CAS 828272-19-1 SDS Request & Safety Reference

Preliminary reference disclaimer

This preliminary safety reference is generated from structured MolGraph catalog fields and public reference-style data. It is not a supplier-issued Safety Data Sheet and should not be used as a substitute for supplier-issued documentation, workplace safety review, transport classification, or regulatory compliance decisions. For supplier SDS or COA, submit a documentation request through MolGraph.

Documentation status

Preliminary safety reference

Available

Supplier-issued SDS

Available by request

COA

Available by RFQ / lot confirmation

Transport classification

Requires shipment review

Identity

CAS Number

828272-19-1

Chemical name

tert-butyl N-(3-bromopropyl)-N-methylcarbamate

Molecular formula

C9H18BrNO2

Molecular weight

252.15 g/mol

Synonyms

824-763-1; 3-Bromo-N-methyl-N-boc-propylamine; tert-Butyl (3-bromopropyl)(methyl)carbamate; Carbamic acid, (3-bromopropyl)methyl-, 1,1-dimethylethyl ester; N-Boc-N-methyl-3-bromopropylamine; tert-Butyl (3-bromopropyl)methylcarbamate; t-Butyl (3-bromopropyl)(methyl)carbamate; tert-Butyl(3-bromopropyl)(methyl)carbamate; C77502; tert-butyl N-(3-bromopropyl)-N-methyl-carbamate; F621539

InChIKey

PIUWBRCCWDAPFG-UHFFFAOYSA-N

PubChem CID

46780899

Hazard / GHS Reference

GHS Pictograms

Catalog reference cue; confirm supplier documentation before use.

Handling & PPE

Handle in a well-ventilated area or fume hood.
Avoid inhalation of vapor or mist, and avoid contact with skin and eyes.
Keep container tightly closed in a dry and well-ventilated place.
Store away from incompatible materials.
Wear appropriate protective equipment including a lab coat, chemical-resistant gloves, and eye protection (safety goggles).
Use respiratory protection if ventilation is inadequate or if there is a risk of exposure to dust or aerosols.
Ensure that eyewash stations and safety showers are close to the workstation location.
Wash contaminated clothing before reuse.
Dispose of contents and container in accordance with local, regional, national, and international regulations.

First Aid / Accidental Release

In case of skin contact, wash off with soap and plenty of water. Seek medical attention if irritation persists.
In case of eye contact, rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Seek medical attention.
If inhaled, move to fresh air. If not breathing, give artificial respiration. Seek medical attention.
If swallowed, rinse mouth with water. Do NOT induce vomiting. Seek medical attention immediately.
Evacuate personnel to safe areas and keep unnecessary personnel away.
Avoid dust or aerosol generation. Do not breathe dust, vapors, mist, or gas.
For spills, collect material using an inert absorbent and place in a suitable disposal container.
Ensure adequate ventilation during cleanup. Refer to institutional spill response procedures.
Dispose of contents and container in accordance with local, regional, national, and international regulations.

Firefighting / Stability

Use water spray, alcohol-resistant foam, dry chemical, or carbon dioxide for extinguishing.
Wear self-contained breathing apparatus for firefighting if necessary.
Keep containers cool with water spray.
Prevent firefighting water from entering drains or water courses.
This product is generally considered stable under recommended storage conditions.
Avoid strong oxidizing agents, strong acids, and strong bases.
May decompose upon heating, releasing irritating or toxic fumes.
No known hazardous reactions under normal conditions of use.

Physical and Chemical Reference

Appearance

Colorless to pale yellow liquid

Catalog reference value; verify against supplier SDS before use.

Physical State

Liquid

Catalog reference value; verify against supplier SDS before use.

Melting Point

-5

Catalog reference value; verify against supplier SDS before use.

Boiling Point

241.0 °C

Catalog reference value; verify against supplier SDS before use.

Density

1.23 g/cm³

Catalog reference value; verify against supplier SDS before use.

Water Solubility

Slightly soluble

Catalog reference value; verify against supplier SDS before use.

Flash Point

110.1 °C

Catalog reference value; verify against supplier SDS before use.

