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Nitrobenzoic Acid · CAS 62-23-7

Para Nitrobenzoic Acid

C7H5NO4 Molar mass 167.12 g/mol

Para Nitrobenzoic Acid is the documented precursor to procaine and to para-aminobenzoic acid (PABA), itself a folic-acid synthesis intermediate — a long-established pharmaceutical building block made by oxidation of 4-nitrotoluene, not nitration of benzoic acid.

Identification Sheet REP.
IUPAC name4-Nitrobenzoic acid
CAS number62-23-7
EC / EINECS numberNot found as a classic EINECS number (ECHA InfoCard 100.000.479)
Molecular formulaC₇H₅NO₄
Molar mass167.12 g/mol
AppearanceLight-yellow crystalline powder
Common synonyms4-Nitrobenzoic acid, PNBA
Melting Point237 °Csolid, well above ambient
Boiling PointSublimesdoes not boil in the normal sense
Density~1.58 g/cm³at 20 °C
Water Solubility<0.1 g/100 mLat 26 °C, poorly soluble
Purity Offered98% / 99%technical & high-purity grades
01 / PRODUCT DOSSIER

What Para Nitrobenzoic Acid is, and why buyers source it

A working overview of the compound's chemistry, its place in the aniline-derivative family, and the grades Chelora Chemicals keeps in regular supply.

Para Nitrobenzoic Acid (PNBA) is a simple, well-characterised aromatic compound: a nitro group and a carboxylic acid group positioned opposite each other on the benzene ring. We want to correct a plausible-sounding assumption directly: the documented industrial route to this compound is oxidation of 4-nitrotoluene, not nitration of plain benzoic acid — the two routes would give the same product in principle, but the nitrotoluene oxidation route is the one actually used at scale.

Its real, documented pharmaceutical-chain significance is as a precursor, via its acid chloride, to procaine (a classic local anesthetic), and separately as a route to para-aminobenzoic acid (PABA) by reduction of the nitro group — PABA itself being a documented intermediate in folic acid (vitamin B9) synthesis. Dye-intermediate use is commonly claimed by suppliers in the trade, but we were not able to independently confirm a specific, documented dye-chemistry application in primary sources, so we note that claim honestly as supplier-reported rather than independently verified.

Where it fits in the synthesis chain

We supply Para Nitrobenzoic Acid itself. We do not manufacture or supply procaine, PABA, folic acid, or any other finished pharmaceutical product made from it.

Grades we supply

98% and 99% grades are both seen across the trade; pharmaceutical-intermediate buyers typically specify the higher grade.

02 / MANUFACTURING ROUTE

How Para Nitrobenzoic Acid is made

An overview of the production route for orientation purposes. Our manufacturing partners' own process parameters and in-process controls are proprietary and are not disclosed beyond what is needed to interpret the certificate of analysis.

Para Nitrobenzoic Acid is made industrially by oxidation of 4-nitrotoluene, using either oxygen under catalytic conditions or a dichromate oxidant, converting the methyl group directly to the carboxylic acid while leaving the nitro group untouched.

This oxidation route is the documented industrial process — we want to be clear that nitration of benzoic acid itself, while chemically plausible as an alternative on paper, is not the route actually used at scale for this compound, and we correct that assumption here rather than let it stand unchallenged.

The crude product is purified by crystallisation, taking advantage of its high melting point and low water solubility to separate it cleanly from unreacted starting material and over-oxidised by-products before drying to the finished powder.

A route correction worth making explicit

It would be reasonable to assume this compound is made by nitrating benzoic acid directly, since that mirrors how several other nitro-substituted building blocks in the broader trade are made. The documented industrial process for this specific compound is different: oxidation of 4-nitrotoluene's methyl group to the carboxylic acid. We state the correct, documented route rather than the plausible-sounding alternative.

03 / APPLICATIONS

Industries and processes that use it

Para Nitrobenzoic Acid is consumed almost entirely as a synthesis intermediate. The four fields below account for most of the demand we see through our export desk.

