Ammonium formate solution - UltraBio™, Ultra pure, 10 M in H2O , CAS No.540-69-2

CAS: 540-69-2 Cat. No.: A432862 분자식: CH5NO2 분자량: 63.06 Beilstein Registry Number: 3625095 EC 번호: 208-753-9
주문 가능
등급 & 순도 UltraBio™ ? UltraBio™ — Aladdin's line for molecular-biology applications. Use for nuclease-free, high-consistency reagents across molecular workflows. Ultra pure ? Ultra-pure grade with very low impurity content across the board. Use for trace analysis, electronics, or processes intolerant of contamination. 10 M in H2O
Synonyms
HC(O)ONH4 | AMMONIUM FORMATE | ammonium for-mate | ammonium formate- | Ammonium formate-d5 | Ammoniumformiate | Ammonium-formiate | D78097 | 3801F9644E | amonium formate | EINECS 208-753-9 | Q420466 | CH5NO2 | annmonium formate | mono-ammonium formate sal
Storage
Room temperature
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가격
수량
100ml
A432862-100ml
2 재고 있음
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US$189.90

US$222.90
저장 US$33.00 (14.80%)
500ml
A432862-500ml
주문제작 · 8~12주

US$861.90

US$1,005.90
저장 US$144.00 (14.32%)
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개요

Ammonium formate is readily available, stable and nontoxic in nature. It can be used in conjugation with palladium on carbon (Pd-C) or Raney-nickel catalysts.


Application

Ammonium formate has been used as a constituent in pre-mixed eluents for forming gradient during quantification of diuron by liquid chromatography-mass spectrometry (LC-MS).

사양

동의어
HC(O)ONH4 | AMMONIUM FORMATE | ammonium for-mate | ammonium formate- | Ammonium formate-d5 | Ammoniumformiate | Ammonium-formiate | D78097 | 3801F9644E | amonium formate | EINECS 208-753-9 | Q420466 | CH5NO2 | annmonium formate | mono-ammonium formate sal
사양 및 순도
UltraBio™, Ultra pure, 10 M in H2O
보관 조건
Room temperature
등급
Ultra pure, UltraBio™
이름과 식별자
Pubchem Sid
정식 스마일
C(=O)[O-].[NH4+]
IUPAC Name
azanium;formate
InChIKey
VZTDIZULWFCMLS-UHFFFAOYSA-N
INCHI
1S/CH2O2.H3N/c2-1-3;/h1H,(H,2,3);1H3
이성체 SMILES
C(=O)[O-].[NH4+]
WGK 독일
1
분자량
63.06
Beilstein
3625095
Reaxy-Rn
3625095
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3625095&ln=

고급 데이터

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
분류Carboxylic acids and derivatives
SubclassCarboxylic acids
Intermediate Tree Nodes Not available
Direct ParentCarboxylic acids
Alternative Parents Monocarboxylic acids and derivatives  Organic oxides  Organic nitrogen compounds  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Monocarboxylic acid or derivatives - Carboxylic acid - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
설명This compound belongs to the class of organic compounds known as carboxylic acids. These are compounds containing a carboxylic acid group with the formula -C(=O)OH.
External Descriptors ammonium salt
3D 구조
상호 작용 화학 구조 모델





인증서(CoA, COO, BSE/TSE 및 분석 차트)
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.

2 results found

Lot NumberCertificate Type날짜항목
A2628678A2628678Certificate of AnalysisFeb 27, 2026 A432862
L2405618L2405618Certificate of AnalysisDec 16, 2024 A432862
화학 및 물리적 특성
용해성H2O: 10M at20°C, clear, colorless
녹는점(°C)116°C
분자량63.056 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass63.032 Da
Monoisotopic Mass63.032 Da
Topological Polar Surface Area41.100 Ų
Heavy Atom Count4
Formal Charge0
Complexity7.500
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 Count2
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Methodological Studies on Glycoprotein Structural Characterization and Quality Attribute Analysis
Understanding Cbz (Benzyloxycarbonyl): Selection Logic and Practical Value of a Classical Amino Protecting Group
From the Logic of Deprotection to Protecting Group Choice: Differences Among Bn, PMB, and Dmb in Experimental Design
Research Framework for Multi-Enzyme Digestion Strategies and Optimization of Proteomic Coverage
Technical Comparison and Method Selection for Hydroxyproline Determination
Experimental Assessment of Dibenzyl N,N-Diisopropylphosphoramidite for Alcohol O-Phosphorylation: Coupling, Oxidation, and Debenzylation
Porous Graphitic Carbon (PGC) Chromatography Columns: Creating New Selectivity for Challenging Separations through Molecular Shape and the π-Electron Cloud on the Graphitic Surface
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Citations of This Product
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