Vapor Pressure

Estimated value, unit not specified

Catalog reference value; verify against supplier SDS before use.

Autoignition Temp

350.0 °C

Catalog reference value; verify against supplier SDS before use.

Transport / Shipment Review

HS Code

29241990

Preliminary catalog cue; verify before compliance decisions.

GHS Pictograms

Preliminary catalog cue; verify before compliance decisions.

Compliance

standard-ruo

Preliminary catalog cue; verify before compliance decisions.

Registration Status

DSL: pending; AICS: pending; ENCS: pending; ICSR: pending; TSCA: pending; IECSC: pending; INSQR: pending; REACH: pending; K-REACH: pending; SEA_Regulatory: pending

Registration values are catalog reference status cues and may require jurisdiction-specific review.

Shipment review

Shipment details require review before fulfillment.

Transport classification must be confirmed using supplier SDS and shipment documentation before dispatch.

Transport classification must be confirmed using supplier SDS and shipment documentation before dispatch.

Need supplier documentation?

Request through MolGraph:

Supplier-issued SDS
COA
Purity and pack size confirmation
Availability and lead time review
Shipment documentation review

Catalog-Specific Reference Cues

tert-butyl N-(3-bromopropyl)-N-methylcarbamate is a Boc-protected methylamine derivative featuring a 3-bromopropyl chain. This compound serves as a versatile research chemical, primarily utilized as a building block or intermediate in organic synthesis.
tert-butyl N-(3-bromopropyl)-N-methylcarbamate, with CAS 828272-19-1 and molecular formula C9H18BrNO2, is a functionalized carbamate. Its structure incorporates a tert-butyl carbamate (Boc) protecting group on a methylamine, which is further substituted with a 3-bromopropyl chain. This combination makes it a valuable intermediate in synthetic organic chemistry. Researchers may employ this compound for introducing protected methylamino-propyl functionalities, participating in nucleophilic substitution reactions via the bromo group, or for subsequent deprotection and further derivatization. It is intended for Research Use Only (RUO).
This compound is primarily used in organic synthesis as a versatile building block. Its applications include the introduction of protected methylamino-propyl groups, participation in various coupling reactions, and as an intermediate for synthesizing more complex molecules in academic and industrial research settings.

Related catalog entries

(3-Bromo-1-methylpropyl)carbamic acid tert-butyl esterView related compound →tert-butyl N-(1-bromobutan-2-yl)carbamateView related compound →tert-butyl N-(3-bromo-2-methylpropyl)carbamateView related compound →tert-butyl N-(3-bromobutyl)carbamateView related compound →tert-butyl N-[(2S)-4-bromobutan-2-yl]carbamateView related compound →

Identity

CAS Number

828272-19-1

Chemical name

tert-butyl N-(3-bromopropyl)-N-methylcarbamate

Molecular formula

C9H18BrNO2

Molecular weight

252.15 g/mol

Synonyms

InChIKey

PIUWBRCCWDAPFG-UHFFFAOYSA-N

PubChem CID

46780899

Handling & PPE

Handle in a well-ventilated area or fume hood.
Avoid inhalation of vapor or mist, and avoid contact with skin and eyes.
Keep container tightly closed in a dry and well-ventilated place.
Store away from incompatible materials.
Wear appropriate protective equipment including a lab coat, chemical-resistant gloves, and eye protection (safety goggles).
Use respiratory protection if ventilation is inadequate or if there is a risk of exposure to dust or aerosols.
Ensure that eyewash stations and safety showers are close to the workstation location.
Wash contaminated clothing before reuse.
Dispose of contents and container in accordance with local, regional, national, and international regulations.

First Aid / Accidental Release

In case of skin contact, wash off with soap and plenty of water. Seek medical attention if irritation persists.
In case of eye contact, rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Seek medical attention.
If inhaled, move to fresh air. If not breathing, give artificial respiration. Seek medical attention.
If swallowed, rinse mouth with water. Do NOT induce vomiting. Seek medical attention immediately.
Evacuate personnel to safe areas and keep unnecessary personnel away.
Avoid dust or aerosol generation. Do not breathe dust, vapors, mist, or gas.
For spills, collect material using an inert absorbent and place in a suitable disposal container.
Ensure adequate ventilation during cleanup. Refer to institutional spill response procedures.
Dispose of contents and container in accordance with local, regional, national, and international regulations.