Field 01

Procaine & Local Anesthetic Synthesis

Via its acid chloride, this compound is a documented precursor in the synthesis of procaine, a classic local anesthetic.

Field 02

PABA & Folic Acid Synthesis Chain

Reduction of the nitro group gives para-aminobenzoic acid (PABA), itself a documented intermediate in folic acid (vitamin B9) synthesis.

Field 03

General Fine-Chemical Intermediate

Used more broadly as a building block in fine-chemical synthesis wherever this specific nitro/carboxylic-acid substitution pattern is required; dye-intermediate use is commonly claimed by suppliers but was not independently confirmed in the sources we checked.

04 / REACTION CHEMISTRY

How the molecule is typically carried forward

Para Nitrobenzoic Acid offers two independent reactive handles: the carboxylic acid, activated to its acid chloride for further synthesis, and the nitro group, reduced when the target is the corresponding amine.

Acid chloride formation

Reaction with thionyl chloride or a similar reagent converts the carboxylic acid to the corresponding acid chloride, the activated form used in procaine synthesis and other acylation chemistry.

Reduction of the nitro group

Catalytic or chemical reduction converts the nitro group to an amine, giving para-aminobenzoic acid (PABA), the documented folic-acid-chain intermediate.

Amide formation

Reaction with ammonia or an amine, via the acid chloride, gives the corresponding amide — the same general chemistry used to make Para Nitrobenzamide, the related product elsewhere in this part of our range.

05 / FAMILY COMPARISON

Para Nitrobenzoic Acid against its near relatives

Para Nitrobenzoic Acid and Para Nitrobenzamide are the two nitrobenzene-derivative intermediates in this part of our range, related as acid and amide forms of the same core structure.

ProductCAS NumberTypically Used InNotes
Para Nitrobenzoic Acid62-23-7Procaine and PABA/folic acid synthesis chainThe product on this page.
Para Nitrobenzamide619-80-7Pharmaceutical and fine-chemical intermediateAlso supplied — see its product page.

Exact physical constants and purity specifications are confirmed per batch on the certificate of analysis — treat the notes above as a sourcing guide rather than a specification sheet.

06 / HAZARD & HANDLING

Safety classification at a glance

Based on GHS classification as commonly listed for this substance. This is a summary for orientation only — always work from the current safety data sheet supplied with your specific batch.

H315

Causes skin irritation.

H319

Causes serious eye irritation.

H335

May cause respiratory irritation.

Signal word

Warning

No harmonised EU CLP Annex VI entry was located for this substance. The classification above reflects general irritant self-classification consistent with its acidic, mildly irritant character. IARC has not evaluated this specific compound — we checked specifically, since several related nitro/amino-nitrobenzene isomers do appear in IARC's broader review scope, but this compound itself has not been separately evaluated.

07 / STORAGE & SHELF LIFE

Keeping it on spec between delivery and use

General storage guidance for this grade. Site-specific storage rules, segregation requirements and re-test intervals should follow your own EHS procedures and the MSDS issued with your batch.

Shelf Life24 months, unopened
Storage Temp15–30 °C
ContainerFibre drums or multi-wall paper sacks with polyethylene liner

Store in a cool, dry area away from strong bases and oxidisers, consistent with its character as a carboxylic acid. Keep containers tightly sealed.

08 / PACKING & EXPORT

How it ships from Indonesia

Standard packing and export terms for this product. Confirm exact figures against your order — they vary slightly by destination and quantity.

Standard Packing25 kg bags
Bulk PackingDrums / jumbo bags
Min. OrderFrom 1 drum
Lead Time2 – 4 weeks
Export TermsFOB · CFR · CIF
09 / QUALITY & DOCUMENTATION

What travels with every batch

Specification is agreed before the purchase order, not discovered on arrival. Every shipment of Para Nitrobenzoic Acid leaves with a documented, checkable paper trail.

