethyl sulfide | FT-0652013 | Borane dimethyl sulfide complex 2.0 M in THF | UNII-93TWS7F2GX | (Dimethyl sulfide)trihydroboron | (Methylthio
Especificaciones y pureza
9.8M in Dimethylthioamidine
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Argon charged
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores
Sonrisas canónicas[B].CSC
InChIKeyMCQRPQCQMGVWIQ-UHFFFAOYSA-N
INCHI1S/C2H6S.B/c1-3-2;/h1-2H3;
Isómeros SMILES [B].CSC
WGK Alemania 3
Peso molecular 75.97
Beilstein 3663489
Reaxy-Rn 14759666
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=14759666&ln=

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
SuperclassOrganic salts
ClaseOrganic metal salts
SubclassOrganic metalloid salts
Intermediate Tree Nodes Not available
Direct ParentOrganic metalloid salts
Alternative Parents Sulfenyl compounds  Dialkylthioethers  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Organic metalloid salt - Dialkylthioether - Sulfenyl compound - Thioether - Hydrocarbon derivative - Organosulfur compound - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as organic metalloid salts. These are organic salt compounds containing a metalloid atom in its ionic form.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

3 results found

Lot NumberCertificate TypeFechaArticulo
B2427024Certificate of AnalysisDec 12, 2025 B431899
B2427025Certificate of AnalysisDec 12, 2025 B431899
B2427026Certificate of AnalysisDec 12, 2025 B431899
Propiedades químicas y físicas
Punto de inflamación (°F)-31 °F
Punto de inflamación (°C)-35 °C
Peso molecular72.950 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass73.0283 Da
Monoisotopic Mass73.0283 Da
Topological Polar Surface Area25.300 Ų
Heavy Atom Count4
Formal Charge0
Complexity2.800
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 Count2
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Shibin Wu, Keru Song, Jianwen Wang, Siyu Huang, Fengyue Shi, Guangdong Zhao.  (2023)  Microstructure and phase evolution behavior of SiZrBC ceramic precursors synthesized via sol–gel method.  JOURNAL OF SOLID STATE CHEMISTRY,      [PMID:] [10.1016/j.jssc.2023.123910]
2. Hui-Ling Duan, Xu Deng, Jun Wang, Li Fan, Yu-Cheng Yang, Zhi-Qi Zhang.  (2020)  Ethanolamine- and amine-functionalized porous cyclodextrin polymers for efficient removal of anionic dyes from water.  EUROPEAN POLYMER JOURNAL,      [PMID:] [10.1016/j.eurpolymj.2020.109762]
3. Yuang Li, Yingli Zhu, Gangtao Luo, Pingan Chen, Mengke Qiao, Fu Chen, Xiangcheng Li.  (2025)  Fe-induced stacking faults engineering for breakthrough broadband absorption in SiBCN ceramics.  JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY,      [PMID:] [10.1016/j.jmst.2025.08.063]
4. Bijie Wang, Yujie Song, Xiao Zhang, Ke Chen, Ming Liu, Xiao Hu, Liu He, Qing Huang.  (2021)  Polymer derived SiBCN(O) ceramics with tunable element content.  CERAMICS INTERNATIONAL,      [PMID:] [10.1016/j.ceramint.2021.12.246]
5. Bijie Wang, Ke Chen, Tianhao Li, Xun Sun, Ming Liu, Lingwei Yang, Xiao (Matthew) Hu, Jian Xu, Liu He, Qing Huang, Linbin Jiang, Yujie Song.  (2021)  High-Temperature Resistant Polyborosilazanes with Tailored Structures.  Polymers,  13  (3): (467).  [PMID:33535636] [10.3390/polym13030467]
6. Chunjia Luo, Yin Wang, Xi Hu, Yaofeng Wu, Yi Wang, Min Chao, Luke Yan.  (2024)  High temperature stable amorphous SiBCN microwave absorption ceramics derived from one-pot synthesis of single-source precursors.  MATERIALS RESEARCH BULLETIN,      [PMID:] [10.1016/j.materresbull.2024.112718]
7. Xi Hu, Geqing Zhang, Haodong He, Chunjia Luo, Min Chao, Guodong Sun, Luke Yan.  (2025)  Microwave absorption ceramics pyrolyzed from poly(dimethylsilylene)diacetylene-modified hyperbranched polyborosilazane.  JOURNAL OF THE AMERICAN CERAMIC SOCIETY,      [PMID:] [10.1111/jace.20586]
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