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tert-Butyl bromide - >98.0%(GC),contains 0.5% potassium carbonate as stabilizer, high purity , CAS No.507-19-7

6 Citations

COA

Grade & Purity:

≥98%(GC)
contains 0.5% potassium carbonate as stabilizer

Cas Number: 507-19-7
Molecular Weight: 137.02
Beilstein Registry Number: 1730892
EC Number: 208-065-9
MDL number: MFCD00000125
PubChem CID: 10485
PubChem SID: 504751962

In stock

Item Number

B105785

Grouped product items
SKU	Size	Availability	Price
B105785-5g	5g	2	$9.90
B105785-25g	25g	1	$27.90
B105785-100g	100g	3	$99.90
B105785-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$154.90

View related series

Haloalkane (186) Non heterocyclic block (8163)

Basic Description

Synonyms	AKOS009031116 \| HSDB 2196 \| tertbutyl bromide \| tert-Butyl bromide \| STL282745 \| STR04155 \| NSC8418 \| NSC-8418 \| BP-31078 \| FT-0611397 \| W-105932 \| EN300-21275 \| 2-Bromo-2-methylpropane, 98% \| NSC 8418 \| T-BUTYL BROMIDE [HSDB] \| tert-Butyl bromide, 98+%,
Specifications & Purity	≥98%(GC), contains 0.5% potassium carbonate as stabilizer
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Usually used to study the massive deadenylation of adenine based-nucleosides induced by halogenated alkanes under physiological conditions.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organohalogen compounds
  - Class Organobromides

Kingdom	Organic compounds
Superclass	Organohalogen compounds
Class	Organobromides
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Organobromides
Alternative Parents	Hydrocarbon derivatives Alkyl bromides
Molecular Framework	Aliphatic acyclic compounds
Substituents	Hydrocarbon derivative - Organobromide - Alkyl halide - Alkyl bromide - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as organobromides. These are compounds containing a chemical bond between a carbon atom and a bromine atom.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	504751962
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504751962
IUPAC Name	2-bromo-2-methylpropane
INCHI	InChI=1S/C4H9Br/c1-4(2,3)5/h1-3H3
InChIKey	RKSOPLXZQNSWAS-UHFFFAOYSA-N
Smiles	CC(C)(C)Br
Isomeric SMILES	CC(C)(C)Br
WGK Germany	3
RTECS	TX4150000
UN Number	2342
Packing Group	II
Molecular Weight	137.02
Beilstein	1730892
Reaxy-Rn	1730892
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1730892&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

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.

14 results found

Lot Number	Certificate Type	Date	Item
H2304354	Certificate of Analysis	May 09, 2025	B105785
H2304357	Certificate of Analysis	May 09, 2025	B105785
H2304356	Certificate of Analysis	May 09, 2025	B105785
H2304349	Certificate of Analysis	May 09, 2025	B105785
B2209316	Certificate of Analysis	Nov 06, 2023	B105785
B2209499	Certificate of Analysis	Nov 06, 2023	B105785
B2209519	Certificate of Analysis	Nov 06, 2023	B105785
F2118229	Certificate of Analysis	Mar 15, 2023	B105785
F2118226	Certificate of Analysis	Mar 15, 2023	B105785
H2304358	Certificate of Analysis	Feb 25, 2023	B105785
H2304366	Certificate of Analysis	Feb 25, 2023	B105785
H2304359	Certificate of Analysis	Feb 25, 2023	B105785
B2316353	Certificate of Analysis	Feb 18, 2023	B105785
B2209500	Certificate of Analysis	Dec 23, 2021	B105785

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Chemical and Physical Properties

Solubility	Immiscible with water.
Sensitivity	Moisture sensitive.
Refractive Index	1.428
Flash Point(°C)	18 °C
Boil Point(°C)	72.8°C
Melt Point(°C)	-16.3°C
Molecular Weight	137.020 g/mol
XLogP3	2.000
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	0
Rotatable Bond Count	0
Exact Mass	135.989 Da
Monoisotopic Mass	135.989 Da
Topological Polar Surface Area	0.000 Å²
Heavy Atom Count	5
Formal Charge	0
Complexity	25.100
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Alternative Products

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Weiqiu Wen, Jianwei Guo, Xi Zhao, Xiong Li, Hongmei Yang, Jem-Kun Chen. (2018) Synthesis of an Efficient S/N-Based Flame Retardant and Its Application in Polycarbonate. Polymers, 10 (4): (441).
2. Dong Yu Zhu, Jian Wei Guo, Jia Xing Xian, Shu Qin Fu. (2017) Novel sulfonate-containing halogen-free flame-retardants: effect of ternary and quaternary sulfonates centered on adamantane on the properties of polycarbonate composites. RSC Advances, 7 (62): (39270-39278).
3. Yang Ya, Jin Jing, Wang Jinshou, Shi Zhen, Zhang Shenghui. (2016) Kinetics of a Hydrolysis Reaction in an Oil/Water Microemulsion System Near the Critical Point. JOURNAL OF SOLUTION CHEMISTRY, 45 (5): (702-711).
4. Jinshou Wang, Jing Jin, Yanbin Tan, Zhen Shi, Shenghu Zhang. (2016) Kinetics of a hydrolysis reaction in critical surfynol465/n-butanol/ethyl acetate/water microemulsion. JOURNAL OF MOLECULAR LIQUIDS, 218 (128).
5. Li Yongqiang, Yang Siwei, Bao Wancheng, Tao Quan, Jiang Xiuyun, Li Jipeng, He Peng, Wang Gang, Qi Kai, Dong Hui, Ding Guqiao, Xie Xiaoming. (2024) Accelerated proton dissociation in an excited state induces superacidic microenvironments around graphene quantum dots. Nature Communications, 15 (1): (1-13).
6. Ting Xu, Zihan Xue, Xinhui Li, Miaomiao Zhang, Ruige Yang, Shangshang Qin, Yong Guo. (2025) Development of Membrane-Targeting Osthole Derivatives Containing Pyridinium Quaternary Ammonium Moieties with Potent Anti-Methicillin-Resistant Staphylococcus aureus Properties. JOURNAL OF MEDICINAL CHEMISTRY, 68 (7): (7459-7475).

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