Acetate - UPSSS grade, Single metal impurity ≤ 0.01ppb , CAS No.64-19-7

CAS: 64-19-7 Cat. No.: A1523809 Formula: CH3CO2H Molecular Weight: 60.05 Beilstein Registry Number: 506007 EC Number: 200-580-7
AVAILABLE TO ORDER
GRADE & PURITY UPSSS grade ? UPSSS grade — the highest ultra-pure semiconductor tier in this series. Use for the most contamination-sensitive leading-edge processes. Single metal impurity ≤ 0.01ppb
Storage
Room temperature
Shipped In
FedEx DG Service
★
Size
Germany (EU)
USA*
Price
Qty
500ml
A1523809-500ml
Made to order · 8–12 wks
€1,353.59
Enter a quantity for the sizes you want to add.

Specifications

Specifications & Purity
UPSSS grade, Single metal impurity ≤ 0.01ppb
Storage
Room temperature
Shipped In
FedEx DG Service
Grade
UPSSS grade
Names and Identifiers
Canonical Smiles
CC(=O)O
IUPAC Name
acetic acid
InChIKey
QTBSBXVTEAMEQO-UHFFFAOYSA-N
INCHI
1S/C2H4O2/c1-2(3)4/h1H3,(H,3,4)
Isomeric SMILES
CC(=O)O
WGK Germany
1
RTECS
AF1225000
UN Number
2789
Packing Group
II
Molecular Weight
60.05
Beilstein
506007
Reaxy-Rn
506007
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506007&ln=

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassCarboxylic acids
Intermediate Tree Nodes Not available
Direct ParentCarboxylic acids
Alternative Parents Monocarboxylic acids and derivatives  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
DescriptionThis 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 Straight chain fatty acids
Associated Targets(Human)
FFAR2 Tchem Free fatty acid receptor 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
FFAR3 Tchem Free fatty acid receptor 3 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Certificates (CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
SensitivityMoisture Sensitive
x_refractive_index1.37-1.373
x_flash_point_drop_centigrade40℃
x_boil_point_char117-118°C
x_melt_point_char16-16.5°C
Molecular Weight60.050 g/mol
XLogP3-0.200
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass60.0211 Da
Monoisotopic Mass60.0211 Da
Topological Polar Surface Area37.300 Ų
Heavy Atom Count4
Formal Charge0
Complexity31.000
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
FAQs and Articles
Probiotics, Prebiotics, and Postbiotics in Skin Care: Conceptual Distinctions, Mechanisms of Action, and Their Applications in the Care of Dry, Itchy, and Rough Skin
Multilevel Moisturizing Mechanisms of Sodium Hyaluronate and Its Derivatives: Molecular Weight Modulation, Crosslinking, Acetylation, and Major Sites of Action
Sources, Host-Regulatory Mechanisms, and Tumor-Immune Effects of Gut Microbiota-Derived Metabolites
What Determines Collagen Function: From Triple-Helix Formation to Hierarchical Assembly, Crosslink Maturation, and Dynamic Remodeling
Differences Between Animal-Derived Collagen and Recombinant Collagen in Skincare: Sequence and Structure, Safety, Skin Effects, and Evidence Evaluation
3,3-Spiro-α-Proline Building Blocks: Structural Features, Complementary Synthetic Routes, and Multigram-Scale Preparation
Stereoretentive Decarboxylative Amidation with Dioxazolones: A Two-Electron Rearrangement Mechanism for Stereochemical Transfer from Chiral Carboxylic Acids
Desaturative Amination for the Synthesis of Amino Heteroarenes: Carbonyl-Site Predefinition of the C–N Bond-Forming Position and Subsequent Desaturative Aromatization
From Temporary Covalent Assembly to Intramolecular Smiles Aryl Migration: DCPDC-Mediated Phenol–Primary Amine C–N Cross-Coupling
Citations of This Product
Solution Calculators
Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.