Palmitic acid - BioReagent, ≥99% , CAS No.57-10-3

CAS: 57-10-3 Cat. No.: P755719 분자식: C16H32O2 분자량: 256.42 Beilstein Registry Number: 607489 EC 번호: 200-312-9
주문 가능
GRADE & PURITY BioReagent ? BioReagent grade — tested suitable for life-science and molecular-biology use. Use for cell culture, assays, and biochemical work needing biological compatibility. ≥99%
Synonyms
1-Pentadecanecarboxylic acid | Cetylic acid | Hexadecanoic acid | NSC 5030 | PamOH
Storage
Room temperature
Shipped In
Normal
★
Size
USA
독일 (EU)*
Price
Qty
5g
P755719-5g
주문제작 · 8~12주
US$63.90
25g
P755719-25g
주문제작 · 8~12주
US$249.90
Enter a quantity for the sizes you want to add.
🧪
Why this grade

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

🌡

Storage & shipping

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

📋

Quality documents

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

📚

Literature proof

Cited in 241 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

개요

Palmitic acid has been used:

  • as a medium supplement in chorionic villous tissue culture form placenta
  • as a component of hormone pellet for implantation in mice ovary
  • for inducing expression of immunity-related GTPase M (IRGM) in human monocytic cell line, THP-1


Specifications

동의어
1-Pentadecanecarboxylic acid | Cetylic acid | Hexadecanoic acid | NSC 5030 | PamOH
사양 및 순도
BioReagent, ≥99%
생화학 및 생리적 메커니즘
Palmitic acid (PA) is a component of membrane phospholipids (PL) and adipose triacylglycerols (TAG). Elevated levels of palmitic acid contributes to the pathophysiology of atherosclerosis, type 2 diabetes mellitus, neurodegenerative diseases, obesity and
보관 조건
Room temperature
배송
Normal
등급
BioReagent
순수함
≥99%
이름과 식별자
정식 스마일
CCCCCCCCCCCCCCCC(=O)O
IUPAC Name
hexadecanoic acid
InChIKey
IPCSVZSSVZVIGE-UHFFFAOYSA-N
INCHI
1S/C16H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h2-15H2,1H3,(H,17,18)
이성체 SMILES
CCCCCCCCCCCCCCCC(=O)O
WGK 독일
3
RTECS
RT4550000
대체 CAS
57-10-3
NSC 번호
5030
MeSH 용어
Acid, Hexadecanoic;Acid, Palmitic;Calcium Palmitate;Hexadecanoic Acid;Palmitate, Calcium;Palmitate, Sodium;Palmitic Acid;Sodium Palmitate
분자량
256.42
Beilstein
607489
Reaxy-Rn
607489
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=607489&ln=

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
SuperclassLipids and lipid-like molecules
분류Fatty Acyls
SubclassFatty acids and conjugates
Intermediate Tree Nodes Not available
Direct ParentLong-chain fatty acids
Alternative Parents Straight chain fatty acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Long-chain fatty acid - Straight chain fatty acid - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - 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 long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.
External Descriptors Straight chain fatty acids
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.

