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BIS-TRIS propane - 98%, high purity , CAS No.64431-96-5

3 Citations

COA

Grade & Purity:

≥98%

Cas Number: 64431-96-5
Molecular Weight: 282.33
Beilstein Registry Number: 1786109
EC Number: 264-899-3
MDL number: MFCD00004689
PubChem CID: 125132
PubChem SID: 504756970

In stock

Item Number

B299299

Grouped product items
SKU	Size	Availability	Price
B299299-5g	5g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$14.90
B299299-25g	25g	3	$52.90
B299299-100g	100g	3	$149.90
B299299-500g	500g	3	$529.90

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Biochemical Assay Reagents (928)

Basic Description

Synonyms	Bis-Tris propane \| MFCD00004689 \| Q4917173 \| SY018877 \| 2-[3-(2-HYDROXY-1,1-DIHYDROXYMETHYL-ETHYLAMINO)-PROPYLAMINO]-2-HYDROXYMETHYL-PROPANE-1,3-DIOL \| BIS-TRIS propane, anhydrous, free-flowing, Redi-Dri(TM), >=99.0% \| UNII-N5YD0CS4DO \| 1,3-Bis(tris[hydro
Specifications & Purity	≥98%
Storage Temp	Argon charged
Shipped In	Normal
Product Description	useful pH range 6.3 - 9.5 pKa (25 °C) (1) 6.8, (2) 9.0 BIS-TRIS Propane is Good′s buffer. It acts as ligand and forms series of dinuclear hydroxo complexes with Lanthanides(III) in the pH range 7-9. It is useful for diagnostic assay manufacturing industry. application： BIS-TRIS Propane may be used in the following studies: As buffer to investigate the influence of anions with varying nucleophilic properties on the autoxidation of oxymyoglobin (MbO2). Purification of glucose-binding protein from membranes of Sulfolobus solfataricus. As buffer during GeO2 mineralisation.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic nitrogen compounds
  - Class Organonitrogen compounds
    - Subclass Amines
      - Level5 Alkanolamines
        Level6 1,2-aminoalcohols

Kingdom	Organic compounds
Superclass	Organic nitrogen compounds
Class	Organonitrogen compounds
Subclass	Amines
Intermediate Tree Nodes	Alkanolamines
Direct Parent	1,2-aminoalcohols
Alternative Parents	Dialkylamines Primary alcohols Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	1,2-aminoalcohol - Secondary amine - Secondary aliphatic amine - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as 1,2-aminoalcohols. These are organic compounds containing an alkyl chain with an amine group bound to the C1 atom and an alcohol group bound to the C2 atom.
External Descriptors	hexol
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	504756970
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504756970
IUPAC Name	2-[3-[[1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl]amino]propylamino]-2-(hydroxymethyl)propane-1,3-diol
INCHI	InChI=1S/C11H26N2O6/c14-4-10(5-15,6-16)12-2-1-3-13-11(7-17,8-18)9-19/h12-19H,1-9H2
InChIKey	HHKZCCWKTZRCCL-UHFFFAOYSA-N
Smiles	C(CNC(CO)(CO)CO)CNC(CO)(CO)CO
Isomeric SMILES	C(CNC(CO)(CO)CO)CNC(CO)(CO)CO
WGK Germany	3
Molecular Weight	282.33
Beilstein	1786109
Reaxy-Rn	1786109
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1786109&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
K2010200	Certificate of Analysis	Sep 05, 2024	B299299
K2303097	Certificate of Analysis	Nov 09, 2023	B299299
K2303096	Certificate of Analysis	Nov 09, 2023	B299299
K2303095	Certificate of Analysis	Nov 09, 2023	B299299
K2303158	Certificate of Analysis	Nov 07, 2023	B299299
L1906032	Certificate of Analysis	Sep 08, 2023	B299299
C2309307	Certificate of Analysis	Mar 17, 2023	B299299
C2309308	Certificate of Analysis	Mar 17, 2023	B299299
C2309310	Certificate of Analysis	Mar 16, 2023	B299299
I2217083	Certificate of Analysis	Jul 22, 2022	B299299
I2217082	Certificate of Analysis	Jul 22, 2022	B299299
A2220234	Certificate of Analysis	Jan 03, 2022	B299299
A2220244	Certificate of Analysis	Jan 03, 2022	B299299
A2212346	Certificate of Analysis	Dec 10, 2021	B299299

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Chemical and Physical Properties

Solubility	Soluble in water
Sensitivity	Moisture sensitive
Melt Point(°C)	164-165°C
Molecular Weight	282.330 g/mol
XLogP3	-4.600
Hydrogen Bond Donor Count	8
Hydrogen Bond Acceptor Count	8
Rotatable Bond Count	12
Exact Mass	282.179 Da
Monoisotopic Mass	282.179 Da
Topological Polar Surface Area	145.000 Å²
Heavy Atom Count	19
Formal Charge	0
Complexity	183.000
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

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Jie Gu, Shuyun Zheng, Xiaolong Lu, Hao Zhang, Kai Ren, Ziqiang Liu, Chao Liu, Chunrui Wu. (2024) A new strategy for solving hydrophobic membrane wetting: membrane structure design for membrane pore drying by spontaneous dehydration. JOURNAL OF MEMBRANE SCIENCE, (123664).
2. Jiandong Shen, Bijiang Zhong, Wenshui Xia, Yanshun Xu. (2024) Action of structural proteins in textural deterioration of grass carp (Ctenopharyngodon idellus) fillets during refrigerated storage. INTERNATIONAL JOURNAL OF FOOD SCIENCE AND TECHNOLOGY, 59 (4): (2659-2666).
3. Seokjoon Kim, Seungjin Lee, Seokhwan Kim, Jiye Shin, Byung Seok Cha, Eun Sung Lee, Ki Soo Park. (2024) Colorimetric detection of arsenite using Tris-mediated gold nanoparticle aggregation and chitosan lateral flow strip-based signal enhancement. SENSORS AND ACTUATORS B-CHEMICAL, 407 (135469).

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