N-(Hydroxymethyl)phthalimide - ≥98% , CAS No.118-29-6

CAS: 118-29-6 Cat. No.: N124077 Peso molecular: 177.16 Beilstein Registry Number: 140946 Número EC: 204-241-4
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
AI3-28943 | CHEBI:38816 | Hydroxymethylphthalimide | N-(Hydroxymethyl)phthalimide, 97% | STR02558 | PHTHALIMIDE, N-(HYDROXYMETHYL)- | AC-19446 | NCGC00258413-01 | SCHEMBL101555 | DTXSID1026954 | NSC27471 | NSC-27471 | F0777-0575 | Phthalimidomethyl alcoho
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25g
N124077-25g
8
9,90US$
100g
N124077-100g
3
10,90US$
250g
N124077-250g
3

17,90US$

26,90US$
Guardar 9,00 US$ (33.46%)
500g
N124077-500g
2

27,90US$

41,90US$
Guardar 14,00 US$ (33.41%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% 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.

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Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Safe reagent for the in situ generation of anhydrous formaldehyde in organic solvents
For amidomethylation of aromatics in triflic acid.

Specifications

Sinónimos
AI3-28943 | CHEBI:38816 | Hydroxymethylphthalimide | N-(Hydroxymethyl)phthalimide, 97% | STR02558 | PHTHALIMIDE, N-(HYDROXYMETHYL)- | AC-19446 | NCGC00258413-01 | SCHEMBL101555 | DTXSID1026954 | NSC27471 | NSC-27471 | F0777-0575 | Phthalimidomethyl alcoho
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488180760
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180760
Sonrisas canónicasC1=CC=C2C(=C1)C(=O)N(C2=O)CO
IUPAC Name2-(hydroxymethyl)isoindole-1,3-dione
InChIKeyMNSGOOCAMMSKGI-UHFFFAOYSA-N
INCHI1S/C9H7NO3/c11-5-10-8(12)6-3-1-2-4-7(6)9(10)13/h1-4,11H,5H2
Isómeros SMILES C1=CC=C2C(=C1)C(=O)N(C2=O)CO
WGK Alemania 3
RTECS TI5270000
Peso molecular 177.16
Beilstein 140946
Reaxy-Rn 140946
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=140946&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
SuperclassOrganoheterocyclic compounds
ClaseIsoindoles and derivatives
SubclassIsoindolines
Intermediate Tree Nodes Isoindolones
Direct ParentPhthalimides
Alternative Parents Isoindoles  N-substituted carboxylic acid imides  Benzenoids  Azacyclic compounds  Alkanolamines  Organopnictogen compounds  Organooxygen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Phthalimide - Isoindole - Carboxylic acid imide, n-substituted - Benzenoid - Carboxylic acid imide - Azacycle - Alkanolamine - Carboxylic acid derivative - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as phthalimides. These are aromatic heterocyclic compounds containing a 1,3-dioxoisoindoline moiety. They are imide derivatives of phthalic anhydrides.
External Descriptors primary alcohol - phthalimides
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

10 results found

Lot NumberCertificate TypeFechaArticulo
H2206168Certificate of AnalysisMay 20, 2026 N124077
H2206169Certificate of AnalysisMay 20, 2026 N124077
A2113124Certificate of AnalysisNov 14, 2024 N124077
A2113126Certificate of AnalysisNov 14, 2024 N124077
K2504780Certificate of AnalysisApr 28, 2024 N124077
K2504781Certificate of AnalysisApr 28, 2024 N124077
D2323869Certificate of AnalysisMar 10, 2023 N124077
G1501105Certificate of AnalysisMar 10, 2023 N124077
H2206167Certificate of AnalysisJun 15, 2022 N124077
K2425030Certificate of AnalysisJun 15, 2022 N124077
Propiedades químicas y físicas
Punto de fusión (°C)147.0°C
Peso molecular177.160 g/mol
XLogP31.500
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass177.043 Da
Monoisotopic Mass177.043 Da
Topological Polar Surface Area57.600 Ų
Heavy Atom Count13
Formal Charge0
Complexity227.000
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
Citations of This Product
Referencias
1. Wang Yifan, Dong Wenjian, Yan Xuefeng, Li Xia, Yu Liangmin.  (2025)  Synthesis and antifouling properties of carbazole amide derivatives with fluorescent functional structure.  JOURNAL OF MATERIALS SCIENCE,      [PMID:] [10.1007/s10853-025-10725-9]
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