Doc 01

Certificate of Analysis

Batch-wise assay (by GC), isomer purity, melting point range and moisture, issued against the agreed specification so your QC team can check it, not just file it.

Doc 02

Safety Data Sheet

GHS-format SDS in English covering hazard classification, handling, storage, first-aid and spill response for the exact grade shipped.

Doc 03

Technical Data Sheet

Reference physical and chemical properties, recommended storage and typical applications, for internal circulation to your process or R&D teams.

Doc 04

Certificate of Origin

Confirms Indonesian origin for customs clearance and any preferential-duty claim at your destination port.

Doc 05

Dangerous Goods Declaration

UN packing group, classification and shipper's declaration prepared ahead of loading so documentation never holds up customs.

Doc 06

Third-Party Inspection

Independent pre-shipment inspection and re-sampling can be arranged on request, at your cost, for buyers who require it as a matter of policy.

10 / FAQ

Frequently asked questions

What buyers most often ask our sales desk about this grade.

01What is Para Nitrobenzoic Acid used for?+
Para Nitrobenzoic Acid is used as a pharmaceutical intermediate — via its acid chloride, a documented precursor to procaine, and via nitro-group reduction, a route to para-aminobenzoic acid (PABA), itself a folic acid synthesis intermediate.
02What is the CAS number of Para Nitrobenzoic Acid?+
Its CAS Registry Number is 62-23-7, with EC number Not found as a classic EINECS number (ECHA InfoCard 100.000.479), molecular formula C₇H₅NO₄ and a molar mass of 167.12 g/mol.
03What purity grades does Chelora Chemicals supply?+
We supply technical grade and high-purity grade — the exact figures are shown in the specification rail at the top of this page. Each batch ships with a certificate of analysis stating assay, isomer purity and moisture against the agreed specification.
04Is Para Nitrobenzoic Acid hazardous?+
Yes. It carries the GHS signal word Warning with the hazard statements listed in the hazard section of this page. It should be handled with appropriate PPE and in line with the safety data sheet supplied with each shipment.
05Is this made by nitrating benzoic acid?+
No — we want to correct that plausible-sounding assumption directly. The documented industrial route is oxidation of 4-nitrotoluene's methyl group to the carboxylic acid, not nitration of benzoic acid itself.
06Do you supply procaine, PABA or folic acid directly?+
No. We supply this nitrobenzoic acid intermediate. The acylation chemistry to procaine, and the reduction chemistry to PABA and onward to folic acid, are downstream processes performed by pharmaceutical intermediate manufacturers, not by us.
07Is the dye-intermediate use you sometimes see mentioned for this compound confirmed?+
We looked, and honestly, we could not independently confirm a specific, documented dye-chemistry application for this compound in the primary sources we checked. Some suppliers describe it as a dye intermediate; we report that as a supplier claim rather than a confirmed use.
08What packing options are available?+
Standard packing is 25 kg bags, with drums / jumbo bags available for bulk orders. Trial quantities from a single drum can usually be arranged before you commit to larger volumes.
09How long does delivery take?+
Typical lead time is two to four weeks plus transit, depending on whether the grade is ex-stock or made to order and your destination port. A firm date is confirmed in the written quotation.
10Can I get a sample before placing a bulk order?+
Yes. Pre-shipment samples and a batch certificate of analysis can be arranged so your QC team can verify the specification before committing to volume.
11How is Para Nitrobenzoic Acid manufactured?+
4-Nitrotoluene Oxidation of 4-nitrotoluene (catalytic O2 or dichromate oxidant), converting the methyl group to the carboxylic acid is the usual industrial route, followed by washing and distillation or recrystallisation before packing.
12What is the shelf life, and how should it be stored?+
Typical shelf life is around 24 months in original, unopened packaging stored as described in the storage section of this page. If a batch is held beyond its shelf life, we recommend re-checking assay and moisture before use.
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