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2-Mercaptobenzothiazole - 98%, high purity , CAS No.149-30-4

  • ≥98%
Item Number
M104864
Grouped product items
SKUSizeAvailabilityPrice Qty
M104864-25g
25g
In stock
$22.90
M104864-100g
100g
In stock
$12.90
M104864-250g
250g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$18.90
M104864-500g
500g
In stock
$25.90

Basic Description

Synonyms2-Mercaptobenzothiazole|149-30-4|2-Benzothiazolethiol|Benzo[d]thiazole-2(3H)-thione|Captax|Benzothiazolethiol|Benzo[d]thiazole-2-thiol|MERCAPTOBENZOTHIAZOLE|1,3-Benzothiazole-2-thiol|2(3H)-Benzothiazolethione|Dermacid|Benzothiazole-2-thiol|Sulfadene|11809
Specifications & Purity≥98%
Storage TempArgon charged
Shipped InNormal
Product Description

2-Mercaptobenzothiazole (MBT) has been used in the synthesis of MBT functionalized mesoporous silica which can be used as an adsorbent for the removal of Hg(II) from aqueous solution.

It can also be used as a:

• Reference compound in photocatalytic activity tests under UV or visible light irradiation.

• Starting material for the synthesis of conjugates of 2-MBT for antitubercular activity studies.

• Starting material for the synthesis of 4-thiazolidinones.

Associated Targets

CYP3A4 Tclin Cytochrome P450 3A4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

EHMT2 Tchem Histone-lysine N-methyltransferase EHMT2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PSMB5 Tclin Proteasome subunit beta type-5 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PSMB8 Tclin Proteasome subunit beta type-8 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RUNX1 Tbio Runt-related transcription factor 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RORC Tchem Nuclear receptor ROR-gamma 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

VDR Tclin Vitamin D3 receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC6 Tclin Histone deacetylase 6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KAT2A Tchem Histone acetyltransferase KAT2A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RXRA Tclin Retinoic acid receptor RXR-alpha 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT2B7 Tchem UDP-glucuronosyltransferase 2B7 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PDK1 Tchem [Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD(+)] 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALOX15B Tchem Arachidonate 15-lipoxygenase B 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALOX15 Tchem Arachidonate 15-lipoxygenase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AHR Tclin Aryl hydrocarbon receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALDH1A1 Tchem Retinal dehydrogenase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

THRB Tclin Thyroid hormone receptor beta 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PPARG Tclin Peroxisome proliferator-activated receptor gamma 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NFE2L2 Tchem Nuclear factor erythroid 2-related factor 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

IDO1 Tchem Indoleamine 2,3-dioxygenase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KDM4E Tchem Lysine-specific demethylase 4E 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

Pubchem Sid488191178
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488191178
IUPAC Name 3H-1,3-benzothiazole-2-thione
INCHI InChI=1S/C7H5NS2/c9-7-8-5-3-1-2-4-6(5)10-7/h1-4H,(H,8,9)
InChi Key YXIWHUQXZSMYRE-UHFFFAOYSA-N
Canonical SMILES C1=CC=C2C(=C1)NC(=S)S2
Isomeric SMILES C1=CC=C2C(=C1)NC(=S)S2
WGK Germany 2
RTECS DL6475000
Alternate CAS 118090-09-8
PubChem CID 697993
UN Number 2811
Packing Group I
Molecular Weight 167.25
Beilstein 119484
Reaxy-Rn 508810

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

12 results found

Lot NumberCertificate TypeDateItem
H2401465Certificate of AnalysisJun 17, 2024 M104864
H2408680Certificate of AnalysisJun 14, 2024 M104864
H2408681Certificate of AnalysisJun 14, 2024 M104864
H2423490Certificate of AnalysisJun 14, 2024 M104864
H2423491Certificate of AnalysisJun 14, 2024 M104864
H2423492Certificate of AnalysisJun 14, 2024 M104864
H2423493Certificate of AnalysisJun 14, 2024 M104864
H2423494Certificate of AnalysisJun 14, 2024 M104864
J2325397Certificate of AnalysisOct 13, 2023 M104864
J2325398Certificate of AnalysisOct 13, 2023 M104864
I1813063Certificate of AnalysisJul 14, 2022 M104864
B2302334Certificate of AnalysisDec 08, 2021 M104864

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Chemical and Physical Properties

SolubilitySoluble in ethanol, diethyl ether, benzene, carbon tetrachloride, alkali and alkaline solutions. Slightly soluble in acetone, naphtha and glacial acetic acid. Insoluble in water and gasoline.
SensitivityAir Sensitive;Light Sensitive
Flash Point(°F)392 °F
Flash Point(°C)243 °C
Boil Point(°C)>260℃
Melt Point(°C)178.0to183.0℃

Safety and Hazards(GHS)

Pictogram(s) GHS09,   GHS07
Signal Warning
Hazard Statements

H317:May cause an allergic skin reaction

H400:Very toxic to aquatic life

H410:Very toxic to aquatic life with long lasting effects

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P273:Avoid release to the environment.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P501:Dispose of contents/container to ...

P272:Contaminated work clothing should not be allowed out of the workplace.

P333+P313:IF SKIN irritation or rash occurs: Get medical advice/attention.

P362+P364:Take off contaminated clothing and wash it before reuse.

P391:Collect spillage.

WGK Germany 2
RTECS DL6475000
Reaxy-Rn 508810
Class 6.1
Merck Index 5868

Related Documents

References

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