Firefighting / Stability

Use water spray, alcohol-resistant foam, dry chemical, or carbon dioxide for extinguishing.
Wear self-contained breathing apparatus for firefighting if necessary.
Keep containers cool with water spray.
Prevent firefighting water from entering drains or water courses.
This product is generally considered stable under recommended storage conditions.
Avoid strong oxidizing agents, strong acids, and strong bases.
May decompose upon heating, releasing irritating or toxic fumes.
No known hazardous reactions under normal conditions of use.

Physical and Chemical Reference

Appearance

Colorless to pale yellow liquid

Catalog reference value; verify against supplier SDS before use.

Physical State

Liquid

Catalog reference value; verify against supplier SDS before use.

Melting Point

-5

Catalog reference value; verify against supplier SDS before use.

Boiling Point

241.0 °C

Catalog reference value; verify against supplier SDS before use.

Density

1.23 g/cm³

Catalog reference value; verify against supplier SDS before use.

Water Solubility

Slightly soluble

Catalog reference value; verify against supplier SDS before use.

Flash Point

110.1 °C

Catalog reference value; verify against supplier SDS before use.

Vapor Pressure

Estimated value, unit not specified

Catalog reference value; verify against supplier SDS before use.

Autoignition Temp

350.0 °C

Catalog reference value; verify against supplier SDS before use.

Transport / Shipment Review

HS Code

29241990

Preliminary catalog cue; verify before compliance decisions.

GHS Pictograms

Preliminary catalog cue; verify before compliance decisions.

Compliance

standard-ruo

Preliminary catalog cue; verify before compliance decisions.

Registration Status

DSL: pending; AICS: pending; ENCS: pending; ICSR: pending; TSCA: pending; IECSC: pending; INSQR: pending; REACH: pending; K-REACH: pending; SEA_Regulatory: pending

Registration values are catalog reference status cues and may require jurisdiction-specific review.

Shipment review

Shipment details require review before fulfillment.

Transport classification must be confirmed using supplier SDS and shipment documentation before dispatch.

Transport classification must be confirmed using supplier SDS and shipment documentation before dispatch.

Catalog-Specific Reference Cues

tert-butyl N-(3-bromopropyl)-N-methylcarbamate is a Boc-protected methylamine derivative featuring a 3-bromopropyl chain. This compound serves as a versatile research chemical, primarily utilized as a building block or intermediate in organic synthesis.
tert-butyl N-(3-bromopropyl)-N-methylcarbamate, with CAS 828272-19-1 and molecular formula C9H18BrNO2, is a functionalized carbamate. Its structure incorporates a tert-butyl carbamate (Boc) protecting group on a methylamine, which is further substituted with a 3-bromopropyl chain. This combination makes it a valuable intermediate in synthetic organic chemistry. Researchers may employ this compound for introducing protected methylamino-propyl functionalities, participating in nucleophilic substitution reactions via the bromo group, or for subsequent deprotection and further derivatization. It is intended for Research Use Only (RUO).
This compound is primarily used in organic synthesis as a versatile building block. Its applications include the introduction of protected methylamino-propyl groups, participation in various coupling reactions, and as an intermediate for synthesizing more complex molecules in academic and industrial research settings.

CAS 828272-19-1 Safety Reference and Supplier SDS Request

Documentation status

Identity

Hazard / GHS Reference

Handling & PPE

First Aid / Accidental Release

Firefighting / Stability

Physical and Chemical Reference

Transport / Shipment Review

CAS 828272-19-1 Safety Reference and Supplier SDS Request

Documentation status

Identity

Hazard / GHS Reference

Handling & PPE

First Aid / Accidental Release

Firefighting / Stability

Physical and Chemical Reference

Transport / Shipment Review