TAPS - ≥99% , CAS No.29915-38-6

CAS: 29915-38-6 Cat. No.: T108961 Molecular Weight: 243.28 Beilstein Registry Number: 2452420 EC Number: 249-954-1 PubChem CID: 121591
AVAILABLE TO ORDER
GRADE & PURITY ≥99%
Synonyms
3-((2-Hydroxy-1,1-bis(hydroxymethyl)ethyl)amino)-1-propanesulfonic acid | 3-(Tris(hydroxymethyl)methylamino)-1-propanesulfonic acid | CHEBI:191055 | Thiosemicarbazone | 1-Propanesulfonic acid, 3-[[2-hydroxy-1,1-bis(hydroxymethyl)ethyl]amino]- | DTXSID3067
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5g
T108961-5g
3

$9.90

$14.90
Save $5.00 (33.56%)
25g
T108961-25g
2

$22.90

$34.90
Save $12.00 (34.38%)
100g
T108961-100g
3

$52.90

$79.90
Save $27.00 (33.79%)
500g
T108961-500g
3

$103.90

$155.90
Save $52.00 (33.35%)
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

TAPS is a zwitterionic buffer used in biochemistry and molecular biology. It has a useful pH range of 7.7 - 9.1. TAPS has been utilized in capillary electrophoresis of DNA and DNA-dye complexes. Dyes can be separated by planar chromatography with electroosmotic flow containing 1 mM TAPS in the mobile phase. The stability constants of metal ions with TAPS have been investigated through the use of capillary electrophoresis. TAPS has also been shown to inhibit the activity of connexin channels. The activity of various carbonic anhydrases has been studied using TAPS physiological buffer, pKa = 8.4 at 20° C.

Specifications

Synonyms
3-((2-Hydroxy-1, 1-bis(hydroxymethyl)ethyl)amino)-1-propanesulfonic acid | 3-(Tris(hydroxymethyl)methylamino)-1-propanesulfonic acid | CHEBI:191055 | Thiosemicarbazone | 1-Propanesulfonic acid, 3-[[2-hydroxy-1, 1-bis(hydroxymethyl)ethyl]amino]- | DTXSID3067
Specifications & Purity
≥99%
Storage
Room temperature
Shipped In
Normal
Purity
≥99%
Names and Identifiers
Canonical SmilesC(CNC(CO)(CO)CO)CS(=O)(=O)O
IUPAC Name3-[[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]amino]propane-1-sulfonic acid
InChIKeyYNLCVAQJIKOXER-UHFFFAOYSA-N
INCHI1S/C7H17NO6S/c9-4-7(5-10,6-11)8-2-1-3-15(12,13)14/h8-11H,1-6H2,(H,12,13,14)
Isomeric SMILES C(CNC(CO)(CO)CO)CS(=O)(=O)O
WGK Germany 3
PubChem CID 121591
Molecular Weight 243.28
Beilstein 2452420
Reaxy-Rn 2452420

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 acids and derivatives
ClassOrganic sulfonic acids and derivatives
SubclassOrganosulfonic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentOrganosulfonic acids
Alternative Parents Sulfonyls  Alkanesulfonic acids  1,2-aminoalcohols  Dialkylamines  Primary alcohols  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Organosulfonic acid - Sulfonyl - Alkanesulfonic acid - 1,2-aminoalcohol - Secondary aliphatic amine - Secondary amine - Organopnictogen compound - Organic oxygen compound - Alcohol - Primary alcohol - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Amine - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as organosulfonic acids. These are compounds containing the sulfonic acid group, which has the general structure RS(=O)2OH (R is not a hydrogen atom).
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:

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

15 results found

Lot NumberCertificate TypeDateItem
K2120544Certificate of AnalysisSep 04, 2025 T108961
K2120553Certificate of AnalysisSep 04, 2025 T108961
F2505011Certificate of AnalysisJun 17, 2025 T108961
F2505012Certificate of AnalysisJun 13, 2025 T108961
F2116225Certificate of AnalysisMar 04, 2025 T108961
F2116378Certificate of AnalysisMar 04, 2025 T108961
F2116379Certificate of AnalysisMar 04, 2025 T108961
C2526533Certificate of AnalysisJun 18, 2024 T108961
L2424586Certificate of AnalysisJun 18, 2024 T108961
D2530360Certificate of AnalysisJun 18, 2024 T108961
D2530361Certificate of AnalysisJun 18, 2024 T108961
E2530116Certificate of AnalysisSep 23, 2022 T108961
I2220589Certificate of AnalysisSep 23, 2022 T108961
I2220602Certificate of AnalysisSep 23, 2022 T108961
I2403039Certificate of AnalysisSep 23, 2022 T108961

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Chemical and Physical Properties
Flash Point(°F)>230 ℉
Flash Point(°C)>110°C
Melt Point(°C)230-235°C
Molecular Weight243.280 g/mol
XLogP3-5.400
Hydrogen Bond Donor Count5
Hydrogen Bond Acceptor Count7
Rotatable Bond Count8
Exact Mass243.078 Da
Monoisotopic Mass243.078 Da
Topological Polar Surface Area135.000 Ų
Heavy Atom Count15
Formal Charge0
Complexity247.000
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
Documents & Articles
Citations of This Product
References
1. Yuting Li, Luhan Wang, Minhua Qian, Shengda Qi, Lei Zhou, Qiaosheng Pu.  (2022)  Concise analysis of γ-hydroxybutyric acid in beverages and urine by capillary electrophoresis with capacitively coupled contactless conductivity detection using 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid as background electrolyte.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:35675730] [10.1016/j.chroma.2022.463191]
2. Liye Yang, Guangchao Pan, Piwang Zhang, Qiang Liu, Xing Liu, Yan Li, Ying Liang, Min Zhang.  (2021)  3D printed two-in-one on-capillary detector: Combining contactless conductometric and photometric detection for capillary electrophoresis.  ANALYTICA CHIMICA ACTA,      [PMID:33867034] [10.1016/j.aca.2021.338427]
3. Wang Chen, Wang Qian, Li Shuangsi, Zhang Man, Zhao Weifeng, Sun Shudong, Zhao Changsheng.  (2017)  One-pot synthesis of highly hemocompatible polyurethane/polyethersulfone composite membranes.  POLYMER BULLETIN,  74  (9): (3797-3818).  [PMID:] [10.1007/s00289-017-1922-5]
4. Rui Zhao, Xiangjian Liu, Marlene Davis Ekpo, Yongju He, Songwen Tan.  (2024)  Exploring the Cryopreservation Mechanism and Direct Removal Strategy of TAPS in Red Blood Cell Cryopreservation.  ACS Biomaterials Science & Engineering,      [PMID:38832439] [10.1021/acsbiomaterials.3c01701]
Solution Calculators
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