6-Hydroxyhexanoic acid - ≥95% , CAS No.1191-25-9

Name: 6-Hydroxyhexanoic acid - ≥95% , CAS No.1191-25-9
SKU: H302536
Availability: InStock

CAS: 1191-25-9 Cat. No.: H302536 Formule: C₆H₁₂O₃ Poids moléculaire: 132.16 Numéro CE: 681-173-5

COA

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6-Hydroxyhexanoic acid - ≥95% CAS No(1191-25-9) by Aladdin Scientific

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DISPONIBLE À COMMANDE

GRADE & PURITY ≥95%

Synonyms

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Vue d’ensemble Specifications Noms et identifiants Documentation Advanced Data Taxonomic Classification Structure 3D Cibles associées (humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Calculateurs de solution Avis

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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

Product Application：

6-Hydroxyhexanoic acid acts as a useful reagent in synthetic chemistry. It is used as a precursor to prepare surface active monomers.

Specifications

Synonymes

Spécifications et pureté

≥95%

Conditions de stockage de stockage

Store at -20°C

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Pureté

≥95%

Noms et identifiants

Pubchem Sid	508810207
Sourires canoniques	C(CCC(=O)O)CCO
IUPAC Name	6-hydroxyhexanoic acid
InChIKey	IWHLYPDWHHPVAA-UHFFFAOYSA-N
INCHI	1S/C6H12O3/c7-5-3-1-2-4-6(8)9/h7H,1-5H2,(H,8,9)
Isomères SMILES	C(CCC(=O)O)CCO
Poids moléculaire	132.16
Reaxy-Rn	1236785
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1236785&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

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Classe Hydroxy acids and derivatives
    - Subclass Medium-chain hydroxy acids and derivatives

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Classe	Hydroxy acids and derivatives
Subclass	Medium-chain hydroxy acids and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Medium-chain hydroxy acids and derivatives
Alternative Parents	Medium-chain fatty acids Hydroxy fatty acids Straight chain fatty acids Monocarboxylic acids and derivatives Carboxylic acids Primary alcohols Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Medium-chain hydroxy acid - Medium-chain fatty acid - Hydroxy fatty acid - Straight chain fatty acid - Fatty acyl - Fatty acid - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Carbonyl group - Organic oxide - Organic oxygen compound - Alcohol - Organooxygen compound - Primary alcohol - Hydrocarbon derivative - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as medium-chain hydroxy acids and derivatives. These are hydroxy acids with a 6 to 12 carbon atoms long side chain.
External Descriptors	Hydroxy fatty acids
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

Structure 3D

Cibles associées (humaines)

A498 (42825 Activities)

Lot Number	Certificate Type	Date	Article
H2505081	Certificate of Analysis	Aug 20, 2025	H302536
B2209476	Certificate of Analysis	Dec 12, 2024	H302536
B2209665	Certificate of Analysis	Dec 12, 2024	H302536
B2209670	Certificate of Analysis	Dec 12, 2024	H302536
K2421455	Certificate of Analysis	Apr 13, 2024	H302536
B2209489	Certificate of Analysis	Jan 14, 2022	H302536
B2328176	Certificate of Analysis	Jan 14, 2022	H302536
F2425122	Certificate of Analysis	Jan 14, 2022	H302536
F2506094	Certificate of Analysis	Jan 14, 2022	H302536
G2416061	Certificate of Analysis	Jan 14, 2022	H302536
H2514160	Certificate of Analysis	Jan 14, 2022	H302536
I2518036	Certificate of Analysis	Jan 14, 2022	H302536

Sensibilité	Hygroscopic
Indice de réfraction	1.456
Point d'éclair (°F)	230°F
Point d'éclair (°C)	>110°
Point d'ébullition (°C)	113-116℃
Point de fusion (°C)	38-40°
Poids moléculaire	132.160 g/mol
XLogP3	-0.400
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	5
Exact Mass	132.079 Da
Monoisotopic Mass	132.079 Da
Topological Polar Surface Area	57.500 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	80.400
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