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Sulfur Trioxide - Triethylamine Complex - >95.0%, high purity , CAS No.761-01-3

  • ≥95%
Item Number
S161206
Grouped product items
SKUSizeAvailabilityPrice Qty
S161206-1g
1g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$15.90
S161206-5g
5g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$59.90
S161206-25g
25g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$197.90
S161206-100g
100g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$711.90
S161206-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$3,201.90

Discover Sulfur Trioxide - Triethylamine Complex by Aladdin Scientific in >95.0% for only $15.90. Available - in Ligands at Aladdin Scientific. Tags: Chemical Biology, oxidation reaction.

Basic Description

Synonyms761-01-3|N,N-diethylethanamine; sulfur trioxide|N,N-diethylethanamine;sulfur trioxide|NSC8168|Et3N.SO3|triethylamine sulphur trioxide|SCHEMBL284131|DTXSID90278539|YYHPEVZFVMVUNJ-UHFFFAOYSA-N|NSC-8168|NSC68185|MFCD00043315|NSC-68185|LS-13236|CS-0199232|FT-
Specifications & Purity>95.0%
Storage TempStore at 2-8°C,Argon charged
Shipped InWet ice
Product Description

Reactant for reagent for synthesis of: . Anticoagulant and antiplatelet persulfated glycosides or flavonoids containing an oligopolysulfated moiety . Narciclasine derivatives for use as anticancer agents . Sulfate-conjugated methylprednisolone for use as a colon-specific prodrug . Tetrasaccharide substrates of heparanase by glycosylation of disaccharides . Synthetic heparin oligosaccharide microarrays for analysis of heparin-protein interactions . Dexamethasone 21-sulfate sodium for use as a colon-specific prodrug

Names and Identifiers

IUPAC Name N,N-diethylethanamine;sulfur trioxide
INCHI InChI=1S/C6H15N.O3S/c1-4-7(5-2)6-3;1-4(2)3/h4-6H2,1-3H3;
InChi Key YYHPEVZFVMVUNJ-UHFFFAOYSA-N
Canonical SMILES CCN(CC)CC.O=S(=O)=O
Isomeric SMILES CCN(CC)CC.O=S(=O)=O
WGK Germany 3
PubChem CID 222301
Molecular Weight 181.25
Beilstein 3993170

Certificates

Certificate of Analysis(COA)

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11 results found

Lot NumberCertificate TypeDateItem
K2218666Certificate of AnalysisAug 20, 2022 S161206
K2218667Certificate of AnalysisAug 20, 2022 S161206
K2218670Certificate of AnalysisAug 20, 2022 S161206
A2211343Certificate of AnalysisDec 02, 2021 S161206
A2211354Certificate of AnalysisDec 02, 2021 S161206
A2211356Certificate of AnalysisDec 02, 2021 S161206
A2211370Certificate of AnalysisDec 02, 2021 S161206
A2211659Certificate of AnalysisDec 02, 2021 S161206
G2221322Certificate of AnalysisDec 02, 2021 S161206
G2225061Certificate of AnalysisDec 02, 2021 S161206
G2229097Certificate of AnalysisDec 02, 2021 S161206

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Chemical and Physical Properties

SolubilityChloroform (Slightly), Ethyl Acetate (Slightly)
SensitivityMoisture sensitive;heat sensitive
Melt Point(°C)93°C(lit.)

Safety and Hazards(GHS)

Pictogram(s) GHS05
Signal Danger
Hazard Statements

H314:Causes severe skin burns and eye damage

Precautionary Statements

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

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

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P260:Do not breathe dust/fume/gas/mist/vapors/spray.

P301+P330+P331:IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P363:Wash contaminated clothing before reuse.

P305+P354+P338:IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing.

P302+P361+P354:IF ON SKIN: Take off Immediately all contaminated clothing. Immediately rinse with water for several minutes.

P316:Get emergency medical help immediately.

WGK Germany 3

Related Documents

References

1. A G Fazekas,K Kókai,K Kovács.  (1967-05-01)  Effect of hexadimethrine bromide on the conversion of 4-14C-progesterone into aldosterone and corticosterone by rat adrenals..  Steroids,  ((5)): (499-506).  [PMID:6038701]
2. Christopher C Waller,Malcolm D McLeod.  (2014-10-07)  A simple method for the small scale synthesis and solid-phase extraction purification of steroid sulfates..  Steroids,  92  (74-80).  [PMID:25286236]
3. Marta Correia-da-Silva,Verónica Rocha,Cláudia Marques,Cláudia M Deus,Adriana Marques-Carvalho,Paulo J Oliveira,Andreia Palmeira,Madalena Pinto,Emília Sousa,José Manuel Sousa Lobo,Isabel Filipa Almeida.  (2018-03-29)  SULFATION PATHWAYS: Potential benefits of a sulfated resveratrol derivative for topical application..  Journal of molecular endocrinology,  61  ((2)): (M27-M39).  [PMID:29588426]
4. Vaidyanathan, et al..  (2021)  Elucidating the unusual reaction kinetics of D-glucuronyl C5-epimerase..  Glycobiology,  30  (847-858).  [PMID:32304324]
5. Alberto Sánchez-Guijo,Vinzenz Oji,Michaela F Hartmann,Hans-Christian Schuppe,Heiko Traupe,Stefan A Wudy.  (2014-12-17)  High levels of oxysterol sulfates in serum of patients with steroid sulfatase deficiency..  Journal of lipid research,  56  ((2)): (403-412).  [PMID:25502769]
6. Tarek M Bedair,Hanan M Bedair,Kyoung-Won Ko,Wooram Park,Yoon Ki Joung,Dong Keun Han.  (2019-05-28)  Persulfated flavonoids accelerated re-endothelialization and improved blood compatibility for vascular medical implants..  Colloids and surfaces. B, Biointerfaces,  181  (174-184).  [PMID:31129523]

Solution Calculators