7 results found

Lot NumberCertificate Type날짜항목
H2618460Certificate of AnalysisAug 13, 2026 P755719
H2618461Certificate of AnalysisAug 13, 2026 P755719
A2619526Certificate of AnalysisDec 31, 2025 P755719
A2622613Certificate of AnalysisDec 31, 2025 P755719
A2622614Certificate of AnalysisDec 31, 2025 P755719
C2619592Certificate of AnalysisDec 31, 2025 P755719
E2626129Certificate of AnalysisDec 31, 2025 P755719
화학 및 물리적 특성
용해성chloroform: 0.5 M, clear, colorless
굴절률1.4273
발화점(°F)235.4 °F
발화점(°C)113℃
끓는점(°C)271.5°C
녹는점(°C)62°C
분자량256.420 g/mol
XLogP36.400
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count14
Exact Mass256.24 Da
Monoisotopic Mass256.24 Da
Topological Polar Surface Area37.300 Ų
Heavy Atom Count18
Formal Charge0
Complexity178.000
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
자주 묻는 질문과 기사
HepG2 Cell Steatosis Model Establishment Protocol
Fatty Acids from Basics to Lab Practice: Structural Classification, Research Uses, and Selection Tips (with an Aladdin Representative Product Quick-Reference Table)
Review of the Principles, Common Methods, and Key Application Considerations for the Determination of Glycerol and Triglyceride Contents
Review of the Structural Characteristics, Biological Functions, and Application Advances of Lycopene
Revisiting Titanium Tetrachloride: New Advances in the Direct Amidation and Esterification of Carboxylic Acids
DAST-Mediated Amidation at Room Temperature: Method Features, Practical Value, and Scope of Applicability
Central–Peripheral Signaling Networks Regulated by Neuropeptides and the Integration of Energy Metabolism
Acetyl-Group Metabolic Enzyme Network and In Vitro Enzymology Analysis
mtDNA Stress and cGAS–STING/AIM2 Innate Immune Activation Mediated by CRAT Deficiency
Why Do Cancer Cells Synthesize Their Own Fatty Acids? From the De Novo Fatty Acid Synthesis Pathway to Experimental Assessment
Potassium Fatty Acid Soaps: Structure and Formulation Applications—Production Processes, Alkalinity, Foam Control, and Low-Foam Cleaning
What Is the Difference Between Triethanolamine and Diethanolamine: Understanding Their Formulation Functions, Application Differences, and Selection Logic from a Molecular-Structure Perspective
Why Can 6501 (Cocamide DEA) Stabilize Foam and Build Viscosity? Structural Mechanism, 1:1/1:1.5 Differences, and Application Selection
Differences, Functions, and Selection Guidelines for Sodium Hydroxide Flakes, Granules, Liquid Caustic Soda, and Caustic Soda in Household and Personal Care Product Manufacturing: The Functional and Application Logic of Sodium Hydroxide
From Structure to Selection: Mechanisms and Application Assessment of Low-Foam Oil and Wax Removal with Fatty Acid Methyl Ester Ethoxylates (FMEE)
Mechanism of Action and Selection Logic of Defoamers for Daily Chemical Products: Foam Stability, Foam-Breaking Mechanisms, and Representative Raw Material Analysis
Understanding Anionic Surfactants in Household and Personal-Care Formulations from a Structural Perspective: Structural and Performance Differences among Representative Raw Materials such as LAS, AES, K12, AOS, MES, and FMES
Understanding Ceramides from the Perspective of the Stratum Corneum Lipid Barrier: Moisturizing and Barrier-Repair Mechanisms, Ingredient Selection, and Formulation Research Considerations
Establishment and Evaluation Methods of Diabetic Animal Models
β-Hydroxybutyrate Detection Methods and Metabolic Significance: Comparative Applications of Enzymatic Assays, Blood Ketone Meters, and LC-MS
Mechanistic Analysis of Topical Glutathione in Skincare: Cellular Redox Regulation, Skin Delivery Challenges, and SLN-Based Delivery Strategies
Applications of Endocrinology/Hormones in Metabolic Regulation, Reproductive Function, and Disease Research
Protective and Potential Reparative Mechanisms of Prinsepia utilis Seed Oil on the Skin Barrier: Fatty Acid Composition, Epidermal Lipid Metabolism, and Research Evidence
Structure, Stratum Corneum Distribution, and Stratum Corneum Conditioning Mechanism of Capryloyl Salicylic Acid: Barrier Effects and Safety Evaluation
Regulatory Mechanisms, Research Methods, and Modification-Omics Analysis of Protein Post-Translational Modifications
Regulatory Mechanisms, Research Methods, and Modification-Omics Analysis of Protein Post-Translational Modifications
Potential Mechanisms of Tea Polyphenols in Oily, Acne-Prone Skin: Effects of EGCG on Sebum Production, Lipid Peroxidation, and Inflammatory Responses
Gentiana Root Extract and Gentiopicroside: Chemical Composition, Antioxidant and Inflammation-Modulating Mechanisms, and Their Potential Effects on Skin Barrier Homeostasis
The Sebum-Regulating Potential of Zinc PCA and Its Relationship with Stratum Corneum Hydration
Mechanisms by Which Fructan-Rich Ophiopogon japonicus Tuberous Root Extract Supports Skin Moisturization and Barrier Function
How Palmitoyl Pentapeptide-4 Acts on the Skin: From the KTTKS Sequence and Skin Delivery to Collagen Matrix Responses
The Logic of Biomimetic Peptide Action in Skin: Sequence and Conformation, Skin Delivery, Stability, and Target Matching
Antidiabetic Mechanisms, Representative Bioactive Compounds, and Research Applications of Natural Products
The Combination Logic of Palmitoyl Tripeptide-1 and Palmitoyl Pentapeptide-4: Skin Delivery, Matrix Signaling, and Regulation of Collagen Homeostasis
How Ectoine Regulates Skin Hydration: Zwitterionic Structure, Preferential Hydration, and Barrier-Support Mechanisms
Molecular Mechanisms by Which Natural Products Regulate Adipose Browning
Are Lipids Fats? Understanding the Multiple Functions of Lipids from Cellular Metabolism to mRNA Delivery
Bakuchiol Is Not “Plant Retinol”: Chemical Structure, Anti-Aging Mechanisms, and Functional Similarities and Differences Compared with Retinol
Structure, Emollient and Moisturizing Effects, and Source Identification of Squalane: From Complete Hydrogenation of Squalene to Stable Isotope Analysis
Why Do Skincare Oligopeptides Have Different Effects? — Molecular Structure, Skin Delivery, and Mechanisms of Action
Stratum Corneum Penetration and Skin Mechanisms of Panthenol: Moisturization, Barrier Repair, and Soothing Effects
Citations of This Product
솔루션 계산기
리뷰

고객 리뷰

자주 묻는 질문

What is the purity of this product?
This product is supplied at ≥99% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.
What does BioReagent mean?
BioReagent indicates that the product has been processed and tested for biological and biochemical applications. Specifications may include endotoxin limits, microbial controls, sterility, low DNase/RNase/protease activity, and verified biological activity where relevant.
How should this product be stored?
Store at room temperature.
How is this product shipped?
This product ships under standard ambient conditions. No temperature-controlled packaging is required.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 57-10-3, the molecular formula is C16H32O2, and the molecular weight is 256.42 g/mol. InChIKey IPCSVZSSVZVIGE-UHFFFAOYSA-N.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

Need help choosing the grade?

Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.

View BioReagent grade guide →

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.